Nitric oxide production of rat Leydig and Sertoli cells is stimulated by round spermatid factor(s)

Mol Cell Endocrinol. 2000 Feb 25;160(1-2):99-105. doi: 10.1016/s0303-7207(99)00257-9.

Abstract

In this study, we provide evidence of cell-to-cell interaction between rat germ cells and Leydig or Sertoli cells in relation to nitric oxide (NO) production and inducible nitric oxide synthase (iNOS) messenger RNA (mRNA) expression. As a result of being cultured in a round spermatid-conditioned medium (RSd-CM), NO production in both Leydig and Sertoli cells increased in proportion to the length of the culture period. iNOS mRNA expression in both types of cells also increased in a dose-dependent manner as a result of being cultured with RSd-CM. This increase was detected as early as 3 h and was maintained up to 24 h. In contrast, neither NO production nor iNOS mRNA increased in either type of cell following culture in a pachytene spermatocyte-conditioned medium (PS-CM). Our findings suggest that RSd may control NO production of Leydig and Sertoli cells. This cell-to-cell interaction may be an important mechanism of regulation of testicular function.

MeSH terms

  • Animals
  • Cell Communication
  • Culture Media, Conditioned
  • Cytokines / pharmacology
  • Hormones / pharmacology
  • In Vitro Techniques
  • Kinetics
  • Leydig Cells / metabolism*
  • Male
  • Nitric Oxide / biosynthesis*
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase Type II
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sertoli Cells / drug effects
  • Sertoli Cells / metabolism*
  • Spermatids / cytology
  • Spermatids / metabolism*

Substances

  • Culture Media, Conditioned
  • Cytokines
  • Hormones
  • RNA, Messenger
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat