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Biol Reprod. 2015 November; 93(5): 112.
Published online 2015 September 23. doi:  10.1095/biolreprod.115.132753
PMCID: PMC5333802

Dynamics of Immune Cell Types Within the Macaque Corpus Luteum During the Menstrual Cycle: Role of Progesterone1

Abstract

The goal of the current study was to characterize the immune cell types within the primate corpus luteum (CL). Luteal tissue was collected from rhesus females at discrete intervals during the luteal phase of the natural menstrual cycle. Dispersed cells were incubated with fluorescently labeled antibodies specific for the immune cell surface proteins CD11b (neutrophils and monocytes/macrophages), CD14 (monocytes/macrophages), CD16 (natural killer [NK] cells), CD20 (B-lymphocytes), and CD3epsilon (T-lymphocytes) for analysis by flow cytometry. Numbers of CD11b-positive (CD11b+) and CD14+ cells increased significantly 3 to 4 days after serum progesterone (P4) concentrations declined below 0.3 ng/ml. CD16+ cells were the most abundant immune cell type in CL during the mid and mid-late luteal phases and were 3-fold increased 3 to 4 days after serum P4 decreased to baseline levels. CD3epsilon+ cells tended to increase 3 to 4 days after P4 decline. To determine whether immune cells were upregulated by the loss of luteotropic (LH) support or through loss of LH-dependent steroid milieu, monkeys were assigned to 4 groups: control (no treatment), the GnRH antagonist Antide, Antide plus synthetic progestin (R5020), or Antide plus the estrogen receptor agonists diarylpropionitrile (DPN)/propyl-pyrazole-triol (PPT) during the mid-late luteal phase. Antide treatment increased the numbers of CD11b+ and CD14+ cells, whereas progestin, but not estrogen, replacement suppressed the numbers of CD11b+, CD14+, and CD16+ cells. Neither Antide nor steroid replacement altered numbers of CD3epsilon+ cells. These data suggest that increased numbers of innate immune cells in primate CL after P4 synthesis declines play a role in onset of structural regression of primate CL.

Keywords: corpus luteum, luteal regression, macrophage, natural killer cell, neutrophil, primate

INTRODUCTION

In nonfertile cycles, luteal regression in Old World monkeys (e.g., macaque species) and humans involves declining sensitivity to luteinizing hormone (LH) pulses, resulting in loss of progesterone (P4) secretion and onset of menses [1]. The events leading to luteal insensitivity to LH and subsequent functional and structural regression near the end of the menstrual cycle are poorly understood in primates. However, luteolysis in some species appears to be mediated, at least in part, by cells of the immune system [2]. Immune processes are conventionally considered to follow two main pathways: innate and adaptive responses [3]. Innate immune processes occur very rapidly and are associated with release of factors such as chemokines and cytokines in response to infection by microbes. Adaptive processes are slower and involve maturation of dendritic cells into antigen-presenting cells in response to inflammatory processes initiated by the innate response and production of specific antibodies to target specific pathogens [3]. Monocytes/macrophages, natural killer (NK) cells, and neutrophils are associated with innate immunity, whereas lymphatic cells (T- and B-lymphocytes) are mostly involved with adaptive immunity, although cellular responses between the two pathways are highly coordinated [3] and not necessarily distinct [4].

Several studies using domestic animal species support a role for immune cells in regulating the functional lifespan of the corpus luteum (CL) [2]. During luteal regression, macrophages, monocytes, neutrophils, and T-lymphocytes increase in number in ruminant CL [5]. Considerable interest was placed on T-lymphocyte population, with three distinct subtypes present in bovine CL that appear to modulate inflammatory processes during luteal regression [5]. In rodent CL, an increase in numbers of luteal macrophages and T-lymphocytes is associated with functional regression, whereas only T-lymphocytes are still elevated at the time of structural regression [6]. There are also reports that the numbers of neutrophils, macrophages (plus their precursor monocytes), and T-lymphocytes increase in the CL of women during luteal regression [710], but it is unclear whether changes occur during functional or structural luteolysis.

