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Islet-infiltrating lymphocytes of individual male and female non-obese diabetic (NOD) mice were examined with the purpose of determining the differences that lead to a predominance of diabetes in female versus males NOD mice. When normalized for the amount of islet lymphocytes recovered, the infiltrating lymphocytes of female NOD mice were indistinguishable from those of male NOD mice. The only observed difference was that islet inflammation progressed at an increased rate in female compared to male NOD mice. There was no difference in the composition of islet infiltrates in male and female NOD mice. Unexpectedly, the ratio of CD4+:CD8+ T cells was tightly controlled in the islets throughout diabetogenesis. The frequency of IL-4+ CD4+ T cells started high but quickly fell to 3% of the population which was maintained with increasing inflammation. A significant portion of the CD8+ T cells were islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP) specific in both male and female NOD mice and this population was antigen experienced and increased at high levels of islet inflammation. Surprisingly, a large pool of antigen inexperienced naïve T cells was detected in the islets. We conclude the underlying immunological processes in both male and female NOD mice are similar while the rates differ and the presence of naïve T cell in the islets may contribute to epitope spreading.
Type I diabetes (T1D) is caused by the immune destruction of the insulin-producing pancreatic β cells. Based on studies with the non-obese diabetic (NOD) mouse, the primary mediators of β cell destruction are CD4+ and CD8+ T cells 1–3. NOD mice spontaneously develop T1D, with 80% of females and 20% of males becoming overtly diabetic by 20 weeks of age4. The immunological basis for the disparity between the sexes, however, is not well characterized 5,6. Sex hormones influence the time of onset of T1D. Disease incidence is increased in castrated NOD males and administration of testosterone delays the onset of disease in NOD females7–10. In addition, several studies have examined the Th1/Th2 cytokine balance in male and female NOD mice and found that T cells were skewed to produce more Th1 cytokines in young females than in young males, although islet infiltrating cells from both male and female NOD mice can produce diabetes in NOD scid mice 11–13. Presently, the effect of the sex hormones on the immune system remains poorly understood and the balance of lymphocyte subsets in the islets in NOD males versus females over time has not been studied.
Susceptibility to diabetes is genetically linked in both NOD mice and humans to the MHC class II alleles. NOD mice deficient in β2-microglobulin and CD8+ T cells fail to develop diabetes. Thus, both CD4+ and CD8+ T cells are important for development of diabetes in NOD mice 14–25. Given the importance of T cells in T1D, there have been many attempts to understand their role in the progression of β cell autoimmunity 26,27. Unfortunately, these efforts have been hampered by the paucity of T cells that can be recovered from the islets. As a result, many studies have used pooled islets from several NOD mice, pancreatic lymph nodes (PLN), or spleen cells to study the progression and nature of the autoimmune response 12,28–31. While these studies have aided in elucidating the systemic immune response, a critical analysis of the T cell response in the islets from single individuals is still lacking.
Using multi-color flow cytometry we directly analyzed the islet-infiltrating lymphocytes of individual male and female NOD mice, then considered the data both as individual mice and in groups. Islets of female NOD mice were more heavily infiltrated than the islets of age matched males. Surprisingly, when considered as individuals and matched by the level of lymphocyte infiltration instead of age, the composition of islet infiltrates of male NOD mice resembles that of females. The number of both IL-4+ CD4+ T cells and Treg increased over time in the islets. In spite of this increase, the percentage of IL-4+ CD4+ T cells decreased. Interestingly in the midst of these changes, the ratio of CD4+:CD8+ T cells in the islets remained constant. Male NOD mice had antigen experienced IGRP reactive CD8+ T cells in their islets. These data indicate that male and female NOD mice progress towards diabetes with the same balance of lymphocytes, but at very different rates. A surprising finding of this study was the presence of significant levels of antigen inexperienced, apparently naïve, T cells in the islets of NOD mice.
