Phenotypic and functional characterization of first-trimester human placental macrophages, Hofbauer cells

Jake Thomas(University of Cambridge), Anna Appios(University of Cambridge), Xiaohui Zhao(University of Cambridge), Roksana Dutkiewicz(University of Cambridge), Maria J. Donde(University of Cambridge), Colin Y.C. Lee(Agency for Science, Technology and Research), Praveena Naidu(University of Cambridge), Christopher Lee(Agency for Science, Technology and Research), Joana Cerveira(University of Cambridge), Bing Liu(Jinan University), Florent Ginhoux(Agency for Science, Technology and Research), Graham J. Burton(University of Cambridge), Russell S. Hamilton(University of Cambridge), Ashley Moffett(University of Cambridge), Andrew Sharkey(University of Cambridge), Naomi McGovern(University of Cambridge)
The Journal of Experimental Medicine
September 12, 2020
Cited by 191Open Access
Full Text

Abstract

Hofbauer cells (HBCs) are a population of macrophages found in high abundance within the stroma of the first-trimester human placenta. HBCs are the only fetal immune cell population within the stroma of healthy placenta. However, the functional properties of these cells are poorly described. Aligning with their predicted origin via primitive hematopoiesis, we find that HBCs are transcriptionally similar to yolk sac macrophages. Phenotypically, HBCs can be identified as HLA-DR-FOLR2+ macrophages. We identify a number of factors that HBCs secrete (including OPN and MMP-9) that could affect placental angiogenesis and remodeling. We determine that HBCs have the capacity to play a defensive role, where they are responsive to Toll-like receptor stimulation and are microbicidal. Finally, we also identify a population of placenta-associated maternal macrophages (PAMM1a) that adhere to the placental surface and express factors, such as fibronectin, that may aid in repair.


Related Papers

No related papers found

Powered by citation graph analysis