|Home | About | Journals | Submit | Contact Us | Français|
Pancreatic islet transplantation is a highly promising approach for the treatment of insulin-dependent diabetes mellitus. However, the procedure remains experimental for several reasons, including its low efficiency caused by the early graft loss of transplanted islets. We demonstrate that Gr-1+CD11b+ cells generated by transplantation and their IFN-γ production triggered by Vα14 NKT cells are an essential component and a major cause of early graft loss of pancreatic islet transplants. Gr-1+CD11b+ cells from Vα14 NKT cell–deficient (Jα281−/−) mice failed to produce IFN-γ, resulting in efficient islet graft acceptance. Early graft loss was successfully prevented through the repeated administration of α-galactosylceramide, a specific ligand for Vα14 NKT cells, resulting in dramatically reduced IFN-γ production by Gr-1+CD11b+ cells, as well as Vα14 NKT cells. Our study elucidates, for the first time, the crucial role of Gr-1+CD11b+ cells and the IFN-γ they produce in islet graft rejection and suggests a novel approach to improving transplantation efficiency through the modulation of Vα14 NKT cell function.
Patients with insulin-dependent diabetes mellitus regularly fail to achieve insulin independence after transplantation of islets from a single donor pancreas because of early graft loss (1, 2). Early islet loss is estimated to occur in ≤50% of the transplanted islet mass (3) and occurs at similar frequencies in both allogeneic and syngeneic combinations in a mouse model, possibly because of stress, inflammation, or innate responses caused by transplantation. To analyze the mechanisms of early islet loss, the syngeneic islet transplantation model is advantageous because allogeneic immune responses are avoidable.
After transplantation into the recipient liver, islet grafts are lodged together in the periphery of the portal vein as emboli, causing ischemic degeneration of the corresponding areas. This may trigger innate immune responses resulting in the release of inflammatory cytokines harmful to islet grafts. Insulin-secreting β cells have been shown to be susceptible in vitro to exposure to proinflammatory cytokines such as IFN-γ, TNF-α, and IL-1β (4), and it is likely that proinflammatory cytokines are also a major cause of islet graft failure in vivo.
Vα14 NKT cells belong to a distinct subset of lymphocytes bridging the innate and acquired immune systems and play an important role in the immediate responses, because Vα14 NKT cells produce large amounts of IFN-γ immediately after activation, which in turn activates NK cells and other cells in the innate immune system and CD4 Th1 cells and CD8 cytotoxic T cells in the acquired immune system (5–9). Thus, Vα14 NKT cells serve as a front line defense against various bacteria, viruses, fungi, and intracytoplasmic parasites (5, 6).
Because Vα14 NKT cells are relatively abundant in the liver, the site of choice for islet transplantation, and because IFN-γ is believed to be an important factor in the destruction of islet β cells, we hypothesized that Vα14 NKT cells in the liver might be involved in islet graft failure. We demonstrate that, in mice, IFN-γ–producing Gr-1+CD11b+ cells and Vα14 NKT cells are major components of the early graft loss of transplanted islets and the low efficiency of pancreatic islet transplants. Our findings provide an approach to improve transplant efficiency through the modulation of Vα14 NKT cell function.
To test the possibility that Vα14 NKT cells are involved in islet graft failure, we attempted to establish an experimental system of islet transplantation. We first examined the minimum number of donor islets required to ameliorate hyperglycemia in streptozotocin (STZ)-induced diabetic mice. C57BL/6 mice became hyperglycemic and diabetic soon after the i.v. injection of STZ (Fig. 1 A). In STZ-induced diabetic mice, 400 syngeneic islets transplanted into the liver were found to be sufficient to achieve normoglycemia (Fig. 1 B, left), whereas normoglycemia could not be achieved by the transplantation of 200 syngeneic islets, the number of islets that can be isolated from a single mouse pancreas (Fig. 1 C, left). In agreement with biochemical data, intact islets with well-granulated β cells were histologically seen in mice receiving 400 islets, whereas damaged islets with degranulated β cells were observed in mice receiving 200 islets (Fig. 1, B and C, right).
