Expression of toll-like receptors and their regulatory roles in murine cardiac telocytes

J Cell Mol Med. 2019 Aug;23(8):5360-5368. doi: 10.1111/jcmm.14416. Epub 2019 Jun 24.

Abstract

Telocytes, newly discovered in the last decade, are interstitial cells found in numerous organs, with multiple proposed potential biological functions. Toll-like receptors (TLRs) play an important role in innate and adaptive immunity by recognizing pathogen-associated molecular patterns (PAMPs). However, it is still unknown whether telocytes express these innate receptors. We sought to determine the expression and role of TLRs in telocytes. In our study, we primarily detected TLR1-9 expression in telocytes. The proliferation, apoptosis and immunoregulatory activity of telocytes activated with or without TLR ligands were determined. Our results showed that purified telocytes expressed TLR2, TLR3 and TLR5. In particular, telocytes expressed high levels of TLR2 as observed using flow cytometry. When we stimulated telocytes with TLR2 or TLR3 agonists (Pam3CSK4, PolyI:C), iNOS expression was greatly increased after Pam3CSK4 treatment. Additionally, telocyte proliferation was reduced and cell apoptosis was increased after TLR agonist stimulation. A co-culture experiment showed that supernatant from telocytes pretreated with Pam3CSK4 inhibited T cell activation much more than that from untreated telocytes and this effect was mediated by iNOS. Overall, our results demonstrated TLR expression on telocytes for the first time and provided evidence of an immunoregulatory role of telocytes, indicating their clinical potential.

Keywords: immunosuppression; secretory profile; telocytes; toll-like receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cell Proliferation / physiology
  • Cells, Cultured
  • Flow Cytometry / methods
  • Ligands
  • Lymphocyte Activation / physiology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • T-Lymphocytes / metabolism
  • Telocytes / metabolism*
  • Toll-Like Receptors / metabolism*

Substances

  • Ligands
  • Toll-Like Receptors