NOD/ShiLtJ mice and C.129-Il4tml Lky/J mice were purchased from Jackson Laboratories32. In our facility, female NOD mice become diabetic at a median age of 16 weeks, with 75% diabetic by 20 weeks of age indistinguishable from NOD/ShiLtJ mice at Jackson Labs(see Supplemental Fig. 1). In order to examine T cells with a Th2 phenotype, NOD IL-4 reporter mice (NOD.Cg-Il4tml Lky/Fre) were created by backcrossing the reporter gene from C.129-Il4tml Lky/J mice onto the NOD background using speed congenics 32,33. These NOD mice express eGFP when IL-4 mRNA is produced. Forty-three SNPs (Supplemental data Table 1) were used to distinguish between the BALB/c and NOD genomes. The IL-4 gene, located on chromosome 11 at base pair position 53 million, was flanked by SNPs at positions 33 million and 77 million; both were homozygous for NOD DNA. By backcross (BC)4 (N5), 41 of the 42 SNPs were homozygous for NOD markers (98.8% of the SNPs) and female mice in the N4 or BC3 generation became diabetic. The mice were backcrossed 3 more times without SNP selection to BC6 to assure homogeneity of the NOD genetic background. To select newly diabetic mice, blood sugar was monitored weekly using a FreeStyle Blood Glucose Meter and mice were considered diabetic after 2 consecutive blood glucose readings of over 250 mg/dL. Only mice with a blood sugar <150 mg/dL were used in this study, unless specifically designated as a diabetic mouse.
Pancreata were isolated as previously described 34. Briefly, each pancreas was perfused with a 2 mg/ml solution of Collagenase P (Sigma), dissected and incubated at 37°C for 20 minutes. Islets were purified using a Ficoll PM 400 (Sigma) gradient, handpicked, counted and then cultured overnight in RPMI 1640 media containing 10% FBS and 4 ng/ml recombinant murine IL-2 (Invitrogen). Infiltrating lymphocytes were collected and filtered through a 40μm nylon filter. All islet-infiltrating cells from every mouse were analyzed by flow cytometry. Because the number of islets recovered is not uniform among mice, the “number of cells per islet” was determined by dividing the total number of cells in the sample by the number of cultured islets; therefore, a mouse that had 100 CD8+ T cells, 400 CD4+ T cells and 300 B cells recovered from 100 islets would be recorded as having 1 CD8+ T cell, 4 CD4+ T cells and 3 B cells per islet. Each sample constitutes all of the islet cells isolated from an individual mouse. An average of 103 islets was isolated per mouse. For further examples of how data was collected and treated, a chart of the raw data presented in Fig. 3 is included (Supplemental data Table 2). The data from each individual mouse was analyzed individually or alternatively combined with the data from mice of like sex and age to examine inter group differences.
Splenocytes and lymphocytes from NOD mice were examined using 9 color flow cytometry. Cells were stained with a cocktail of APC-Cy7-anti-CD3 (BD Biosciences, San Jose, CA), Pacific Orange-anti-CD4 (Invitrogen, Carlsbad, CA), PerCP-anti-CD8 (BD), Pacific Blue-anti-CD44 (Invitrogen), APC-anti-CD25 (eBioscience), PE-Texas Red-anti-CD62 (Invitrogen), PE-Cy7-anti-CD19 (BioLegends, San Diego, CA) and PE-ultra-avidin (Lenco, St. Louis, MO)-NRP-V7-Kd tetramer. Antibody concentrations used were determined by preliminary titrations. To assess FoxP3 expression, cells were fixed, permeablized and stained with PE-anti-FoxP3 antibody (eBioscience). Cells were analyzed on a Dako (Beckman-Coulter) Cyan-ADP(Colorado Springs, CO). “Minus one” controls were performed in each experiment to ensure that the fluorescence measured originated from the correct stain. Staining controls used syngeneic spleen cells.
H2Kd tetramers were prepared as previously described 35. Briefly, H2Kd, modified to contain a biotinylation sequence, and mouse β2 microglobulin were produced in E. coli and refolded with NRP-V7 peptide (KYNKANVFL from GenScript) in vitro, an islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP) mimotope 36. Refolded NRP-V7-H2Kd monomer was purified by HPLC, biotinylated using Biotin Protein Ligase and assembled into tetramers by conjugation with UltraAvidin-R-PE (Leinco). In NOD mice most of the IGRP+ CD8+ T cells are also NRP-V7+. For convenience, NRP-V7 reactive cells are referred to as IGRP-specific.