Elucidating the processes that regulate accumulation and activation of immune cells within reproductive tissues is an area of active investigation. Local factors such as prostaglandins (e.g., PGE2, PGF2α) have immunomodulatory properties [11], and PGF2α-induced luteal regression is associated with an increase in luteal cytokine production in ruminants [12]. Also, the vital steroid hormone P4, produced by the CL, is generally considered immunosuppressive through direct actions on immune cells [13]. For example, P4 increases the number of a subset of regulatory T-lymphocytes (TReg) within the spleen, lymph nodes, and peripheral blood of pregnant mice [14]; TReg cells suppress local inflammatory cytokines, and this process appears critical to maintaining maternal immune tolerance to the fetus during pregnancy [15]. Mice which lack the gene (Pgr knockout [PRKO]) for the nuclear P4 receptor and, thus, lack both expression of both the PR-A and PR-B receptor isoforms, have increased responses to thymus-dependent antigens, including increased antibody production and increased interferon γ production from isolated T-lymphocytes [16]. However further experiments demonstrated that most of the effects of P4 on bovine immune cells are mediated through the membrane progestin receptor PGRMC1 [17]. Thus, the mechanism of P4 modulation of lymphocyte function appears to vary by species and cell type. Nevertheless, these data support the concept that P4 directly suppresses the activity of T-lymphocytes and inflammatory responses through PR-signaling pathways.

Primate CL in the menstrual cycle also produces estrogens (e.g., estradiol [E2]) in response to LH stimulation with a pattern similar to that of P4 [18]. Effects of E2 on immune cells and inflammation are complex and vary by tissue and disease state [19]. In studies of women receiving hormone replacement therapy with E2 and P4, effects on immune system mediators are reported, but there are limited investigations of women receiving only E2 [19]. Peripheral blood mononuclear cells (PBMCs) express both isoforms of E2 receptor (ERs), ERα (ESR1) and ERβ (ESR2) [20]. PBMC preparations isolated from rats demonstrate that PBMCs are responsive to selective agonists for ESR1/2 [21]. Thus, it is possible that E2, as well as P4, could directly affect PBMC function within luteal tissue.

Our recent microarray studies identified changes in mRNA expression in rhesus macaque CL for immune regulatory components such as proinflammatory chemokines and cytokines, immune cell-associated genes, and gene signaling pathways associated with immune function during the luteal lifespan in the menstrual cycle [22]. For example, gene products associated with cytokine activity were significantly increased in CL collected during luteal regression compared to those from fully functional CL at mid luteal phase [23]. Moreover, microarray analyses of macaque CL collected during gonadotropin-releasing hormone (GnRH) antagonist treatment, which pharmacologically reduces LH secretion and induces premature luteal regression, revealed significant over-representation of gene products associated with several immune pathways including immune system development and leukocyte differentiation [24]. Collectively, these findings suggest that activation of immune pathways within the primate CL is intimately related with onset and progression through luteal regression and may be mediated by loss of luteotropic (LH) support or an LH-dependent local P4 milieu.

Presently it is unknown how prevalent innate or adaptive immune cell populations are in primate CL and whether the total numbers of each cell type change at well-defined stages of the luteal phase in normal menstrual cycles. It is also not clear if luteal immune cell populations are sensitive to the hormonal milieu (i.e., LH or steroids). Given the presence of mRNA encoding many proinflammatory cytokines at the time of regression in macaque CL [22], it is hypothesized that the numbers of many immune cell types and their activity increase within the CL and participate in luteolysis. Although similarities between ovarian processes are observed between model species [25], important species differences are known to exist in regulation and function of immune processes [26]. Thus, the objectives of the current study were to 1) quantify the numbers of several proinflammatory immune cell types present within macaque CL collected throughout the luteal phase of the natural menstrual cycle and to 2) use the model of GnRH antagonist-induced luteolysis to determine whether LH and ovarian steroids regulate the presence of immune cell types within the regressing CL.

MATERIALS AND METHODS

All procedures were performed at the Oregon National Primate Research Center (ONPRC) with approval from the Oregon Health & Science University (OHSU)/ONPRC Institutional Animal Care and Use Committee (IACUC), in compliance with American Society of Primatologists (ASP) Principles for the Ethical Treatment of Nonhuman Primates and the Animal Welfare Act (AWA; 1985) of the United States of America. A cohort of adult female rhesus macaques (n = 25) with a history of normal menstrual cycles were maintained for this study. Hormonal status of each female was monitored for detection of ovulation as previously described [27]; the first day serum E2 concentration declined at midcycle to below 100 pg/ml with a coincident rise in serum P4 was denoted as the first day of the luteal phase, in accordance with previous studies demonstrating that the LH surge occurs on the day before E2 levels decline [28]. Monkeys were under the direct care of the ONPRC Department of Comparative Medicine; all protocols requiring sterile aseptic surgical procedures were performed by trained nonhuman primate surgical veterinarians and technicians in the Department of Comparative Medicine Surgical Services Unit.

CL Collection During the Natural Menstrual Cycle

Females were randomly assigned to undergo lutectomy at various stages of luteal phase during natural menstrual cycles. Individual CL were collected from anesthetized macaques as previously described [29] during the early (Days 3–5 post-LH surge; n = 3 CL), mid (Days 6–8; n = 5), mid-late (Days 10–12 n = 7), and late (Days 15–18; n = 7) luteal phases.

