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甲状腺激素对大鼠青春期前支持细胞基底膜成分表达的调控

Regulation by thyroid hormone of the expression of basement membrane components in rat prepubertal Sertoli cells.

作者信息

Ulisse S, Rucci N, Piersanti D, Carosa E, Graziano F M, Pavan A, Ceddia P, Arizzi M, Muzi P, Cironi L, Gnessi L, D'Armiento M, Jannini E A

机构信息

Department of Experimental Medicine, University of L'Aquila, Italy.

出版信息

Endocrinology. 1998 Feb;139(2):741-7. doi: 10.1210/endo.139.2.5732.

Abstract

The present study reports the modulation of basement membrane (BM) components, laminin, entactin, and type IV collagen, expression in prepubertal rat Sertoli cell by the thyroid hormone T3. Immunocytochemical studies of permeabilized Sertoli cells in culture showed that T3 treatment (10[-7] M for 24 h) increased the number of cells staining positive for laminin and/or entactin (from 58 +/- 5.3% to 86.4 +/- 6.5%, P < 0.01). In contrast, a strong inhibition of type IV collagen immunopositivity was observed. Western blot analysis of Sertoli cell-conditioned media indicated that T3 treatment significantly (P < 0.01) increased the level of secreted entactin by 60-65% without affecting the levels of laminin A and B1/B2 chains. Moreover, thyroid hormone treatment of Sertoli cells significantly reduced type IV collagen secretion by 62% (P < 0.05). Slot blot analysis of poly-A RNA demonstrated a significant (P < 0.01) increase in the level of entactin messenger RNA (mRNA) by 140% (P < 0.01) and a 50% reduction of type IV collagen alpha1 chain mRNA after thyroid hormone treatment. No effect of the hormone was observed on the accumulation of the laminin B1 and B2 chain mRNAs in Sertoli cell cultures. These effects cannot be ascribed to changes in the degradation of BM components, because no effect of thyroid hormone was observed on plasminogen activators or metalloproteinase secretion by Sertoli cells. These observations indicate the Sertoli cell as a source of entactin within the testis, demonstrate the ability of T3 to differentially regulate the expression of BM components, and can be regarded as a part of the integrated mechanism by which thyroid hormone affects testicular development and differentiation.

摘要

本研究报道了甲状腺激素T3对青春期前大鼠支持细胞基底膜(BM)成分层粘连蛋白、巢蛋白和IV型胶原表达的调节作用。对培养的通透支持细胞进行免疫细胞化学研究表明,T3处理(10[-7]M,24小时)增加了层粘连蛋白和/或巢蛋白染色阳性的细胞数量(从58±5.3%增加到86.4±6.5%,P<0.01)。相反,观察到IV型胶原免疫阳性受到强烈抑制。对支持细胞条件培养基的蛋白质印迹分析表明,T3处理显著(P<0.01)使分泌的巢蛋白水平增加了60 - 65%,而不影响层粘连蛋白A和B1/B2链的水平。此外,甲状腺激素处理支持细胞使IV型胶原分泌显著减少了62%(P<0.05)。对poly - A RNA的狭缝印迹分析表明,甲状腺激素处理后,巢蛋白信使RNA(mRNA)水平显著(P<0.01)增加了140%(P<0.01),IV型胶原α1链mRNA减少了50%。在支持细胞培养物中未观察到该激素对层粘连蛋白B1和B2链mRNA积累的影响。这些效应不能归因于BM成分降解的变化,因为未观察到甲状腺激素对支持细胞纤溶酶原激活剂或金属蛋白酶分泌的影响。这些观察结果表明支持细胞是睾丸内巢蛋白的来源,证明了T3有能力差异调节BM成分的表达,并且可被视为甲状腺激素影响睾丸发育和分化的整合机制的一部分。

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