We examined the number of T cells infiltrating the islets. In both NOD males and females, the number of CD4+, CD8+ and B cells increased with age. In NOD males, there was an ~two-fold increase in the number of infiltrating cells, whereas a five-fold increase of CD4+, CD8+ and B cells was detected in NOD female mice between 6–8 and 12–14 weeks of age (Fig. 1A). This is consistent with previous reports that islets of NOD female mice are more heavily infiltrated than NOD male mice of the same age 5. However, it is of note that the number of infiltrating cells in males also increased with age, albeit more slowly than in females. 25–29 week-old male NOD mice were examined to determine if β cell autoimmunity continued to increase in males and levels of insulitis comparable to those seen in the 12–14 week-old females was achieved, or if insulitis in males was arrested at a certain point and did not progress. We found that 25–29 week-old male NOD mice had levels of islet lymphocytes similar to 12–14 week-old female NOD mice. By 25–29 weeks nearly all female NOD mice became overtly diabetic (Supplemental Fig. 1). We considered diabetic mice separately regardless of age and no diabetic mice were included in the analysis unless explicitly noted.
We determined the composition of infiltrating cells over time in spleen, peripheral and PLN and the islets of NOD mice. Surprisingly, when grouped into 6–8 week and 12–14 week-old, males and females, there was no significant change in the percentage of CD4+, CD8+ or B cells over time in the spleen, peripheral lymph nodes, PLN or islets (Fig. 1B). Thus, while the number of infiltrating cells increased, the overall composition did not change.
When individual NOD mice were examined, regardless of their sex or age, a linear relationship between the number of CD4+ and CD8+ T cells per islet was detected, indicating a strong association between the number of CD4+ and CD8+ T cells that is maintained in the islets during the progression of β cell autoimmunity in both males and females (Fig. 1C) (r2= 0.9735). The number of B cells also increased linearly with CD4+ T cells (r2 of 0.7212); however, the ratio of B cells to CD4+ T cells was less tightly regulated compared to CD8+ T cells (Fig. 1C and D).
To further investigate the ratios of lymphocyte subsets as β cell autoimmunity progressed, we examined diabetic female NOD mice and 25–29 week-old male NOD mice. Diabetes is the consequence of β cell autoimmunity; however, loss of blood glucose homeostasis could alter the control mechanism. Therefore, islets were isolated from female NOD mice within 10 days of a blood glucose level >250 mg/dL. These mice had a CD4+:CD8+ T cell ratio of 2.7+/− 0.52, similar to non-diabetic female NOD mice (Fig 2). We then examined 25–29 week-old non-diabetic male NOD mice and found a statistically equivalent CD4+:CD8+ T cell ratio of 3.5+/− 0.77; again indistinguishable from younger non-diabetic females (Fig 2). Therefore at the onset of diabetes and in very old male NOD mice the number of infiltrating cells had greatly increased but the CD4+:CD8+ T cell and B cell:T cell ratios remained the same.
Th2 cell responses have been suggested to regulate at least some Th1 and Tc1 cell responses 37,38. We examined the expression of IL-4 secreting CD4+ T cells using NOD IL-4 reporter mice 32,39. The percentage of IL-4 producing CD4+ T cells was much higher in the islets of males and young females than in the spleen, peripheral lymph nodes and PLNs (Fig. 3A). The level of IL-4 producing CD4+ T cells in the spleen and periphery was the same in all mice regardless of sex and age. In contrast the percentage of IL-4 producing CD4+ T cells in the islets decreased with age in both males and females. When individual mice were examined, it became obvious that mice with low levels of infiltrates had higher levels of IL-4 producing CD4+ T cells (Fig. 3B & C). The percentage of IL-4 producing CD4+ T cells decreased before the number of CD4+ T cells reached 25 per islet, then maintained a constant level, consisting of ~3% of the CD4+ T cell population. Surprisingly when the number of IL-4 producing CD4+ T cells was directly compared to the total CD4+ T cells per islet, the number of IL-4 producing CD4+ T cells increased linearly with the increase of CD4+ T cell per islet, r2=0.94. The best fit line had a slope of 0.03 indicating an overall composition of 3% IL-4 competent cells in the CD4+ T cell population (Fig. 3D). At very low numbers of infiltrating CD4+ T cells, those cells are highly IL-4 producing. This was suggested because the best fit line does not pass through zero (see Supplemental Fig. 3). Close inspection of the raw data confirms that when very few cells (<50 CD4+ T cells/mouse) were recovered from the islets, they are 34% IL-4 competent. Overall our data demonstrates that the first CD4+ T cells to reach the islets had an increased percentage of IL-4 competent cells and while the IL-4 producing CD4+ T cells increased, they initially did so more slowly than the non-IL-4 producing CD4+ T cells and so were not able to influence the diabetegenic cells effectively.