CL Collection Following Induced Luteal Regression

Beginning on Day 9 of the luteal phase (mid-late), macaques (n = 14) were randomly assigned to 4 treatment groups: control (no treatment, n = 4); treatment with the GnRH antagonist Antide to induce early onset of luteal regression, as previously reported (3 mg/kg/day; n = 4; The Salk Institute, La Jolla, CA) [24]; treatment with Antide plus progestin replacement with the synthetic progestin R5020 (2.5 mg/day; n = 3; Perkin-Elmer Inc.); or treatment with Antide plus estrogen replacement with two specific estrogen receptor (ER) agonists, ER1 propyl-pyrazole-triol (PPT) and ER2 diarylpropionitrile (DPN; both 0.15 mg/kg/day, n = 3; Tocris Bioscience) [30]. CL was collected from anesthetized females on Day 12 of the luteal phase, after 3 days of treatment.

Quantification of Immune Cell Populations by Flow Cytometric Analyses

Each CL was weighed and enzymatically dispersed as previously reported [31]. Cells, except for any remaining red blood cells, were then counted using a hemocytometer and assessed for viability by Trypan blue dye exclusion test (Sigma-Aldrich). Equal aliquots of dispersed cells (225 416 ± 22 647 cells/aliquot) from each CL were incubated with fluorescently labeled antibodies (BD Biosciences, Inc.) specific for macaque immune cell surface proteins (1 aliquot/antibody) according to the manufacture's protocol (Supplemental Table S1A; all Supplemental Data are available online at www.biolreprod.org). All antibodies were previously validated for identification of rhesus macaque leukocytes (BD Biosciences) [32, 33]. In addition, each antibody was validated using PBMCs (100 000 cells/aliquot) isolated from potassium/EDTA-treated blood collected from rhesus females as part of this study. Numbers of antibody-labeled cells within a total of 10 000 cells from each aliquot of dispersed cell preparations were assessed using an LSR II model flow cytometer (BD Bioscience) in the ONPRC Flow Cytometry Core. All data were analyzed using FCS Express version 3 software (De Novo Software). A nonimmune, isotype-matched antibody was used as a negative control to define the parameters for quantifying positive cells within each sample (Supplemental Table S1B). Results are reported as the number of marker-positive (+) cells/10 000 cells analyzed.

Statistics

The number of positive cells/10 000 cells recorded for each immune cell type, as well as CL wet weight, total numbers of cells recovered/CL, viability of recovered cells, and total viable cells/CL collected at defined stages of the natural luteal phase of menstrual cycles and after Antide treatment and/or steroid replacement, were analyzed by one-way ANOVA (using generalized liner model [GLM] procedure of SAS version 9.3 software; SAS Institute Inc.). Multiple comparison tests were performed to interrogate differences between CL collected at different stages of the luteal phase, using least square difference (LSD; SAS), which controlled for type I error rate. Serum E2 and P4 levels were analyzed by either one-way ANOVA (individual CL luteal phase) or repeated measures ANOVA (Antide-treated samples) when appropriate (SAS).

RESULTS

Experiment 1: CL of the Menstrual Cycle

Initially, CL collection was based on previously defined stages of luteal development, function and regression (post-LH surge) in female macaques [22]. However, initial flow cytometric analyses discovered wide variation in immune cell numbers in CL collected during the late luteal phase, corresponding to Days 15 to 18 post-LH surge. Further analyses revealed lower numbers of each cell type in CL collected at late luteal phase when serum P4 concentrations were at baseline (0.3 ng/ml) for up to 2 days (functionally regressed; before onset of menses), whereas increased numbers were observed in most CL collected 3 to 4 days after P4 declined (near onset of structural regression, late stage; 1.2 ± 0.4 days post-onset of menses [Day 0]) (Supplemental Fig. S1). Therefore, CL collected during the late luteal phase were separated into these two classifications based on luteal function: early functional regressed stage (P4 < 0.03 ng/ml for 2 days; n = 2) and late stage CL (P4 < 0.03 ng/ml for 3–4 days; n = 5). Subsequent statistical analyses focused on changes in the immune cell populations in the late stage CL compared to those from earlier stages of the luteal phase.

