Cole Beth, Hensinger Krista, Maciel Gustavo A R, Chang R Jeffery, Erickson Gregory F
Department of Reproductive Medicine, University of California, San Diego, La Jolla, California 92093-0633, USA.
J Clin Endocrinol Metab. 2006 Sep;91(9):3654-61. doi: 10.1210/jc.2006-0641. Epub 2006 Jul 5.
The purpose of this research was to characterize the spatiotemporal expression of P450c17 in the human fetal ovary.
P450c17 protein was visualized in sections of control and anencephalic ovaries using immunohistochemistry.
Subjects included control (nonanencephalic) and anencephalic human fetal ovaries during the second and third trimesters.
In second-trimester control ovaries, P450c17 was highly expressed in primary interstitial cells (PIC) located between the ovigerous cords near the cortical-medullary border where meiosis and primordial follicle formation were occurring. Morphometric analysis revealed a progressive decrease in the number of PIC during the second trimester, suggesting that PIC might have a finite lifetime. Between 25 and 32 wk, relatively few cells stained positive for P450c17; however, after 33 wk, P450c17 was strongly expressed in theca interstitial cells (TIC) bordering developing follicles. Surprisingly, the TIC appeared remarkably early during folliculogenesis, e.g. as early as the primary-to-secondary transition, and exhibited notable hyperplasia throughout preantral and early antral follicle growth. Owing to large numbers of developing preantral follicles, the third trimester was characterized by an increased abundance of P450c17-positive TIC. During this time period, P450c17 was strongly expressed in the hilus interstitial cells juxtaposed to the rete ovarii. Studies of ovaries of anencephalic fetuses revealed a similar spatiotemporal pattern of P450c17 expression in the PIC, TIC, and hilus interstitial cells, consistent with the possibility that pituitary hormones may not be involved in P450c17 expression in fetal ovaries.
We identified three different classes of P450c17-expressing interstitial cells in the human fetal ovary, each having a different spatiotemporal pattern of P450c17 expression and, presumably, a different set of physiological functions.
本研究旨在描述细胞色素P450c17在人胎儿卵巢中的时空表达特征。
采用免疫组织化学方法,在对照和无脑儿卵巢切片中观察细胞色素P450c17蛋白。
研究对象包括孕中期和孕晚期的对照(非无脑儿)和无脑儿人胎儿卵巢。
在孕中期对照卵巢中,细胞色素P450c17在靠近皮质-髓质边界、正在进行减数分裂和原始卵泡形成的生卵索之间的初级间质细胞(PIC)中高度表达。形态计量分析显示,孕中期PIC数量逐渐减少,提示PIC可能具有有限的寿命。在25至32周之间,相对较少的细胞细胞色素P450c17染色呈阳性;然而,33周后,细胞色素P450c17在与发育中的卵泡相邻的卵泡膜间质细胞(TIC)中强烈表达。令人惊讶的是,TIC在卵泡发生过程中出现得非常早,例如早在初级卵泡向次级卵泡转变时就出现,并在整个窦前卵泡和早期有腔卵泡生长过程中表现出明显的增生。由于大量发育中的窦前卵泡,孕晚期细胞色素P450c17阳性TIC的丰度增加。在此期间,细胞色素P450c17在与卵巢网相邻的门间质细胞中强烈表达。对无脑儿胎儿卵巢的研究显示,PIC、TIC和门间质细胞中细胞色素P450c17表达的时空模式相似,这与垂体激素可能不参与胎儿卵巢中细胞色素P450c17表达的可能性一致。
我们在人胎儿卵巢中鉴定出三类表达细胞色素P450c17的间质细胞,每类细胞具有不同的细胞色素P450c17表达时空模式,推测具有不同的生理功能。