Size-related and size-unrelated functional heterogeneity among pancreatic islets

被引:16
作者
Aizawa, T
Kaneko, T
Yamauchi, K
Yajima, H
Nishizawa, T
Yada, T
Matsukawa, H
Nagai, M
Yamada, S
Sato, Y
Komatsu, M
Itoh, N
Hidaka, H
Kajimoto, Y
Hashizume, K
机构
[1] Shinshu Univ, Sch Med, Dept Aging Med & Geriatr, Matsumoto, Nagano 390, Japan
[2] Shinshu Univ, Sch Med, Dept Pathol, Matsumoto, Nagano 390, Japan
[3] Jichi Med Sch, Dept Physiol, Kawachi, Tochigi, Japan
[4] Kagoshima Univ, Fac Med, Dept Physiol, Kagoshima 890, Japan
[5] Shinshu Univ, Sch Med, Dept Lab Med, Matsumoto, Nagano 390, Japan
[6] Osaka Univ, Grad Sch Med, Dept Internal Med & Therapeut, Osaka, Japan
关键词
pancreatic beta cell; insulin; glucose sensitivity; islet architecture;
D O I
10.1016/S0024-3205(01)01332-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Functional heterogeneity of pancreatic islets was systematically analyzed for the first time using freshly isolated single rat pancreatic islets. First, 60 islets were sequentially exposed to 3, 9.4, 15.6, and 24.1 mM glucose for 30 min each in incubation experiments: 36 (60%) responded in a concentration-dependent and 19 (32%) in an all-or-none manner, and 5 (8%) islets did not respond to high glucose. As a group, the larger the islet, the higher the beta cell glucose sensitivity. However, glucose-stimulated elevation of [Ca2+](i) in the beta cell, insulin/glucagon ratio in the islet, and expression of glucose transporter 2, glucokinase, and pancreatic duodenal homeobox factor-1 in the P cell were not significantly related to islet size. Second, 50 islets were stimulated with 16.7 mM glucose in perfusion. A biphasic insulin release was found in 39 (78%), and no or little first phase response in 11 (22%) islets, irrespective of the islet size. Nevertheless, when the response was plotted as a group, it was clearly biphasic. Islet size, insulin content and the amount of insulin release were positively correlated with each other. In conclusion, there are size-related and size-unrelated functional diversity among pancreatic islets. The reason for such heterogeneity remained to be determined. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:2627 / 2639
页数:13
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