Brelje T C, Sorenson R L
Department of Cell Biology and Neuroanatomy, University of Minnesota Medical School, Minneapolis 55455.
Endocrinology. 1991 Jan;128(1):45-57. doi: 10.1210/endo-128-1-45.
This study investigated the effects of homologous rat PRL (rPRL) and rat GH (rGH) on islet growth as indicated by modifications in insulin secretion, islet cell proliferation, and islet volume with neonatal and adult rat islets in vitro. The number of proliferating cells was determined by immunocytochemical staining for 5-bromo-2'-deoxyuridine (BrdU) incorporated into replicating DNA during the final 24 h of culture. When neonatal rat islets were examined by laser scanning confocal microscopy, more than 90% of the BrdU-labeled nuclei were observed in B-cells with insulin immunoreactivity. In neonatal rat islets, rPRL was much more effective than rGH in increasing insulin secretion (3.7-fold vs. 1.4-fold) during the 10 days of culture. The number of BrdU-labeled nuclei per islet was increased from 2.9 +/- 0.4 (n = 77) in control islets to 47.3 +/- 2.7 (n = 95) with rPRL (16.3-fold) and 9.7 +/- 0.8 (n = 84) with rGH (3.3-fold). The effects of rPRL and rGH on both insulin secretion and BrdU labeling were approximately additive. After 10 days, an increased average islet volume was only observed with rPRL. When followed for 36 days, the total amount of islet tissue was unchanged for control islets (1.1-fold), more than doubled with rPRL (2.5-fold), and only slightly increased with rGH (1.4-fold). From the observed rates of islet cell proliferation and increases in islet volumes, doubling times of 23-24 days for rPRL and 89-91 days for rGH can be estimated. Of other proposed islet growth factors, cholecystokinin, epidermal growth factor, platelet-derived growth factor, and 2-aminoisobutyric acid, an increase in insulin secretion and islet cell proliferation was only observed with cholecystokinin in neonatal rat islets. However, both effects were less than 20% of those observed with rPRL. In adult rat islets, rPRL was also more effective than rGH in increasing insulin secretion (1.6-fold vs. 1.2-fold) during the 9 days of culture. The number of BrdU-labeled nuclei per islet was increased from 2.7 +/- 0.5 (n = 96) in control islets to 9.5 +/- 0.6 (n = 175) with rPRL (3.5-fold). In contrast to the neonatal islets, rGH had no effect on the number of BrdU-labeled nuclei per islet in adult rat islets (2.4 +/- 0.3, n = 194).(ABSTRACT TRUNCATED AT 400 WORDS)
本研究通过体外观察新生大鼠和成年大鼠胰岛胰岛素分泌、胰岛细胞增殖及胰岛体积的变化,探究了同源大鼠催乳素(rPRL)和大鼠生长激素(rGH)对胰岛生长的影响。增殖细胞数量通过免疫细胞化学染色检测培养最后24小时掺入复制DNA中的5-溴-2'-脱氧尿苷(BrdU)来确定。用激光扫描共聚焦显微镜检查新生大鼠胰岛时,超过90%的BrdU标记细胞核见于有胰岛素免疫反应性的B细胞。在新生大鼠胰岛中,培养10天期间rPRL在增加胰岛素分泌方面比rGH有效得多(3.7倍对1.4倍)。每个胰岛BrdU标记细胞核的数量从对照胰岛的2.9±0.4(n = 77)增加到rPRL处理后的47.3±2.7(n = 95)(16.3倍)和rGH处理后的9.7±0.8(n = 84)(3.3倍)。rPRL和rGH对胰岛素分泌和BrdU标记的影响大致是相加的。10天后,仅rPRL处理的胰岛平均体积增加。培养36天时,对照胰岛的胰岛组织总量无变化(1.1倍),rPRL处理的增加了一倍多(2.5倍),rGH处理的仅略有增加(1.4倍)。根据观察到的胰岛细胞增殖率和胰岛体积增加情况,可估计rPRL的倍增时间为23 - 24天,rGH为89 - 91天。在其他提出的胰岛生长因子中,胆囊收缩素、表皮生长因子、血小板衍生生长因子和2-氨基异丁酸,仅在新生大鼠胰岛中观察到胆囊收缩素能增加胰岛素分泌和胰岛细胞增殖。然而,这两种效应均不到rPRL所观察到效应的20%。在成年大鼠胰岛中,培养9天期间rPRL在增加胰岛素分泌方面也比rGH更有效(1.6倍对1.2倍)。每个胰岛BrdU标记细胞核的数量从对照胰岛的2.7±0.5(n = 96)增加到rPRL处理后的9.5±0.6(n = 175)(3.5倍)。与新生胰岛不同,rGH对成年大鼠胰岛中每个胰岛BrdU标记细胞核的数量无影响(2.4±0.3,n = 194)。(摘要截于400字)