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普通狨猴和人类睾丸中趋化因子CXCL11、CXCL12及其受体CXCR7的发育表达模式

Developmental expression patterns of chemokines CXCL11, CXCL12 and their receptor CXCR7 in testes of common marmoset and human.

作者信息

Westernströer Birgit, Langenstroth Daniel, Kliesch Sabine, Troppmann Britta, Redmann Klaus, Macdonald Joni, Mitchell Rod, Wistuba Joachim, Schlatt Stefan, Neuhaus Nina

机构信息

Centre of Reproductive Medicine and Andrology, CeRA, Institute of Reproductive and Regenerative Biology, Albert-Schweizer-Campus 1, Building D11, 48149, Münster, Germany.

出版信息

Cell Tissue Res. 2015 Sep;361(3):885-98. doi: 10.1007/s00441-015-2164-1. Epub 2015 Mar 26.

Abstract

The chemokine receptor CXCR7 interacts with the chemokines CXCL11 and CXCL12. During development, this ligand receptor system (C-X-C) provokes cell-type-specific responses in terms of migration, adhesion or ligand sequestration. It is active in zebrafish and rodents but no data are available for its presence or function in primate testes. Real-time quantitative polymerase chain reaction was performed in monkeys to detect CXCL11, CXCL12 and CXCR7. At the protein level, CXCL12 and CXCR7 were localized in the testes of the marmoset (Callitrix jacchus) whereas CXCR7 patterns were determined for various stages in human testes. Morphometry and flow cytometry were applied to quantify CXCR7-positive cells in monkeys. Transcript levels and protein expression of CXCR7 were detectable throughout testicular development. In both species, CXCR7 protein expression was restricted to premeiotic germ cells. In immature marmoset testes, 69.9% ± 9% of the total germ cell population were labelled for CXCR7, whereas in the adult, 4.7% ± 2.7% were positive for CXCR7. CXCL12 mRNA was detectable in all developmental stages in marmosets. The CXCL12 protein was exclusively localized to Sertoli cells. This pattern of CXCL12/CXCR7 indicates their involvement in regulatory processes that possibly orchestrate the interaction between undifferentiated germ cells and Sertoli cells.

摘要

趋化因子受体CXCR7与趋化因子CXCL11和CXCL12相互作用。在发育过程中,这种配体受体系统(C-X-C)在细胞迁移、黏附或配体隔离方面引发细胞类型特异性反应。它在斑马鱼和啮齿动物中具有活性,但尚无关于其在灵长类动物睾丸中的存在或功能的数据。对猴子进行实时定量聚合酶链反应以检测CXCL11、CXCL12和CXCR7。在蛋白质水平上,CXCL12和CXCR7定位于狨猴(Callitrix jacchus)的睾丸中,而在人类睾丸的不同阶段确定了CXCR7模式。应用形态学测量和流式细胞术对猴子体内CXCR7阳性细胞进行定量。在整个睾丸发育过程中均可检测到CXCR7的转录水平和蛋白质表达。在这两个物种中,CXCR7蛋白表达均局限于减数分裂前的生殖细胞。在未成熟的狨猴睾丸中,69.9%±9%的总生殖细胞群体被标记为CXCR7,而在成年狨猴中,4.7%±2.7%为CXCR7阳性。在狨猴的所有发育阶段均可检测到CXCL12 mRNA。CXCL12蛋白仅定位于支持细胞。CXCL12/CXCR7的这种模式表明它们参与了可能协调未分化生殖细胞与支持细胞之间相互作用的调节过程。

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