FoxP3+ Tregs are important in regulating autoimmunity. Strikingly, the frequency of FoxP3+ CD4+ T cells in the spleen, peripheral lymph nodes and PLNs was similar and stable at ~7–12% at all times examined. The highest level of Treg was in the islets where the frequency of Treg increased in NOD males between 6 and 12 weeks of age. The percentage decreased in NOD females, despite an increased number of FoxP3+ CD4+ T cells per islet over this same time (Fig. 4A, B and C). Thus, the drop in frequency in females was due to dilution in a greater number of FoxP3− CD4+ T cells. In individual NOD mice, the percentage of FoxP3+ CD4+ T cells was high in the early stages of β cell autoimmunity, with the exception of a few mice that had very few cells in the islets, but gradually decreased after 50 CD4+ T cells per islet (Fig. 4D). When the analysis was repeated using the CD25hi population as a surrogate marker for Treg, similar results were obtained (Fig. 4C). In 12–14 week-old male NOD mice, 20 percent of the islet-infiltrating CD4+ T cells were CD25hi, compared to only 13–15% were CD25hi in the islets of 25–29 week-old NOD male mice, indicating that Treg also decreased in males but at an older age. This suggests that Treg might be effective in young NOD females and older NOD males.
IGRP is a known target of diabetogenic CD8+ T cells. A striking increase in the number, but not the percentage of IGRP-specific CD8+ T cells was detected in the islets (Fig. 5). The number of IGRP-specific CD8+ T cells in the islets of older NOD females increases 10-fold compared to age matched males (Mann Whitney test p= 0.004) (Fig. 5B). Nevertheless, 25–29 week-old male NOD mice had levels of IGRP-specific CD8+ T cells comparable to the 12–14 week-old females. Also the percentage of CD8+ T cells that were IGRP-specific was similar in NOD males and females (Fig. 5C). In contrast to the phenotype of IGRP-specific CD8+ T cells found in the periphery, nearly all of the IGRP-specific CD8+ T cells in the islets were effector phenotype, CD62Llo and CD44hi (Fig. 5A). In the periphery there was a significant fraction of naïve, CD62Lhi and CD44lo, or memory cells, CD62Lhi and CD44hi, but relatively few IGRP-specific CD8+ T cells with an effector phenotype (Fig. 5D). Thus the IGRP-specific CD8+ T cells in the islets of both male and female NOD mice are antigen experienced. This is consistent with previous research demonstrating islet-infiltrating lymphocytes can transfer diabetes to NOD scid recipients 11.
We examined the relationship of CD8+ T cell number to the number of IGRP-specific CD8+ T cells. Interestingly, when the islets reached a critical level of inflammation (as defined by the number of CD8+ T cells/the number of islets from individual mice), the number of IGRP-specific CD8+ T cells increased faster than the total number of CD8+ T cells infiltrating the islets of NOD mice (Fig. 6A). The change in rate suggests that the total number of T cells increased at a constant rate, but IGRP reactive CD8+ T cells increased more rapidly in the islets. Indeed, this is consistent with expansion in situ the IGRP-specific CD8+ T cells made up a major subset of the effector CD8+ T cells in the young animals (Fig. 6B).
While nearly all of the IGRP-specific CD8+ T cells in the islets were CD44hi and CD62Llo indicating they were antigen experienced and effector cells, a large portion of the CD8+ T cell pool in the islets was CD44lo and CD62Lhi indicating they are not antigen experienced and appear to have a naïve phenotype (Fig. 7A). The percent of CD44lo, CD62Lhi CD8+ T cells increased with age in both male and female NOD mice (Fig. 7B). An equivalent population was also observed in the CD4+ T cell pool; however, a smaller portion of the CD4+ T cell pool had a naïve phenotype in the islets (Fig. 7C). When individual mice were compared, naïve T cells increased with increasing insulitis (Fig. 8).
