Perryman K J, Stanton P G, Loveland K L, McLachlan R I, Robertson D M
Prince Henry's Institute of Medical Research, Monash Medical Center, Clayton, Victoria, Australia.
Endocrinology. 1996 Sep;137(9):3877-83. doi: 10.1210/endo.137.9.8756560.
The procession of round spermatids through stages VII and VIII of the rat spermatogenic cycle is critically dependent on testosterone (T). When intratesticular T levels are reduced, round spermatids appear to slough from the seminiferous epithelium, resulting in the disappearance of elongated spermatids. We hypothesized that T-dependent cell adhesion molecules are involved in Sertoli cell-round spermatid interactions. This study examined the hormonal regulation of one candidate cell adhesion molecule, N-cadherin, in vitro and its participation in Sertoli cell-round spermatid adhesion in coculture. Sertoli cells were isolated from 20-day-old Sprague-Dawley rats; treated with FSH and T, alone or in combination; and incubated for 48 h before determination of N-cadherin concentrations in Sertoli cell extracts by RIA. Both FSH and T significantly increased the cellular content of N-cadherin (3.7-fold), whereas FSH or T alone had no effect. Round spermatids were isolated from adult rats, and their adhesion to Sertoli cells was assessed in a 48-h coculture in the presence of FSH, T, or FSH plus T. Adherent round spermatids were quantitated by histological evaluation after staining with the periodic acid-Schiff reaction. A dose-dependent increase in round spermatid density (number of round spermatids bound per 10,000-microns2 Sertoli cell culture surface area) was observed with increasing T doses (7-28 ng/ml) in the presence of FSH (1 microgram/ml), whereas FSH and T alone at these doses produced no effect. T also increased the N-cadherin content of the cocultures in a dose-dependent manner in the presence of FSH. Addition of an N-cadherin antiserum to the Sertoli cell-round spermatid coculture in the presence of FSH and T significantly (P < 0.0001) reduced round spermatid density by 65%. It is concluded that both the production of N-cadherin by Sertoli cells and the binding of round spermatids to Sertoli cells are stimulated in a synergistic manner by T and FSH. Furthermore, the immunoneutralization data suggest the active involvement of N-cadherin in round spermatid-Sertoli cell adhesion in vitro. N-Cadherin may be one of the factors that subserve the androgen-dependent process of round to elongated spermatid maturation.
圆形精子细胞在大鼠生精周期的Ⅶ期和Ⅷ期的进程严重依赖于睾酮(T)。当睾丸内T水平降低时,圆形精子细胞似乎从生精上皮脱落,导致长形精子细胞消失。我们推测T依赖性细胞黏附分子参与支持细胞与圆形精子细胞的相互作用。本研究检测了一种候选细胞黏附分子N-钙黏蛋白在体外的激素调节及其在共培养中参与支持细胞与圆形精子细胞黏附的情况。从20日龄的Sprague-Dawley大鼠分离支持细胞;单独或联合用促卵泡激素(FSH)和T处理;孵育48小时后,通过放射免疫分析法测定支持细胞提取物中N-钙黏蛋白的浓度。FSH和T均显著增加N-钙黏蛋白的细胞含量(3.7倍),而单独使用FSH或T则无作用。从成年大鼠分离圆形精子细胞,并在存在FSH、T或FSH加T的情况下进行48小时共培养,评估其与支持细胞的黏附。在用过碘酸-希夫反应染色后,通过组织学评估对黏附的圆形精子细胞进行定量。在存在FSH(1微克/毫升)的情况下,随着T剂量(7 - 28纳克/毫升)增加,观察到圆形精子细胞密度呈剂量依赖性增加(每10000平方微米支持细胞培养表面积结合的圆形精子细胞数量),而单独使用这些剂量的FSH和T则无作用。在存在FSH的情况下,T也以剂量依赖性方式增加共培养物中N-钙黏蛋白的含量。在存在FSH和T时,向支持细胞 - 圆形精子细胞共培养物中加入N-钙黏蛋白抗血清显著(P < 0.0001)使圆形精子细胞密度降低了65%。得出的结论是,支持细胞产生N-钙黏蛋白以及圆形精子细胞与支持细胞的结合均受到T和FSH的协同刺激。此外,免疫中和数据表明N-钙黏蛋白在体外积极参与圆形精子细胞与支持细胞的黏附。N-钙黏蛋白可能是有助于圆形精子细胞向长形精子细胞成熟的雄激素依赖性过程的因素之一。