Serum P4 levels were elevated on the day of CL collection at early through mid-late luteal phase but were low in early functional regressed and late stage CL (P < 0.004) (Fig. 1A). Luteal weight of early stage CL was low and increased to a maximum in CL collected at mid and mid-late luteal phases (P < 0.03) (Fig. 1B), corresponding to the interval of peak P4 production. Weight of early functional regressed CL was variable, whereas that of late stage CL was significantly less than CL collected at mid and mid-late luteal phase. Viability of cells recovered did not vary by stage of CL (P > 0.15; overall mean ± SEM 94.4 ± 1.6% viability) (Fig. 1C). Furthermore, total numbers of cells recovered from enzymatic dispersal of CL did not vary significantly by luteal stage (P > 0.9; mean ± SEM 4.1 ± 0.8 million cells/CL) (Fig. 1C). Thus, the total number of viable cells dispersed from CL did not differ between stages of the luteal phase (P > 0.08; mean ± SEM 3.8 ± 0.7 million cells/CL collected; data not shown).

FIG. 1
A) Serum P4 concentrations of female macaques (mean ± SEM, n = 3–7/group; except for those in early regression, which are represented as individual values indicated by gray and black dots, n = 2) on the day of CL collection by stage of ...

Flow cytometry analyses of dispersed cells from the macaque CL detected cell surface markers corresponding to neutrophils/ monocytes/macrophages (CD11b+), monocytes/macrophages (CD14+), and NK cells (CD16+) (Supplemental Table S1). Both CD11b+ and CD14+ cells (Fig. 2) are present at low levels in macaque CL during the developing (early) and functional (mid) luteal phases as well as at the mid-late luteal phase (near the onset of functional regression). Numbers of CD11b+ and CD14+ cells remained low but detectable in CL collected at early regression (Supplemental Fig. S1, A and B). However, CD11b+ and CD14+ cells were 7.5- and 6.2-fold increased, respectively, in dispersed luteal preparations collected during late regression (P < 0.0001) (Fig. 2, A and B). The number of CD16+ cells were 2.7-fold increased in dispersed cell preparations between early and mid-luteal phase (P < 0.03) (Fig. 3A), and were 1.8-fold further increased in late stage versus that in mid-late stage CL (P < 0.05) (Fig. 3A). CD16+ cells were the most abundant immune cell type in CL from early through mid-late luteal phase, but by late luteal stage, the numbers of CD11b+, CD14+, and CD16+ cells in CL were similar.

FIG. 2
Quantification of cells positive for the cell surface markers CDllb (A) and CD14 (B) in dispersed cell preparations of macaque CL collected at discrete stages of normal luteal phase (mean ± SEM, n = 3–7/group [see Materials and Methods ...
FIG. 3
Quantification of numbers of CD16+ (A) and CD3ε+ (B) cells in dispersed cell preparations of CL collected at discrete stages of luteal phase (mean ± SEM, n = 3–7/group [see Materials and Methods for details]). Different letters ...

Low numbers of CD3ε+ cells (T-lymphocytes) were detected in dispersed cells from CL collected at all stages of luteal phase and were typically fewer in number than CD11b+, CD14+, and CD16+ cells. Although overall changes in numbers of CD3ε+ cells analyzed by one-way ANOVA from all CL collected throughout the luteal phase were not significant (P = 0.07) (Fig. 3B), the numbers of CD3ε+ cells did increase in CL collected at late compared to those collected at mid-late luteal phase (LSD mean comparison test; P = 0.05). Numbers of CD20+ cells (B-lymphocytes) in macaque CL were extremely low when present (<30 positive cells/10 000 in 6 of 23 CL). However, CD20+ cells were reliably detected in PBMC preparations (data not shown).

Experiment 2: GnRH Antagonist-Induced Luteal Regression

Administration of the GnRH antagonist Antide at mid-luteal phase of the menstrual cycle significantly reduced serum P4 levels by 24 h (effect of Antide; P < 0.001) (Fig. 4A) and E2 levels by 48 h (P < 0.001, data not shown). Steroid levels remained low throughout the remainder of the treatment interval until CL collection at 72 h. Concomitant treatment with progestin (R5020) or estrogen agonists (DPN/PPT; ERα/ERβ agonists) did not increase serum levels of endogenous P4 or E2 compared to that of Antide alone (Antide vs R5020 or DPN/PPT, P > 0.05; it is important to note that the radioimmunoassays used in this study for measuring both P4 and E2 used antibodies which do not cross-react with R5020 or DPN/PPT, respectively). Previous studies in rhesus females using the same dose of R5020 reported serum concentrations of progestin at between 6 and 7 ng/ml [34], similar to physiologic concentrations of P4 in functional CL. Treatment with Antide caused premature menstruation in all females at the time of CL collection (Day 12 post-LH surge). In contrast, none of the females treated with both Antide and R5020 displayed menses until at least 5 days after luteal collection. Menses occurred on the day of CL collection or one day later in the Antide plus DPN/PPT-treated monkeys. Three days of Antide exposure reduced CL wet weight compared to that of untreated control CL (P < 0.02) (Fig. 4B), and CL weight was unaffected by coadministration of R5020 or DPN/PPT relative to that with Antide alone. The total number of cells recovered by enzymatic dispersal of CL was unaffected by treatments (P > 0.3; mean ± SEM 3.2 ± 0.4 million cells/CL) (Fig. 4C). Also, percentage of viability of recovered cells was unaffected by treatments (P > 0.17; mean ± SEM 92 ± 1%) (Fig. 4C). Thus, the number of viable cells in dispersed cell preparations were not affected by any treatment (3.0 ± 0.4 million viable cells/CL; data not shown; P > 0.3).

