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成年雄性黑线毛足鼠的支持细胞并非终末分化:促卵泡激素对其增殖及连接蛋白组织的影响

Adult sertoli cells are not terminally differentiated in the Djungarian hamster: effect of FSH on proliferation and junction protein organization.

作者信息

Tarulli Gerard A, Stanton Peter G, Lerchl Alexander, Meachem Sarah J

机构信息

Prince Henry's Institute of Medical Research, Clayton Victoria, 3168, Australia.

出版信息

Biol Reprod. 2006 May;74(5):798-806. doi: 10.1095/biolreprod.105.050450. Epub 2006 Jan 11.

Abstract

Sertoli cell number is considered to be stable and unmodifiable by hormones after puberty in mammals, although recent data using the seasonal breeding adult Djungarian hamster (Phodopus sungorus) model challenged this assertion by demonstrating a decrease in Sertoli cell number after gonadotropin depletion and a return to control levels following 7 days of FSH replacement. The present study aimed to determine whether adult Sertoli cells are terminally differentiated using known characteristics of cellular differentiation, including proliferation, junction protein localization, and expression of particular maturational markers, in the Djungarian hamster model. Adult long-day (LD) photoperiod (16L:8D) hamsters were exposed to short-day (SD) photoperiod (8L:16D) for 11 wk to suppress gonadotropins and then received exogenous FSH for up to 10 days. Sertoli cell proliferation was assessed by immunofluorescence by the colocalization of GATA4 and proliferating cell nuclear antigen and quantified by stereology. Markers of Sertoli cell maturation (immature, cytokeratin 18 [KRT18]; mature, GATA1) and junction proteins (actin, espin, claudin 11 [CLDN11], and tight junction protein 1 [TJP1, also known as ZO-1]) also were localized using confocal immunofluorescence. In response to FSH treatment, proliferation was upregulated within 2 days compared with SD controls (90% vs. 0.2%, P < 0.001) and declined gradually thereafter. In LD hamsters, junction proteins colocalized at the basal aspect of Sertoli cells, consistent with inter-Sertoli cell junctions, and were disordered within the Sertoli cell cytoplasm in SD animals. Exogenous FSH treatment promptly restored localization of these junction markers to the LD phenotype. Protein markers of maturity remain consistent with those of adult Sertoli cells. It is concluded that adult Sertoli cells are not terminally differentiated in the Djungarian hamster and that FSH plays an important role in governing the differentiation process. It is proposed that Sertoli cells can enter a transitional state, exhibiting features common to both undifferentiated and differentiated Sertoli cells.

摘要

在哺乳动物中,人们认为青春期后支持细胞数量稳定,不受激素影响。然而,最近利用季节性繁殖的成年黑线仓鼠(Phodopus sungorus)模型获得的数据对这一观点提出了挑战,该研究表明促性腺激素缺乏后支持细胞数量减少,而在补充促卵泡激素(FSH)7天后恢复到对照水平。本研究旨在利用细胞分化的已知特征,包括增殖、连接蛋白定位和特定成熟标志物的表达,在黑线仓鼠模型中确定成年支持细胞是否终末分化。将成年长日照(LD)光周期(16小时光照:8小时黑暗)的仓鼠暴露于短日照(SD)光周期(8小时光照:16小时黑暗)11周以抑制促性腺激素,然后接受外源性FSH治疗长达10天。通过GATA4与增殖细胞核抗原的共定位免疫荧光法评估支持细胞增殖,并通过体视学进行定量分析。还使用共聚焦免疫荧光法对支持细胞成熟标志物(未成熟,细胞角蛋白18 [KRT18];成熟,GATA1)和连接蛋白(肌动蛋白、espin、紧密连接蛋白11 [CLDN11]和紧密连接蛋白1 [TJP1,也称为ZO-1])进行定位。与SD对照组相比,FSH治疗后2天内增殖上调(90%对0.2%,P < 0.001),此后逐渐下降。在LD仓鼠中,连接蛋白共定位于支持细胞的基底侧,与支持细胞间连接一致,而在SD动物的支持细胞胞质内则紊乱。外源性FSH治疗迅速将这些连接标志物的定位恢复到LD表型。成熟蛋白标志物与成年支持细胞的标志物一致。结论是,成年支持细胞在黑线仓鼠中并非终末分化,FSH在调控分化过程中起重要作用。有人提出,支持细胞可以进入一种过渡状态,表现出未分化和分化支持细胞共有的特征。

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