We re-examined IL-4 competent T cells in the islets and found they were all CD44hi and CD62Llo, thus effector cells (data not shown). FoxP3+ CD4+ T cells were all CD44hi with some CD62Llo cells and some CD62Lhi cells, thus effector and memory cells (data not shown). Thus, the naïve phenotype cells in the islets were unlikely to be anti-islet CD8+ T cells, Th2 cells or Treg cells. This demonstrates an influx of peripheral naïve T cells.
Naïve T cells are not detected until the number of CD4+ T cells reaches 6.4 CD4+ T cells per islet indicating a threshold for inflammation is needed before naïve cells can enter (Fig. 8). A similar, but less pronounced, effect is seen for CD8+ T cells.
It has been documented that females have a higher incidence of autoimmune diseases both in humans and mice 40,41. NOD females are known to have a higher burden of islet infiltrates than males of the same age, correlating with an earlier onset of overt diabetes 4. The composition of islet-infiltrating lymphocytes in individual males and females has not previously been compared. We compared age-matched groups of male and female NOD mice and because of the disparity of islet inflammation between these two groups, we also compared the mice individually, based on their level of islet inflammation.
We found a surprisingly large percentage of B cells in the islets of both male and female NOD mice. This has been previously reported in female NOD mice but not in males 29,42. We report here that a large pool of B cells was present in the islets even as female NOD mice became diabetic and the tight relationship between the CD8+ and CD4+ T cells in the islets was maintained.
Despite the disparity in the level of inflammation, NOD males were similar to females in the tight control of the CD4+:CD8+ ratio and the CD4+ T cell:B cell ratio in the islets. Very old males attained levels of islet infiltrates similar to or greater than those seen in 12 week-old NOD females and with strictly controlled CD4+:CD8+ T cell ratios. This observation indicates that inflammation develops more slowly in males but in a similar manner. Indeed, in many NOD colonies the males can develop a significant incidence of diabetes43.
Progression of β cell autoimmunity with a fixed ratio of CD4+ and CD8+ T cells is puzzling. One possibility is that T cells in the islets are in equilibrium with the rest of the immune system, but this goes against the idea that entry into the islets is only accomplished by T cells that are activated in the PLN. That theory would require the lymph node to activate the appropriate ratios of CD4+ and CD8+ T cells. The tertiary lymphoid structure hypothesis posits that structures form in the islets that are similar to lymph nodes and in equilibrium with the rest of the body. If this is the case, a stringently controlled CD4+:CD8+ T cell ratio would be expected. However, a tightly controlled T cell:B cell ratio would also be expected and twice the level of B cells was found in the islets compared to the lymph nodes (Fig. 1B and D).
It has been shown that induction of IL-4+ CD4+ T cells can significantly delay the onset of diabetes and constitutive expression of IL-4 in the islet cells abrogates insulitis 37,38. Paradoxically, IL-4 knockout NOD mice have a normal onset of diabetes 44. We found that male NOD mice as a group had higher percentages of IL-4 competent CD4+ T cells in their islet-infiltrating CD4+ T cell pool than their female counterparts. However, when examined as a continuum of increasing inflammation, it was obvious that mice with very low levels of islet inflammation had high percentages of IL-4 competent cells in their infiltrating CD4+ T cell pool regardless of sex. In both male and female NOD mice, the contribution of IL-4+ expressing cells to the CD4+ T cell pool was considerably reduced early as diabetogenesis progressed, indicating that the differences were a result of the level of inflammation and not a characteristic of male or female. Bao et al. previously observed that, when stimulated in vitro, islet-infiltrating CD4+ T cells from 4 week-old male NOD mice produced more IL-4 than those from 4 week-old female NOD mice 10. Our results support this result, since low levels of inflammation were seen in very young male NOD mice, so the percentage of CD4+ T cells competent to express IL-4 can be quite high. The same study found that by 10 weeks the islet-infiltrating CD4+ T cells of male and female NOD mice produced equivalent amounts of IL-4 when stimulated in culture. Here we show that as the infiltrate in the islets increases, the percent of IL-4 competent T cells in the islets falls to 3% of the CD4+ T cells pool and is maintained at that level for males and females. This indicates that IL-4 competent CD4+ T cells are highly regulated in the islets during diabetogenesis. A novel finding of this study is the predictable composition of IL-4 competent CD4+ T cells, CD4+ T cells and CD8+ T cells in the islets as diabetogenesis progresses and the linear relationship between these components. It will be of great interest to know if treatments that cure diabetes in NOD mice and increase the percentage of IL-4 expressing T cells in the islets do so by decreasing the inflammation which results indirectly in an increase in IL-4 competent CD4+ T cells.