FIG. 4
A) Changes in serum P4 levels before (Day 9) and during 3 days of treatment with Antide alone or with the synthetic progestin R5020 (A+R5020) or E2 receptor agonists DPN/PPT (A+DPN/PPT) during the mid-late luteal phase (mean ± SEM; n = 3–4/group). ...

Three days of Antide treatment markedly increased the numbers of CD11b+ and CD14+ cells (10.7- and 8.3-fold, respectively) in dispersed cell preparations of CL compared to that in cells from untreated controls (P < 0.0004 and 0.005, respectively) (Fig. 5, A and B). Concurrent treatment with R5020 prevented Antide-induced increase in CD11b+ and CD14+ cells (P < 0.002 and 0.008, respectively; Antide vs. Antide plus R5020) (Fig. 5, A and B). However, the increase in CD11b+ and CD14+ cells caused by Antide treatment was not affected by coadministration of E2 agonists (P > 0.5) (Fig. 5, A and B). Antide alone did not alter the numbers of CD16+ cells (Fig. 5C), but concurrent treatment with R5020 suppressed their numbers in CL (Antide vs. Antide plus R5020; P < 0.03) (Fig. 5C). However, addition of E2 agonists did not significantly alter the numbers of CD16+ cells compared to Antide treatment alone. The numbers of CD3ε+ cells in dispersed cell preparations were not significantly influenced by Antide alone (P > 0.3), Antide and R5020 (P > 0.9), or Antide and DPN/PPT (P > 0.3) (Fig. 5D).

FIG. 5
Quantification of CD11b+ ([A] monocytes, macrophages, and neutrophils), CD14+ ([B] monocytes or macrophages), CD16+ ([C] NK cells), and CD3ε+ ([D] T lymphocytes) cells in dispersed cell preparations of macaque CL collected 3 days after Antide ...

DISCUSSION

Binding of the CD11b antibody to a subpopulation of dispersed cells from the macaque CL strongly suggests that macrophages and/or neutrophils are present in primate luteal tissue. The cell surface antigen CD11b, also known as Mac-1 or integrin, alpha M (complement component 3 receptor 3 subunit; ITGAM, National Center for Biotechnology Information (NCBI) gene ID: 3684) is part of an alpha-M/beta 2 integrin involved in immune cell migration and is expressed primarily by macrophages/neutrophils [35]. The low numbers of neutrophils/macrophages in dispersed cell preparations from macaque CL collected during the functional (early to mid-late) luteal phase versus the large numbers present at the late luteal phase, at onset of structural regression, is consistent with previous reports on CL of women [36, 37], and domestic animals [5]. Macrophages and neutrophils secrete many similar cytokines and express several similar cell surface receptors and, thus, have overlapping and complementary local actions [35]. Macrophages are associated with tissue remodeling and are reported to destroy neoplastic cells in tumors (termed tumor-associated macrophages [TAMs]) [38]. Furthermore, these TAMs secrete proteases which can degrade extracellular matrix proteins and liberate fragments of fibronectin/fibrinogen, which serve as chemoattractants to other immune cell types [39]. Luteal macrophages may have similar functions. Neutrophils are recruited to tissues by cytokine gradients produced by local macrophages in response to injury or infection, where these cells secrete proinflammatory chemokines and cytokines to modulate the local immune responses [40], which may be involved in progression of luteolytic processes.

Because CD11b is expressed on both macrophages and neutrophils, an antibody to the CD14 cell surface protein (NCBI gene ID: 697482) was used to confirm the presence of macrophages in the cells populating the macaque CL. This cell surface protein has higher expression on macrophages than on neutrophils and functions to enable these cells to coordinate local immune responses [41]. The proportion of CD14+ cells can be compared to CD11b+ cells to estimate the local population of neutrophils within cell preparations. Patterns for numbers of CD11b+ and CD14+ cells during stages of the luteal phase were identical. In cell preparations from the early luteal phase, the number of CD14+ cells (macrophages) is 90% of that for CD11b+ cells (total neutrophils/macrophages), whereas the number of CD14+ cells is 65% of CD11b+ cells in CL during late regression (when P4 levels were at baseline for 3–4 days). This suggests most neutrophils migrate into the CL in late luteal phase, possibly following gradients of chemokines produced by the increased numbers of macrophages.

