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脾巨噬细胞可改变睾丸间质细胞的类固醇生成。

Splenic macrophages can modify steroidogenesis of Leydig cells.

作者信息

Onami S, Matsuyama S, Nishihara M, Takahashi M

机构信息

Department of Veterinary Physiology, Veterinary Medical Science, University of Tokyo, Japan.

出版信息

Endocr J. 1996 Oct;43(5):477-85. doi: 10.1507/endocrj.43.477.

Abstract

A large amount of LH/hCG treatment given to male rats is known to suppress the enzyme activity of cytochrome P450c17 in Leydig cells for 48 h. A high dose LH/hCG injection is also known to allow immunocytes, such as macrophages, to migrate into the testicular interstitial compartment. It has not been known, however, whether these cells play a role in that suppression. In this study, we examined if splenic macrophages have any effects on testosterone secretion from Leydig cells by culturing rat testicular interstitial cells (TIC). Splenic macrophages co-cultured with TIC significantly suppressed testosterone secretion. Macrophages co-cultured reduced both progesterone to testosterone conversion and the amount of cytochrome P450c17 mRNA. The conditioned medium (SMCM), prepared by culturing macrophages for 12 h, significantly reduced either testosterone secretion from TIC or progesterone to testosterone conversion by TIC. These results indicate that splenic macrophages suppress testosterone secretion from Leydig cells by suppressing the cytochrome P450c17 enzyme in vitro, and that this effect is mediated at least in part by some soluble factors secreted from macrophages. Splenic macrophages migrating into the testis after LH/hCG stimulation could play a role in suppressing cytochrome P450c17 in Leydig cells.

摘要

已知给雄性大鼠大量注射促黄体生成素/人绒毛膜促性腺激素(LH/hCG)会抑制睾丸间质细胞中细胞色素P450c17的酶活性达48小时。还已知高剂量注射LH/hCG会使免疫细胞,如巨噬细胞,迁移至睾丸间质区。然而,尚不清楚这些细胞在这种抑制作用中是否发挥作用。在本研究中,我们通过培养大鼠睾丸间质细胞(TIC)来检测脾巨噬细胞是否对睾丸间质细胞的睾酮分泌有任何影响。与TIC共培养的脾巨噬细胞显著抑制了睾酮分泌。共培养的巨噬细胞降低了孕酮向睾酮的转化以及细胞色素P450c17 mRNA的量。通过培养巨噬细胞12小时制备的条件培养基(SMCM)显著降低了TIC的睾酮分泌或TIC的孕酮向睾酮的转化。这些结果表明,脾巨噬细胞在体外通过抑制细胞色素P450c17酶来抑制睾丸间质细胞的睾酮分泌,并且这种作用至少部分是由巨噬细胞分泌的一些可溶性因子介导的。LH/hCG刺激后迁移至睾丸的脾巨噬细胞可能在抑制睾丸间质细胞中的细胞色素P450c17方面发挥作用。

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