[Influence of FasL overexpression in transgenic mice on the immune regulative function of Sertoli cell]

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2004 Jul;20(4):456-60.
[Article in Chinese]

Abstract

Aim: To study the influence of FasL overexpression in transgenic mice on the Sertoli cell immune response to testicular infection.

Methods: Ureaplasma urealyticum (UU) was directly injected into bladders of FasL transgenic mice and wild-type mice respectively, to mimic an ascending infection pathway. At week 1, 2 and 3 after injection, respectively, the mice were put to death to observe the pathological alterations in testis section. And at the same time the differences of FasL, TGF-beta, IL-1alpha and IL-6 expressions on Sertoli cells were compared by immunohistochemical staining between wild mice and transgenic mice before and after infection, respectively. The high-purified Sertoli cells were isolated from the testis tissue of wild-type mice, comparing apoptotic capability of Fas(+) Jurkat cells mediated by FasL(+) Sertoli cells of wild control and wild UU-infected groups.

Results: The pathological changes of testis tissue from transgenic mice were more serious as compared with wild-type mice and the model of cytokines secreted by sertoli cells was distinctive between the two kinds of mice. The UU-infected Sertoli cells increased Fas(+) Jurkat cell apoptosis.

Conclusion: FasL overexpression can influence the cytokine's secretion in the process of anti-infection immunity and further affects the immune balance of testis locality. Not all FasL over expression is benefit to body's anti-infection immune response.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cytokines / metabolism*
  • Fas Ligand Protein
  • Humans
  • Interleukin-1 / metabolism
  • Interleukin-6 / metabolism
  • Jurkat Cells / pathology
  • Male
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Transgenic
  • Sertoli Cells / metabolism*
  • Testicular Diseases / metabolism
  • Testicular Diseases / microbiology
  • Testicular Diseases / pathology*
  • Transforming Growth Factor beta / metabolism
  • Ureaplasma Infections / metabolism
  • Ureaplasma Infections / pathology*
  • Ureaplasma urealyticum

Substances

  • Cytokines
  • FASLG protein, human
  • Fas Ligand Protein
  • Fasl protein, mouse
  • Interleukin-1
  • Interleukin-6
  • Membrane Glycoproteins
  • Transforming Growth Factor beta