Piquet-Pellorce C, Dorval I, Jégou B
Groupe d'étude de la Reproduction chez le Mâle, INSERM U 435, Université de Rennes I.
Contracept Fertil Sex. 1997 Jul-Aug;25(7-8):565-8.
Correct regulation of spermatogonial mitosis and, more specifically, the control of the balance between differentiation and proliferation to allow renewal of the stem cell stock, are essential for the maintenance of spermatozoa production throughout life. The mechanisms underlying this control are still unknown. However, recent studies suggest that some locally produced cytokines may be involved in the regulation of spermatogonial activity. In this context, Leukemia Inhibitory Factor (LIF) exhibits interesting properties regarding stem cells and, particularly, primordial germ cells. The present study aimed at investigating LIF production and LIF binding abilities by/of the different testicular cells types (somatic and germ cells). Our study demonstrates that LIF is produced within the testis, mainly by peritubular cells which are in the vicinity of spermatogonia, the latter cells expressing high levels of LIF receptors. These results strongly suggest an involvement of LIF in the control of spermatogonial activity.
精原细胞有丝分裂的正确调控,更具体地说,控制分化与增殖之间的平衡以维持干细胞储备的更新,对于一生之中精子生成的维持至关重要。这种调控背后的机制仍然未知。然而,最近的研究表明,一些局部产生的细胞因子可能参与精原细胞活性的调控。在此背景下,白血病抑制因子(LIF)在干细胞尤其是原始生殖细胞方面表现出有趣的特性。本研究旨在调查不同睾丸细胞类型(体细胞和生殖细胞)产生LIF的情况以及它们与LIF的结合能力。我们的研究表明,LIF在睾丸内产生,主要由精原细胞附近的睾丸周细胞产生,而精原细胞表达高水平的LIF受体。这些结果有力地表明LIF参与了精原细胞活性的调控。