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发育年龄或移植后时间对近交系Fischer大鼠支持细胞数量和睾丸大小的影响。

Effect of developmental age or time after transplantation on Sertoli cell number and testicular size in inbred Fischer rats.

作者信息

Johnson L, Suggs L C, Norton Y M, Zeh W C

机构信息

Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Faculty of Toxicology.

出版信息

Biol Reprod. 1996 May;54(5):948-59. doi: 10.1095/biolreprod54.5.948.

Abstract

The objectives were to establish the developmental age of Fischer rats at which the Sertoli cell number is stabilized, to establish the normal reference plateau number of Sertoli cells for evaluation of testes after transplantation, and to determine whether the developmental pattern establishing Sertoli cell proliferation and stability are similar between intact and transplanted testes. Sertoli cell number was determined at ages 1--120 days in intact rats and at various times (10-90 days) after transplantation of prenatal or neonatal tests. Tests were fixed by vascular perfusion or by immersion with 2% glutaraldehyde and and immersion in 1% osmium and were embedded in Epon 812. Sections and serial sections were cut at 0.5 micrometer to determine the Sertoli cell nuclei volume density and the volume of an individual Sertoli cell nucleus by brightfield microscopy or at 20 micrometers to determine the maximum height and width of nuclei. A correction factor was calculated for intact (0.663 +/- 0.025) or for transplanted (0.558 +/- 0.029) testes to determine the volume of a single Sertoli cell nucleus from height and width measurements. In intact testes, Sertoli cell numbers significantly increased to Day 20 but were not different between 15 and 90 days. Sertoli cell number in prenatal or neonatal transplanted testes increased to 20 or 30 days posttransplantation and then stabilized to Day 60 or 90. There was no difference in the plateau number of Sertoli cells per rat between prenatal and neonatal testes. Sertoli cells in 10-day- and 30-day-transplanted testes incorporated 3H-thymidine when placed in culture. A few tubules had complete spermatogenesis at 90 days posttransplantation, indicating that Sertoli cells in some of these tubules were functional. Leydig cell structure appeared to be normal. Leukocytic infiltration of testes was not observed in intact rats or in rats receiving neonatal testes. Although transplanted testes showed a delay in reaching the plateau value for Sertoli cell number per testis and although the value reached was lower, the developmental pattern of Sertoli cell proliferation in transplanted testes was similar to that in intact rats.

摘要

本研究的目的是确定Fischer大鼠支持细胞数量稳定时的发育年龄,建立用于评估移植后睾丸的支持细胞正常参考平台数量,并确定完整睾丸和移植睾丸之间建立支持细胞增殖和稳定性的发育模式是否相似。在完整大鼠的1至120天龄时以及产前或新生儿睾丸移植后的不同时间(10至90天)测定支持细胞数量。睾丸通过血管灌注或用2%戊二醛浸泡固定,然后用1%锇酸浸泡,并嵌入Epon 812中。切片和连续切片切成0.5微米厚,通过明场显微镜确定支持细胞核体积密度和单个支持细胞核的体积,或切成20微米厚以确定细胞核的最大高度和宽度。计算完整睾丸(0.663±0.025)或移植睾丸(0.558±0.029)的校正因子,以便根据高度和宽度测量确定单个支持细胞核的体积。在完整睾丸中,支持细胞数量在第20天显著增加,但在15至90天之间没有差异。产前或新生儿移植睾丸中的支持细胞数量在移植后第20或30天增加,然后在第60或90天稳定。产前和新生儿睾丸之间每只大鼠的支持细胞平台数量没有差异。10天和30天移植睾丸中的支持细胞在培养时掺入了3H-胸腺嘧啶。移植后90天,一些小管有完整的精子发生,表明这些小管中的一些支持细胞是有功能的。间质细胞结构似乎正常。在完整大鼠或接受新生儿睾丸的大鼠中未观察到睾丸的白细胞浸润。尽管移植睾丸在达到每个睾丸支持细胞数量的平台值方面出现延迟,并且尽管达到的值较低,但移植睾丸中支持细胞增殖的发育模式与完整大鼠相似。

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