We then investigated whether Vα14 NKT cells are involved in early islet graft loss. All diabetic Jα281−/− mice became normoglycemic by day 11 after transplantation of 200 or even 100 islets (Fig. 1, D and E, left). Histological examination also clearly demonstrated the existence of intact islet grafts with well-granulated β cells (Fig. 1 D, right), suggesting that Vα14 NKT cells are responsible for graft rejection of transplanted islets.
To prove the deleterious effects of Vα14 NKT cells on grafted islets, 5 × 106 liver mononuclear cells isolated from naive WT, Jα281−/−, or IFN-γ–deficient mice were injected at the time of transplantation into the portal vein of diabetic Jα281−/− mice receiving 200 syngeneic islets. Diabetic Jα281−/− mice injected with cells from WT mice remained hyperglycemic 60 d after transplantation (Fig. 1 F, left), whereas those with cells from Jα281−/− or IFN-γ–deficient mice became normoglycemic (Fig. 1, G and H, left). Histological examination also proved the existence of intact islets in the recipients of cells from Jα281−/− or IFN-γ–deficient mice, but not from WT mice (Fig. 1, F–H, right). The results suggest that Vα14 NKT cells and IFN-γ are essential components of early graft failure.
To elucidate cellular changes associated with islet graft failure, hepatic mononuclear cells were isolated periodically after islet transplantation and examined by FACS using α-galactosylceramide (α-GalCer)–loaded CD1d (α-GalCer–CD1d) tetramers. FACS analysis showed that the percentage of α-GalCer–CD1d tetramer+ Vα14 NKT cells initially decreased from 10.3% at 0 h to ~5% at 6 h but then surged to 19.2% at 24 h after islet transplantation (Fig. 2 A, left). The findings indicate the activation of Vα14 NKT cells that down-modulate their receptor expression, resulting in the failure to detect Vα14 NKT cells by α-GalCer–CD1d tetramers, as reported previously (10–12). Furthermore, Vα14 NKT cells obtained at 2–6 h after transplantation produced inflammatory cytokines, such as IFN-γ and IL-1β (Fig. 2 A), suggesting that Vα14 NKT cells are activated by transplantation. After the disappearance of Vα14 NKT cells, Vα14 NKT cells expand rapidly, as shown in Fig. 2 A (24 h) and as previously reported (10–12). Interestingly, the proportion of α-GalCer–CD1d tetramer− cells producing high levels of INF-γ increased markedly from 0.5 to 14.3% at 6 h after islet transplantation (Fig. 2 A, left). The α-GalCer–CD1d tetramer− cells were further gated, analyzed for Gr-1 and CD11b expression in relation to IFN-γ production, and determined to be Gr-1+CD11b+ cells (Fig. 2 B). Gr-1+ CD11b+ cells were CD11c−, CD86−, MHC class II−, F4/80+/−, and CD68+/− (Fig. 2 C) and were neutrophils in morphology (Fig. 2 D), indicating that these cells are neutrophils. The neutrophils that infiltrated the transplanted islet (Fig. 2 D) are likely to be the effector cells, because the injection of antibodies against Gr-1 or CD11b prevented the rejection of islet transplants (Fig. 3).
In marked contrast to WT mice, the increase in IFN-γ–producing Gr-1+CD11b+ cells was not seen in Jα281−/− mice (Fig. 2 A, left), suggesting that the activation of Vα14 NKT cells after islet transplantation triggers the induction of IFN-γ production by Gr-1+CD11b+ cells. Note that no increase in IL-4–producing cells was observed regardless of the presence or absence of Vα14 NKT cells (Fig. 2 A, right).
