Histomorphology and ultrastructure of pancreatic islet tissue during in vivo maturation of rat pancreas

被引:21
作者
De Franca Carvalho, Carolina Prado
Rebelo Martins, Junia Carolina
Da Cunha, Daniel Andrade
Boschero, Antonio Carlos
Collares-Buzato, Carla Beatriz [1 ]
机构
[1] Univ Estadual Campinas, Inst Biol, Dept Histol & Embyol, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Inst Biol, Dept Physiol & Biophys, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
differentiation; endocrine pancreas; insulin secretion; postnatal; development; morphology;
D O I
10.1016/j.annat.2005.10.009
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 [人体解剖与组织胚胎学];
摘要
In this study, we have investigated the structural and ultrastructural features of pancreatic islet tissue during rat postnatal development. For this purpose, we used neonatal (1-2 days old), young (21 days old) and adult (3-4 months old) rats. From a functional point of view, neonatal islet tissue displayed a relatively poor insulin secretary response to glucose stimulation in comparison with the adult ones. Histological analysis showed that neonatal islet cells display a less organized morphology in comparison with the young and adult ones, characterized by a less defined form and the presence of ductal structures within or nearby the islet. Regarding the islet cytoarchitecture, no differences were observed among at[ animal groups studied. B-cells were always typically detected within the islet core while A-cells occupied the islet periphery area. No marked differences were found during postnatal animal development regarding the uttrastructural aspect of the endocrine cells and their secretary granules. Nevertheless, quantitative analysis showed a lower B-cell/non-B-cell ratio, a higher association with ducts and an increased immunoreaction for proliferating cell nuclear antigen (PCNA) in neonatal islets as compared to young and adults. In conclusion, the acquisition of an adult pattern of insulin secretion may require an appropriate histoarchitecture and B-cell/non-B-cell proportion that may affect crucial regulatory events such as the paracrine and/or the cell-cell interaction or communication within the islet. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:221 / 234
页数:14
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