Tregs are also capable of suppressing inflammation. Given the decreased incidence of T1D in male NOD mice, one possibility was that males have higher levels of Treg. Contrary to these expectations, young female NOD mice had higher levels of Tregs in their islets than their male counterparts, although older female mice had slightly reduced levels of Tregs than their male counterparts. On the other hand, in very old male NOD mice the percentage of Treg had dropped substantially from the level of 12 week NOD males. When we examined the data on a continuum, levels of Tregs were highest early in disease and decreased slowly as inflammation continued to increase. These findings are in agreement with earlier work demonstrating that in NOD female mice FoxP3+ CD4+ T cells in the PLN and islets decline with age, while the FoxP3+ cells in the spleen do not 28,31. Again, changes in the frequency of FoxP3+ CD4+ T cells may be a result of the level of islet inflammation and not the sex of the NOD mice.
IGRP-specific CD8+ T cells are diabetogenic and have been used to predict the onset of diabetes 45,46. Accordingly, we anticipated male NOD mice might not have IGRP-specific CD8+ T cells. When grouped, female NOD mice did have much higher numbers of IGRP-specific CD8+ T cells. However, the number of IGRP+ T cells per islet in 27 week-old male NOD mice was comparable to that of the 12–14 week-old females. When we examined IGRP-specific T cells as percentage of the islet CD8+ T cell pool, female mice were not significantly different from male NOD mice. Next we examined the phenotype of the IGRP-specific CD8+ T cells to see if they were antigen experienced. As expected, the IGRP-specific CD8+ T cells in the islets of females were CD44hi CD62Llo effector cells, while those in the lymph nodes and spleen were CD62Lhi memory or naïve cells. The same distribution was also seen in males. Again, the only differences between the male and female populations of IGRP-specific CD8+ T cells were attributable to the total number of infiltrating cells. Enee et. al. recently reported similar results for male and female NOD mice expressing HLA-A2 as a trans gene, demonstrating that HLA-A2 had no effect of the Kd-restricted IGRP responses 47. These findings in males are similar to that reported here. Hence, there was no evidence of selective recruitment of IGRP-specific CD8+ T cells in female NOD mice.
One important observation from this study is the presence of large numbers of naïve T cells in the islets. It had been previously thought that T cells infiltrating the islets were largely if not exclusively activated, diabetogenic effectors. We found a large number of both naïve CD4+ and naïve CD8+ T cells. Thus the islets may correspond to the beginnings of “lymph node-like” structures seen in the pancreas of mice with advanced disease. Apparently the cells making up these lymphoid structures can sequester naïve T cells. We also observed a large pool of B cells infiltrating the islets, in agreement with others 29. B cells are required for the development of diabetes and have been shown to be required for epitope spreading 48. In mucosal tissue it has also been demonstrated that lymphotoxin produced by B cells can drive the formation of lymphoid structures 49. The present study indicates that large numbers of both B cells and naïve T cells are present in the islets in an increasingly inflammatory environment. The large population of naïve T cells may be involved in epitope spreading seen later where new autoantigen are recognized, and priming does not occur in the draining lymph node, but takes place in the lymphoid structures in the islets. Thus priming could occur in a more inflammatory environment.