It is well known that soon after activation with α-GalCer or IL-12, Vα14 NKT cells produce IFN-γ, which, in turn, stimulates IFN-γ secretion by other cells, such as NK cells or CD8 T cells (9, 13, 14). In fact, a single injection of α-GalCer dramatically augmented IFN-γ production in Gr-1+CD11b+ cells (see Fig. 5 D), suggesting that Vα14 NKT cells indeed activate Gr-1+CD11b+ cells to produce IFN-γ. It is thus likely that increased IFN-γ production by Gr-1+CD11b+ cells is a direct consequence of Vα14 NKT cell activation triggered by islet transplantation, although molecules responsible for the activation of Vα14 NKT cells remain to be determined.
Similar to IFN-γ–producing Gr-1+CD11b+ cells, IL-4–producing Gr-1+CD11b+ cells induced by aluminum hydroxide, when antigens precipitated by aluminum hydroxide are used for immunization, play an important role in B cell activation (15). Despite the similarities in antigen independence and importance in the immune responses of these two populations, several apparent differences are noted, such as the fact that IL-4–producing Gr-1+CD11b+ cells are evident 6 d after immunization, whereas IFN-γ–producing Gr-1+CD11b+ cells appear soon (6 h) after transplantation. The findings suggest functional diversity, although it is unclear whether the two populations are the same or different cells producing different cytokines at different time points.
In agreement with previously reported data (16), Vα14 NKT cells secreted large amounts of IFN-γ immediately after stimulation with α-GalCer but stopped producing IFN-γ after repeated α-GalCer stimulation (Fig. 4 A). Therefore, we hypothesized that repeated α-GalCer injections would modify IFN-γ production by Vα14 NKT cells and thus affect graft survival. To test this possibility, STZ-induced diabetic WT mice that had received 400 islets were treated once with vehicle at the time of transplantation; all mice became normoglycemic (Fig. 4 B). When diabetic WT mice that had received 400 islets were treated with a single 100-μg/kg injection of α-GalCer, none of the mice became normoglycemic even 60 d after transplantation (Fig. 4 C). In contrast, when WT mice were treated three times with 100 μg/kg α-GalCer on days 15, 11, and 7 before the induction of diabetes before islet transplantation, the transplantation of only 200 islets restored normoglycemia in all recipient mice within 10 d (Fig. 4 E). Mice treated with vehicle instead of α-GalCer remained hyperglycemic (Fig. 4 D). In agreement with our prediction, the results demonstrated that repeated α-GalCer injections before islet transplantation resulted in the down-regulation of IFN-γ production, which positively affected islet engraftment.
We investigated the effect of α-GalCer on the production of IFN-γ by Gr-1+CD11b+ cells. FACS analysis revealed that Gr-1+CD11b+ cells expanded rapidly after islet transplantation (Fig. 5 B) compared with nontransplanted controls (Fig. 5 A). The influx of Gr-1+CD11b+ cells is independent of Vα14 NKT cells because increased numbers of Gr-1+CD11b+ cells were detected in Jα281−/− mice after islet transplantation (Fig. 5 C), suggesting that Gr-1+CD11b+ cells are generated by transplantation. However, IFN-γ production by Gr-1+ CD11b+ cells was dramatically augmented by a single injection of α-GalCer (Fig. 5 D) but diminished to a level equivalent to the vehicle-treated control (Fig. 5 E) when repeated injections of α-GalCer were given (Fig. 5 F). Thus, IFN-γ production by Gr-1+CD11b+ cells is totally dependent on the activation status of Vα14 NKT cells. The findings on the protection of disease development by repeated α-GalCer injections were also reported in a type I diabetes model (17). It has been reported that IFN-γ is an essential molecule in the destruction of islets, causing the development of diabetes in a mouse model of virus-induced insulin-dependent diabetes mellitus (18). Furthermore, IFN-γ has been shown to induce nitric oxide–mediated toxicity to islet β cells in vitro in combination with IL-1 (19). It is thus likely that IFN-γ produced by Gr-1+CD11b+ cells might similarly affect islet β cells. Overall, our data suggest that the modulation of Vα14 NKT cell function by repeated α-GalCer stimulation in vivo manipulates IFN-γ production by Gr-1+CD11b+ cells and prevents immediate graft failure and the early loss of islet grafts, thus contributing to successful pancreatic islet transplantation.
