Macaque paneth cells express lymphoid chemokine CXCL13 and other antimicrobial peptides not previously described as

Carissa M Lucero1, Beth Fallert Junecko, Cynthia R Klamar

  • 1Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

Insights

CXCL13 chemokine expression in macaques shifts during simian immunodeficiency virus (SIV) infection, appearing in lymphoid follicles and unexpectedly in intestinal Paneth cells, impacting mucosal immunity and defense.

Area of Science:

  • Immunology
  • Mucosal Immunology
  • Infectious Disease

Background:

  • CXCL13 chemokine controls immune cell migration to lymphoid follicles.
  • CXCL13 mRNA levels increase in rhesus macaque spleen during AIDS.
  • Distinct localization patterns of CXCL13 mRNA and protein exist in germinal centers.

Purpose of the Study:

  • To examine CXCL13 levels and locations in cynomolgus macaque lymphoid and intestinal tissues.
  • To investigate shifts in CXCL13 expression during simian immunodeficiency virus (SIV) infection.
  • To explore Paneth cell expression of chemokines and antimicrobial peptides.

Main Methods:

  • In situ hybridization and protein localization techniques.
  • Analysis of lymphoid and intestinal tissues from cynomolgus macaques.
  • Examination of multiple chemokines and antimicrobial peptides (AMPs).

Main Results:

  • CXCL13 mRNA and protein localization patterns differ in germinal centers.
  • CXCL13 expression increases within and around follicles during SIV-induced AIDS.
  • CXCL13, β-defensin 2 (BDEF2), rhesus θ-defensin 1 (RTD-1), and Reg3γ are expressed by intestinal Paneth cells.
  • BDEF2 and RTD-1 expression by Paneth cells is newly reported.

Conclusions:

  • CXCL13 expression patterns change during SIV infection.
  • Paneth cells express CXCL13 and specific antimicrobial peptides, contributing to mucosal defense.
  • Findings enhance understanding of mucosal immunology, innate immunity, and host defense mechanisms.

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