The presence of NK cells within monkey CL was detected by antibody binding to the cell surface receptor CD16 (FCGR3; NCBI cene ID: 720006); they were the most numerous immune cell type within dispersed cell preparations of macaque CL during the functional luteal phase and remained elevated during late luteal regression. Although some macrophages coexpress CD11b and CD16, the number of CD11b+ cells are much lower than the CD16+ cells in CL during the functional luteal phase (i.e., early through mid-late stages), indicating a distinct population of NK cells in macaque CL. Our data are consistent with those of one report [10] of immunostaining for NK cells within the human CL and provide evidence of their dynamics during the primate luteal lifespan. Primate NK cells are divided into two subtypes: immature (5% of total population) and mature (95% of population) NK cells [42, 43]. The immature subtype secretes more cytokines than mature NK cells, whereas mature NK cells function mainly to lyse target cells through a major histocompatibility complex (MHC)-independent mechanism (as reviewed by Caligiuri [43]). One function of neutrophils is to induce NK cell maturation [40]. Most research to date on NK cell function in the reproductive tract focuses on their role during embryo implantation and placentation within the uterus [44]. It is important to mention that most primate uterine NK cells are CD56bright, and increased numbers of CD56dim NK cells in the uterus are associated with reproductive failure [45], notably, a subpopulation of primate NK cells is CD16+ CD56dim [46]. This could explain why some previous investigations failed to identify NK cells in primate luteal tissue (e.g., in the human ovary) [47]. The function of NK cells has yet to be studied in the non-neoplastic ovary, but there are some reports on the use of peripheral cytotoxic NK cells as therapy for ovarian cancer [48, 49]. Because NK cells appear to promote placentation and uterine vascular remodeling [44], they may have a similar role in promoting vessel growth, maturation and stability during formation (early) and function (mid- to mid-late) of the CL, before assuming degenerative roles during luteal regression. NK cells may be considered the innate counterparts of cytotoxic T cells [4] and may switch from tropic to lytic roles during the lifespan of primate CL much as proposed for T cells in the CL of domestic animals [2, 50]. The dual functions of both NK and T cells contribute to the overlap in cells participating in innate and adaptive immune responses [4], and thus further investigation into cytokine/chemokine production by ovarian NK cells are warranted.

Unexpectedly, immune cells conventionally associated with adaptive immune responses, including T as well as B cells, only sparsely populated the macaque CL. Because CD20+ cells were largely undetectable in dispersed CL preparations collected throughout the luteal phase, the small number of B-lymphocytes likely reflects contamination from circulating blood cells. Our findings support immunohistological evaluations [47], which also report lack of CD20 immunostaining in CL of women. The presence of T-lymphocytes in macaque CL was noted by detection of cells binding antibody to the cell surface receptor CD3ε (CD3E; NCBI gene ID: 699467), part of the T-cell receptor complex that is present on all T-cell populations. The T-cell population was fewer in number than macrophages, neutrophils, and NK cells, and the numbers of T-lymphocytes only modestly increased in CL isolated during the late luteal phase at onset of menses (Fig. 3B). Lower numbers of CD3ε+ cells were also observed in the CL of women by immunohistological methods, with an increase in abundance in regressing CL near onset of menses [47]. Our findings contrast with several reports using domestic animal models wherein large increases in CD4+ and CD8+ T-lymphocytes occurred in CL at the onset of regression [5, 50]. CD3ε antibody was chosen as a marker of T-lymphocytes in the current study because the CD3ε receptor is expressed selectively by all T-lymphocytes, unlike CD8 which is typically coexpressed with CD16 in primate NK cells [51]. Studies in bovine CL focused on a particular subtype of T-cell, CD8+γδ T-cells. This subtype increases during luteolysis in ruminants, whereas other T-cell subtypes, including TReg, decrease [50]. Changes in T-cell subtypes may not have been detected in macaque luteal tissue in the current flow cytometry analyses due to use of a pan T-lymphocyte marker. Future analyses could reveal more remarkable dynamics and possible roles for T-lymphocytes subtypes in primate CL that are not captured by changes in total T cells.