Our results obtained in a mouse model have important clinical implications. Similar to Vα14 NKT cells in mice, human Vα24 NKT cells also release large quantities of INF-γ on activation (20), suggesting that the early graft loss of islets in humans is similarly mediated by Vα24 NKT cells. If this assumption is correct, treatment regimens aimed at the down-regulation of INF-γ production by human Vα24 NKT cells might help to prevent the early loss of islet grafts in clinical settings, even though Vα24 NKT cells are less frequent in the human liver (21), and, thus, might help to increase the efficiency of pancreatic islet transplants.
C57BL/6 mice were purchased from Charles River Laboratories and C57BL/6 Jα281−/− mice (10–15 wk old) raised in our facility were used (9). C57BL/6 IFN-γ–deficient mice were provided by Y. Iwakura (University of Tokyo, Tokyo, Japan) (22). Experimental plans were approved by the committee on institutional animal care and use at Fukuoka University and RIKEN.
Diabetes was induced by an i.v. injection of 180 mg/kg STZ (Sigma-Aldrich) (23).
α-GalCer was synthesized in our laboratory (27). Mice were injected i.p. one or three times with 100 μg/kg α-GalCer or 0.025% vehicle (wt/vol) before islet transplantation.
The following mAbs were used: anti–mouse FcRγII/III (2.4G2), FITC-conjugated anti-CD3 (145-2C11), FITC- or PE-conjugated anti-CD11b (M1/70), allophycocyanin-conjugated anti–IFN-γ (XMG1.2), allophycocyanin-conjugated anti–IL-4 (11B11), PerCP-conjugated anti–Gr-1 (Rb6-8c5), PerCP-Cy5.5–anti–Gr-1 (86-8C5), FITC–anti-CD11c (HL3), FITC–anti-CD86 (GL-1), FITC–anti–I-Ab (AF6-120.1), and controls (BD Biosciences). FITC–anti-F4/80 (A3-1) and FITC–anti-CD68 (FA-11) were obtained from SEROTEC. PE–α-GalCer–CD1d tetramers were prepared as previously described (28). For intracellular staining, cells were incubated with anti-FcRγII/III and neutravidin (Invitrogen), surface stained, fixed, permeabilized, stained with mAbs, and analyzed on a flow cytometer (FACSCalibur; Becton Dickinson). 10,000 viable cells were analyzed.
Hepatic mononuclear cells were prepared as described previously (25). Gr-1+CD11b+ cells and Vα14 NKT cells were sorted by MoFlo (DakoCytomation) with purity ≥99 and ≥98%, respectively. Splenic DCs were purified by MACS with anti-CD11c–coupled magnetic beads (Miltenyi Biotec) with purity ≥95%.
mAbs (10 μg/mouse) against Gr-1 or CD11b were i.p. injected into STZ-diabetic mice receiving 200 islets at the time of transplantation.
The liver and pancreas from transplant recipients were fixed in Bouin's solution, processed, and embedded in paraffin. Sections were stained with hematoxylin and eosin and aldehyde fuchsin. Immunohistochemistry was performed by a streptavidin–biotin–peroxidase complex method (29).
This work was supported by a grant (0211001) from the Central Research Institute of Fukuoka University (to Y. Yasunami); a Health Science Research Grant from the Ministry of Health, Labour and Welfare, Japan (to Y. Yasunami); a Grant-in-Aid (15390386) for Scientific Research (B) from the Japan Society for the Promotion of Science (to Y. Yasunami); and a Grant-in-Aid (13307011) for Scientific Research (A) from the Ministry of Education, Culture, Sports, Science and Technology, Japan (to M. Taniguchi).
The authors have no conflicting financial interests.