Physiologic regulation of postovulatory neutrophil migration into vagina in mice by a C-X-C chemokine(s)

J Immunol. 1998 Jun 15;160(12):6159-65.

Abstract

Leukocytes, particularly neutrophils, infiltrate into female genital organs after ovulation in both humans and mice. In mice, a female sexual cycle consists of 5 phases: proestrus, estrus, metestrus-1, metestrus-2, and diestrus. Ovulation occurs at estrus; at metestrus-2, a large number of neutrophils infiltrate into the vaginal epithelium accompanied by an increased neutrophil number in vaginal lavage fluid. Concomitantly, concentrations of a functional IL-8 homologue, murine macrophage inflammatory protein (MIP)-2, were increased significantly in vaginal lavage fluid at metestrus-2 as compared with other phases. On the contrary, MIP-2 was not detected in plasma during the whole course of a sexual cycle. Moreover, immunohistochemical analyses demonstrated that MIP-2 protein expression was prominent at the upper layer of the vaginal epithelium at metestrus-2, in contrast to a marginal staining in the vaginal epithelium at proestrus and estrus. These results suggest that a C-X-C chemokine, MIP-2, was produced physiologically in the vaginal epithelium in a sexual cycle-dependent manner. Furthermore, the administration of neutralizing anti-IL-8R homologue Abs at proestrus abrogated leukocyte infiltration into the vagina at metestrus. However, anti-MIP-2 Abs reduced leukocyte influx at metestrus by approximately 50%. Thus, a murine IL-8 homologue, MIP-2, and its related molecules physiologically regulate neutrophil migration into the vagina in a sexual cycle-dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Chemokines, CXC / physiology*
  • Chemotactic Factors / immunology
  • Chemotaxis, Leukocyte*
  • Estrus / immunology
  • Female
  • Leukocyte Count
  • Mice
  • Mice, Inbred BALB C
  • Neutrophils / immunology*
  • Ovulation / immunology*
  • Rabbits
  • Receptors, Interleukin / metabolism
  • Receptors, Interleukin-8A
  • Vagina / immunology*

Substances

  • Antigens, CD
  • Chemokines, CXC
  • Chemotactic Factors
  • Receptors, Interleukin
  • Receptors, Interleukin-8A