Inhibition of CD36-dependent phagocytosis by prostaglandin E2 contributes to the development of endometriosis

Pei‐Chin Chuang, Pei-Chin Chuang, Chuang PC, Yiu-Juian Lin, Lin YJ, Meng‐Hsing Wu, Meng-Hsing Wu, Wu MH, Lih-Yuh C. Wing, Wing LY, Yutaka Shoji, Shoji Y, Shaw‐Jenq Tsai, Shaw-Jenq Tsai
The American Journal of Pathology · 2009 · vol. 176(2) , pp. 850–860 · doi:10.2353/ajpath.2010.090551 · PMID:20035060 · PMC2808090 · W1982670199
Lab / animal OA: bronze CC0 ⤵ 74 in-corpus citations
📄 Open PDF View on OpenAlex View on PubMed View at publisher
⚙ AI-generated summary by gemini-2.5-flash-lite, 2026-06-08 ⓘ

Prostaglandin E2 inhibits CD36-dependent phagocytosis, a process that contributes to the development of endometriosis.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

Abstract

Dysfunction in macrophage-mediated phagocytosis of aberrant cells that undergo retrograde transport to the peritoneal cavity is considered an important factor in the development of endometriosis. However, the mechanisms responsible for the loss of function of macrophages remain largely unknown. Herein, we report that prostaglandin (PG) E(2), via the EP2 receptor-dependent signaling pathway, inhibits the expression of CD36 in peritoneal macrophages, resulting in reduced phagocytic ability. PGE(2)-mediated inhibition of macrophage phagocytic capability was restored by ectopic expression of CD36. Treatment with PGE(2) inhibited CD36-dependent phagocytosis of peritoneal macrophages and increased the number and size of endometriotic lesions in mice. In contrast, blockade of PGE(2) production by cyclooxygenase inhibitors enhanced the phagocytic ability of peritoneal macrophages and reduced endometriotic lesion formation. Taken together, our findings reveal a potential mechanism of immune dysfunction during endometriosis development and may contribute to the design of an effective prevention/treatment regimen.

My notes (saved in your browser only)

Condition tags

endometriosis

MeSH descriptors

CD36 Antigens Dinoprostone Endometriosis Peritoneal Diseases Phagocytosis Phagocytosis Phagocytosis Phagocytosis Phagocytosis Animals Animals CD36 Antigens CD36 Antigens CD36 Antigens CD36 Antigens Cells, Cultured Cells, Cultured Dinoprostone Dinoprostone Dinoprostone

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (48)

Cited by (50)

Source provenance

europepmc
last seen: 2026-10-10T06:11:15.153948+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-10-08T21:07:11.085580+00:00
License: CC0 · commercial use OK