Hänninen A, Salmi M, Simell O, Jalkanen S
National Public Health Institute, Turku, Finland.
Diabetes. 1996 Sep;45(9):1173-80. doi: 10.2337/diab.45.9.1173.
The mucosal addressin cell adhesion molecule-1 (MAdCAM-1) becomes expressed on islet vessels of NOD mice early during lymphocyte accumulation in islets. Because MAdCAM-1 preferentially mediates the homing of mucosal lymphocytes, islet-associated MAdCAM-1 could favor the accumulation of mucosal lymphocytes in pancreatic islets. Therefore, we investigated the relative frequency of islet-infiltrating lymphocytes with a mucosal phenotype (alpha 4/beta 7-integrinhigh and L-selectinlow) at early and advanced stages of insulitis. We found that until the age of 12 weeks, lymphocytes with a mucosal phenotype were particularly frequent in the pancreas (percentage of beta 7-integrinhigh-lymphocytes was 48% at 8 weeks and 73% at 12 weeks), whereas in diabetic mice older than 16 weeks, their relative number was smaller (26% of pancreas-infiltrating lymphocytes). To define the origin and homing behavior of beta 7-integrinhigh-lymphocytes before their accumulation in pancreatic islets in NOD mice, we sought for such lymphocytes in different lymphoid organs and studied their recirculation. We found that compared with lymphocytes in several other strains, in NOD mice such lymphocytes were most frequent in nonmucosal lymphoid tissues (peripheral and pancreatic lymph nodes, spleen) from an early age. When injected to blood circulation, mucosal beta 7high-lymphocytes failed to home efficiently back to mucosal lymphoid tissue in NOD mice but homed aberrantly to nonmucosal lymphoid tissues. After adoptive transfer of diabetogenic splenocytes, the first lymphocytes accumulating in the pancreas were predominantly beta 7-integrinhigh. We conclude that mucosa-associated lymphocytes are involved in the early phases of islet-inflammation in NOD mice and that the aberrant homing behavior of lymphocytes expressing high levels of beta 7-integrin may associate with their accumulation in pancreatic islets early during insulitis.
黏膜定居素细胞黏附分子-1(MAdCAM-1)在淋巴细胞开始在胰岛中聚集的早期,就表达于NOD小鼠的胰岛血管上。由于MAdCAM-1优先介导黏膜淋巴细胞的归巢,胰岛相关的MAdCAM-1可能有利于黏膜淋巴细胞在胰腺胰岛中的聚集。因此,我们研究了在胰岛炎早期和晚期具有黏膜表型(α4/β7整合素高表达和L-选择素低表达)的胰岛浸润淋巴细胞的相对频率。我们发现,在12周龄之前,具有黏膜表型的淋巴细胞在胰腺中特别常见(8周龄时β7整合素高表达淋巴细胞的百分比为48%,12周龄时为73%),而在16周龄以上的糖尿病小鼠中,它们的相对数量较少(胰腺浸润淋巴细胞的26%)。为了确定NOD小鼠β7整合素高表达淋巴细胞在聚集到胰腺胰岛之前的来源和归巢行为,我们在不同的淋巴器官中寻找此类淋巴细胞并研究它们的再循环。我们发现,与其他几个品系的淋巴细胞相比,在NOD小鼠中,此类淋巴细胞从幼年起就在非黏膜淋巴组织(外周和胰腺淋巴结、脾脏)中最为常见。当注入血液循环时,黏膜β7高表达淋巴细胞在NOD小鼠中不能有效地归巢回到黏膜淋巴组织,而是异常地归巢到非黏膜淋巴组织。在致糖尿病性脾细胞过继转移后,最早在胰腺中聚集的淋巴细胞主要是β7整合素高表达的。我们得出结论,黏膜相关淋巴细胞参与了NOD小鼠胰岛炎症的早期阶段,并且表达高水平β7整合素的淋巴细胞的异常归巢行为可能与其在胰岛炎早期在胰腺胰岛中的聚集有关。