The differences within the islets of male and female and young and old NOD mice did not appear to be discrete. Islet infiltrates in male NOD mice contained levels of CD8+ T cells, B cells, Th2, Treg, and IGRP reactive T cells comparable to those found in females at any set level of inflammation, as defined by the number of CD4+ T cells per islet. In addition, NOD male and female mice both had large pools of naïve T cells and B cells in their islets. Our data suggest that the processes are similar in male and female mice, but that the rates of progression differ. Indeed NOD/LtJ males ultimately developed diabetes at a 70% incidence, though not in the normally allotted 20 weeks 43. Our data also indicate diabetogenesis in the islets progresses with predictable levels of some lymphocytes. If the number of islets and number of CD4+ T cells harvested from the islets is known for an individual NOD mouse we offer formulas to predict the number of CD8+ T cells, IL-4 competent CD4+ T cells, naïve CD8+ T cells and naïve CD4+ T cells that are present.
In this manuscript we have focused on the immune system mediated aspects of diabetogenesis and the differences between males and females. We were able to show similar immune cells accumulating in islets, but at different rates. We argue that the differences between males and females are not due to qualitative differences in the autoimmune response. We also indentified large pools of apparently naïve CD4+ and CD8+ T cells, which in the presence of B cells in the islets, could contribute to epitope spreading.
Supplemental Figure 1
The incidence of diabetes in female NOD/LtJ mice from Jackson Labs in our animal facility.
Results are shown for 20 female NOD mice. Blood glucose of mice was monitored weekly and mice were considered diabetic when they had 2 consecutive blood sugar readings over 250 mg/dL. The median age of overt diabetes was 16 weeks, similar to Jax females, 15 weeks, plotted on the same graph 43.
Supplemental Figure 2
Dot plots of islet-infiltrating lymphocytes from individual NOD mice.
(A) Lymphocytes isolated from the islets of one individual 12 week-old female NOD mouse were analyzed by flow cytometry using the gating scheme shown above. A total of 16 378 CD4+ T cells, 5068 CD8+ T cells and 25 401 CD19+ B cells were analyzed from 148 islets isolated from mouse A. Therefore mouse A had 111 CD4+ T cells/islet, 34 CD8+ T cells/islet and 172 CD19+ B cells per islet.
(B) Lymphocytes were isolated from the islets of one individual 8 week-old female IL-4 reporter NOD mouse and analyzed by flow cytometry using the gating scheme shown above. A total of 16 472 CD4+ T cells, 4457 CD8+ T cells and 6899 CD19+ B cells were analyzed from 81 islets isolated from mouse B. Therefore mouse B had 203 CD4+ T cells/islet, 55 CD8+ T cells/islet and 85 CD19+ B cells per islet.
Supplemental Figure 3
A line describes a relationship between 2 variables. This can be written as Y=slope(X) + Y-intercept, where X and Y represent 2 different variables and the Y-intercept is the value of Y when X equals zero. In the present manuscript, the Y-intercept does not represent an actual data point; instead it is a theoretical extension of the predicted line. If the Y-intercept is zero, the ratio between the X and Y remains the same at all points and Y/X equals the slope. If the Y-intercept is greater than zero, the ratio, between X and Y, changes with different values of X. Y/X is larger for low values of X and approaches a constant value for large values of X. The line Y=0.03X+0.10 is graphed above in blue. This is the line that describes the relationship between IL-4 producing CD4+ T cells and CD4+ T cells, where Y = the number of IL-4 producing CD4+ T cells per islet and X = the number of CD4+ T cells. The predicted percent of Y in the X population, or 100(Y/X), is graphed in blue triangles. The resulting percentages resemble the measured percentages of IL-4 producing cells in the CD4+ T cells population (see Figure 3D). The line Y=0.03X+0.0 is graphed above in orange. The predicted percent of Y in the X population by this formula is graphed in orange diamonds and is always 3%.
Supplemental Table 2
Raw data and calculations for Figure 3. Islets were isolated from individual mice and counted. After overnight incubation at 37°C, the entire sample was analyzed by flow cytometry. The number of CD3+CD4+ T cells and GFP+CD3+CD4+ T cells was recorded for each sample. Calculations are indicated in the column heading.
The expertise and assistance of Lucinda Hensley, Shaun Steel, Corey Morris and Michael Johnson was invaluable. This research is supported in part by National Institutes of Health Grants AI 0524354, AI052435-03S1, AI058014 and AI54843 and Grant 1-2008-24 from the Juvenile Diabetes Research Foundation. The work described in this article was carried out in accordance with the EC Directive 86/609/EEC for animal experiments and The Uniform Requirements for Manuscripts Submitted to Biomedical Journals.