In the current study, premature luteal regression, induced by treatment with the GnRH-antagonist Antide, resulted in changes in immune cell numbers in dispersed CL preparations that generally equated with those observed during natural luteolysis. Both CD11b+ and CD14+ cells (and to a lesser extent CD3ε+) increased to levels observed in CL during the late luteal phase of the natural menstrual cycle. The numbers of CD16+ cells may not have increased due to their higher level in the functional CL, as well as the structurally regressing CL. Although Antide treatment resulted in loss of both LH and LH-induced steroid hormones, data strongly suggest that the numbers of neutrophils, macrophages, and NK cells within macaque luteal tissue are regulated by P4 but not by E2. Concurrent treatment with the progestin R5020 suppressed numbers of macrophages, neutrophils, and NK cells. Thus, high levels of P4 from/within the functional CL may limit the numbers of these immune cells, whereas the loss of P4 in the regressing CL permits their numbers to increase. The mechanism(s) of P4 action awaits investigation; whether these effects are mediated by progestin receptor(s) in luteal cells and/or directly on immune cells is unknown. Human peripheral blood macrophages express the nuclear PGR [52], and P4 decreases the inflammatory response from peripheral primary monocytes [53]. Apoptosis of peripheral blood NK cells can be induced by P4 in a dose-dependent manner; this effect was only detected in NK cells coexpressing PGR [54]. In contrast, CD56bright NK cells in the uterus reportedly lack PGR [55], but it is unknown whether the CD16+ NK cell population in primate CL possess PGR or other progestin receptors. Although bovine T-lymphocytes express different types of membrane progestin receptors [13], there were no effects of either Antide-induced LH withdrawal or progestin replacement on the total number of CD3ε+ T-lymphocytes in macaque cell preparations in the current study. Because reports suggest a direct role for P4 through progestin receptors [16, 17], and species-specific differences in regulation and function of immune cell types [26], further investigation of steroid regulation of immune cells in primate CL is warranted.

The transition from early to late regressive events is associated with an increase in the percentage of most immune cell types in rhesus CL. Early regression, although not investigated in depth here, appears to correspond to the time of functional regression in which steroidogenic activities of the CL cease [23, 56]; steroidogenic luteal cells appear to shrink in size [57] as cholesterol stores are actively shuttled out of the cells [58]. This is distinct from onset of structural regression; the late luteal phase of the menstrual cycle, when P4 levels are at baseline for at least 3 days, appears to correspond to the time of onset of structural regression. Structural luteal regression is a time of major tissue remodeling and destruction, based on immunohistochemical analyses of increased collagen fiber deposition [59] and decreased numbers of vascular endothelial cells [60]. Collectively, these result in changes in gene products for proteases, extracellular matrix components, and angiogenic/angiolytic factors in the CL [23, 61] allowing for the formation of the remnant structure, the corpus albicans. Morphological studies of marmoset monkey ovaries containing luteal tissue suggest that this process can last into the late follicular phase of the subsequent menstrual cycle, indicating a lengthy duration of luteal structural regression in primate species compared to others [62]. This lengthy delay suggests that multiple processes might occur in luteal tissue between a loss of sensitivity to LH (manifested by lower P4 secretion) and increases in luteal immune cell numbers.

The number of macrophages/monocytes and neutrophils (CD11b+ cells) present in dispersed CL collected at the late stage comprises ~18% of the total population analyzed. These data are consistent with previous flow cytometry studies of dispersed luteal tissue from women. Castro et al. [9] reported that the total leukocyte population within the luteal preparations was between 20% and 50% of all cells analyzed, but the percentage of CD14+ macrophages did not differ in CL staged among early, mid-late, and late phases (10–14 days following ovulation) of natural menstrual cycles [9]; however, serum P4 levels were not reported for these women. Whether this represents invasion of luteal tissue by immune cells or an increase in proportion of immune cells as a function of total cell population is not known. Similar percentages of viability of dispersed CL are reported for women (>90% [9]) and for macaques by this analysis. It is possible that degenerating/apoptotic cells (either luteal, endothelial, or other types) were lost during enzymatic dispersal of the luteal tissue or structural degeneration at time of luteolysis, leading to an enrichment of immune cells at later stages of the luteal phase. Increased numbers of immune cells, coupled with loss of nonimmune cell types would result in constant numbers of total cells in the CL, independent of cycle stage, as observed in this study. Recent immunohistochemical analyses of regressing CL from women at menses found putative macrophages to be the predominant cell type within cross-sections of luteal tissue, confined to strict regions adjacent to steroidogenic (luteal) cells [63]. It is reported in rhesus monkeys that the large-to-small cell ratio in CL decreases in latter stages of the luteal phase, but some of these small cells retain the ability to secrete P4 if stimulated by LH [57]. Given these data, it is unlikely that the large increase in immune cell populations found in late regression is an artifact. Further investigations into the processes activated during this transitional period are needed.

