Vincent S, Segretain D, Nishikawa S, Nishikawa S I, Sage J, Cuzin F, Rassoulzadegan M
Unité 470 de l'INSERM, Faculté des Sciences, Université de Nice, France.
Development. 1998 Nov;125(22):4585-93. doi: 10.1242/dev.125.22.4585.
The Kit receptor and its ligand KL, which together constitute an essential effector at various stages of embryonic development, are both present during adult gametogenesis. In the testis, KL is expressed in Sertoli cells, and Kit in germ cells, starting at the premeiotic stages. A series of observations indicated previously a role in spermatogonia survival, without excluding a possible function at later stages. We identified a complex pattern of expression of the two components in the adult murine testis, suggestive of a role in the meiotic progression of spermatocytes. At stages VII-VIII of the cycle of the seminiferous epithelium, the time when spermatocytes enter meiosis, the membrane-associated form of KL extends on the Sertoli cell from the peripheral to the adluminal compartment of the tubule. We also found that the receptor is present on the surface of germ cells up to the pachytene stage. The availability of differentiated Sertoli cell lines, which express the KL protein and support part of the maturation of germ cells in coculture, allowed us to ask whether, in the in vitro reconstructed system, transit of spermatocytes through meiosis requires the Kit-KL interaction. Addition of a blocking monoclonal antibody against the Kit receptor (ACK2) inhibited extensively the appearance of haploid cells and the expression of a haploid-phase-specific gene (Prm1). Recognition of the supporting Sertoli cell by germ cells was not affected, indicating a requirement for the activity of the receptor for either entering or completing meiosis. Involvement of the membrane-associated form of the ligand was suggested by the observation that addition of the soluble form of KL was equally inhibitory.
Kit受体及其配体KL在胚胎发育的各个阶段共同构成一种重要的效应因子,在成年配子发生过程中也均有表达。在睾丸中,从减数分裂前阶段开始,KL在支持细胞中表达,而Kit在生殖细胞中表达。此前一系列观察表明其在精原细胞存活中起作用,但并未排除在后期阶段可能具有的功能。我们在成年小鼠睾丸中鉴定出这两种成分的复杂表达模式,提示其在精母细胞减数分裂进程中发挥作用。在生精上皮周期的VII - VIII阶段,即精母细胞进入减数分裂的时期,膜结合形式的KL在支持细胞上从生精小管的外周向管腔侧延伸。我们还发现该受体在粗线期之前的生殖细胞表面均有存在。可分化的支持细胞系能够表达KL蛋白并在共培养中支持部分生殖细胞的成熟,这使我们能够探究在体外重建系统中,精母细胞通过减数分裂是否需要Kit - KL相互作用。添加针对Kit受体的阻断单克隆抗体(ACK2)可广泛抑制单倍体细胞的出现以及单倍体阶段特异性基因(Prm1)的表达。生殖细胞对支持性支持细胞的识别不受影响,这表明进入或完成减数分裂需要该受体的活性。添加可溶性形式的KL同样具有抑制作用,这表明配体的膜结合形式也参与其中。