Expression of macrophage/dendritic cell–related molecules in lymph node sinus macrophages

Author:

Yamada Rin12ORCID,Ohnishi Koji3,Pan Cheng1,Yano Hiromu1,Fujiwara Yukio1ORCID,Shiota Takuya2,Mikami Yoshiki2,Komohara Yoshihiro1ORCID

Affiliation:

1. Department of Cell Pathology Graduate School of Medical Sciences Kumamoto Japan

2. Department of Diagnostic Pathology Kumamoto University Hospital Kumamoto Japan

3. Department of Pathology Aichi Medical University School of Medicine Nagakute Japan

Abstract

AbstractThe role of sinus macrophages (SMs) in anticancer immune responses has received considerable interest in recent years, but the types of molecules that are expressed in human SMs have not yet been clarified in detail. We therefore sought to identify dendritic cell (DC)– or macrophage‐related molecules in SMs in human lymph nodes (LNs). SMs are strongly positive for Iba‐1, CD163, CD169, and CD209. CD169 (clone SP216) reacted with almost all SMs, mainly in the cell surface membrane, while CD169 (clone HSn 7D2) reacted with a subpopulation of SMs, mainly in the cytoplasm, with a significant increase observed after IFN‐α stimulation. The immunoreactivity of clone HSn 7D2 was markedly reduced after transfection with small interfering RNA against CD169, while that of clone SP216 was slightly reduced. The induction of CCL8 and CXCL10 messenger RNA (mRNA) expression by IFN‐α was confirmed using cultured macrophages and RT‐qPCR, but fluorescence in situ hybridization did not detect CCL8 and CXCL10 mRNA expression in SMs. Single‐cell RNA sequence data of LNs indicated that the highest level of CXCL10 gene expression occurred in monocytes. In conclusion, we found that CD209, also known as DC‐related molecule, was expressed in human SMs. The heterogeneity observed in CD169 reacted with cone HSn 7D2 and SP216 was potentially due to the modification of CD169 protein by IFN stimulation. Further, no expression of CXCL10 mRNA in SMs suggested that SMs might be resident macrophages.

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

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