It is important to recognize, however, there are low numbers of macrophages present in macaque luteal tissue immediately prior to and at the time of functional regression (Fig. 2 and Supplemental Fig. S1). Although low in number, these immune cells may be secreting cytokines to facilitate luteal remodeling during structural regression and secreting chemoattractants to recruit greater numbers of monocytes/macrophages, as well as neutrophils and NK cells and, to some extent, T-lymphocytes to luteal tissue to promote further regressive events. One major product of proinflammatory macrophages, which also has chemoattractant activity, is monocyte chemoattractant protein 1 (MCP1 [also known as CCL2]) [64]; Affymetrix rhesus macaque microarray studies reveal CCL2 mRNA is present at low levels throughout the macaque luteal phase, increasing 2-fold in very late CL staged by days post-LH surge (GEO dataset Series GSE10367; [22]). Furthermore, studies in women report increased CCL2 protein within CL collected at menses with concurrent increases in cells staining positive for the macrophage marker CD68 [63]. Intriguingly, CCL2 is expressed by granulosa- and theca-lutein cells, suggesting that steroidogenic cells of the CL are producing chemotactic signals, resulting in increased numbers of luteal immune cells during luteal regression [63]. Our microarray studies of LH/steroid ablation and progestin replacement (dataset series GSE12281; GEO) [24] revealed a large number of gene products associated with immune system processes that are regulated in primate CL directly by LH or indirectly through LH-stimulated P4 production. Of note, mRNA for chemokine (C-C motif) receptor 1 (CCR1) increases 13.6-fold in CL collected from rhesus females following exposure to Antide, as well as mRNA for the CCR1 ligand chemokine (C-C motif) ligand 3 (CCL3; 10.5-fold increase, data not shown). CCR1 protein is expressed by monocytes/macrophages, neutrophils, and T-cells [65], and CCL3/CCR1 signaling is reported to induce macrophage migration/infiltration [66]. Further studies will investigate the functional potential of NK cells, neutrophils, and macrophages during the functional and late (structurally regressing) stages of the luteal phase.

In summary, these data demonstrate a significant increase in several types of immune cells (i.e., macrophages, neutrophils, and NK cells) in primate CL during the late luteal phase, corresponding to the onset of structural luteolysis. Data presented here suggest, for the first time, that NK cells have a major role in promoting the structure and function of primate CL during mid and mid-late luteal phases. We report that NK cells are the most prevalent immune cell type during the functional luteal phase. Following a decline in P4 levels to baseline for at least 3 days, there is a remarkable increase in neutrophils, monocytes/macrophages, NK cells, and to some extent, T-lymphocytes, suggesting that activation of multiple signaling pathways within primate CL facilitates this event. The increase in CD11b+/CD14+ macrophages/neutrophils in luteal tissue after removal of gonadotropic support is dependent on the loss of LH-dependent P4 synthesis. Replacement of progestin following Antide exposure suppressed the numbers of luteal CD16+ NK cells, possibly through the immune-suppressive actions of P4 unrelated to LH. The presence of CD3ε+ T-lymphocytes in primate CL is not dependent on either LH or LH-dependent P4 secretion, and CD3ε+ T-lymphocytes are the least abundant cell type in luteal tissue quantified during the functional luteal phase and during regressive events. The results are consistent with the concept that signaling processes activated during early functional regression, marked by a decline in P4 secretion and local action, promote processes that induce changes in numbers of luteal immune cell populations during the latter stages of functional regression. Further experiments are needed into the signaling cascades activated during this transitional period in primate CL.

ACKNOWLEDGMENT

The authors would like to recognize assistance by Jonah Sacha, PhD, and Ilhem Messaoudi, PhD, and associates in the ONPRC Division of Pathobiology and Immunology for assistance in selecting the nonhuman primate antibodies used in this study. The authors are grateful to the ONPRC Flow Cytometry Support Core and Endocrine Technology Support Core Lab for assistance with these studies. In addition, we thank the OHSU Flow Cytometry Shared Resource for providing software and guidance with data analyses. These studies would not be possible without the outstanding animal care and support provided by the ONPRC Department of Comparative Medicine and Surgical Support Unit.

Footnotes

1Supported by grants R01HD020869 to R.L.S. and P51OD011092 to the Oregon National Primate Research Center. These data were presented in part at the 45th Annual Meeting of the Society for the Study of Reproduction, August 12–15, 2012, State College, Pennsylvania, and at the 46th Annual Meeting of the Society for the Study of Reproduction, July 22–26, 2013, Montréal, Québec, Canada.

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