Toll-like receptor expression and function in the COV434 granulosa cell line

Am J Reprod Immunol. 2012 Sep;68(3):205-17. doi: 10.1111/j.1600-0897.2011.01103.x. Epub 2012 Jan 11.

Abstract

Problem: Bacterial infections perturb ovarian follicle function, despite the lack of immune cells such as macrophages within healthy ovarian follicles. This study examined whether the granulosa cells that line ovarian follicles could, like macrophages, use Toll-like receptors (TLRs) to detect pathogen-associated molecular patterns (PAMPs) and initiate inflammation.

Method of study: The COV434 human granulosa and THP-1 macrophage cell lines were used to determine the expression of TLRs and measure the production of cytokines, chemokines and estradiol in response to the PAMPs lipopolysaccharide, peptidoglycan, lipoteichoic acid and flagellin from bacteria.

Results: The THP-1 and granulosa cells expressed mRNA for TLR1-10 and TLR4-10, respectively. The supernatants of THP-1 cells accumulated IL-1β, IL-6, IL-8 and CCL5 in response to PAMPs. Treatment of granulosa cells with PAMPs increased expression of IL1B mRNA after 3 hr, but did not change the accumulation of IL-1β, IL-6, IL-8, CCL5 or estradiol. Granulosa cells produced IL-8 constitutively, and this was reduced using chemical inhibitors for p38 and JNK mitogen-activated protein kinases.

Conclusion: The COV434 human granulosa cell line expresses TLRs and constitutively secretes IL-8 but only mounts an inflammatory response to PAMPs at the transcriptional level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Culture Media
  • Cytokines / biosynthesis
  • Cytokines / immunology
  • Cytokines / metabolism
  • Estradiol / biosynthesis
  • Estradiol / immunology
  • Female
  • Flagellin / pharmacology
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology
  • Granulosa Cells / drug effects
  • Granulosa Cells / immunology
  • Granulosa Cells / metabolism*
  • Humans
  • Lipopolysaccharides / pharmacology
  • MAP Kinase Kinase 4 / antagonists & inhibitors
  • MAP Kinase Kinase 4 / metabolism
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism
  • Peptidoglycan / pharmacology
  • Protein Isoforms / genetics
  • Protein Isoforms / immunology
  • Protein Kinase Inhibitors / pharmacology
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / immunology
  • Teichoic Acids / pharmacology
  • Toll-Like Receptors / genetics*
  • Toll-Like Receptors / immunology
  • Transcription, Genetic / drug effects*
  • Transcription, Genetic / immunology
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Culture Media
  • Cytokines
  • Lipopolysaccharides
  • Peptidoglycan
  • Protein Isoforms
  • Protein Kinase Inhibitors
  • RNA, Messenger
  • Teichoic Acids
  • Toll-Like Receptors
  • Flagellin
  • Estradiol
  • lipoteichoic acid
  • p38 Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4