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Updated: May 10, 2026

Isolation and Characterization of Dendritic Cells and Macrophages from the Mouse Intestine
Published on: May 21, 2012
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.
Abstract:
CXCL13 is a constitutively expressed chemokine that controls migration of immune cells to lymphoid follicles. Previously, we found CXCL13 mRNA levels increased in rhesus macaque spleen tissues during AIDS. This led us to examine the levels and locations of CXCL13 by detailed in situ methods in cynomolgus macaque lymphoid and intestinal tissues. Our results revealed that there were distinct localization patterns of CXCL13 mRNA compared to protein in germinal centers. These patterns shifted during the course of simian immunodeficiency virus (SIV) infection, with increased mRNA expression within and around follicles during AIDS compared to uninfected or acutely infected animals. Unexpectedly, CXCL13 expression was also found in abundance in Paneth cells in crypts throughout the small intestine. Therefore, we expanded our analyses to include chemokines and antimicrobial peptides (AMPs) not previously demonstrated to be expressed by Paneth cells in intestinal tissues. We examined the expression patterns of multiple chemokines, including CCL25, as well as α-defensin 6 (DEFA6), β-defensin 2 (BDEF2), rhesus θ-defensin 1 (RTD-1), and Reg3γ in situ in intestinal tissues. Of the 10 chemokines examined, CXCL13 was unique in its expression by Paneth cells. BDEF2, RTD-1, and Reg3γ were also expressed by Paneth cells. BDEF2 and RTD-1 previously have not been shown to be expressed by Paneth cells. These findings expand our understanding of mucosal immunology, innate antimicrobial defenses, homeostatic chemokine function, and host protective mechanisms against microbial translocation.
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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