bfc, a novel serpent co-factor for the expression of croquemort, regulates efferocytosis in Drosophila melanogaster
Open accessAbstract
Efferocytosis is the process by which phagocytes recognize, engulf, and digest (or clear) apoptotic cells during development. Impaired efferocytosis is associated with developmental defects and autoimmune diseases. In Drosophila melanogaster, recognition of apoptotic cells requires phagocyte surface receptors, including the scavenger receptor CD36-related protein, Croquemort (Crq, encoded by crq). In fact, Crq expression is upregulated in the presence of apoptotic cells, as well as in response to excessive apoptosis. Here, we identified a novel gene bfc(booster for croquemort), which plays a role in efferocytosis, specifically the regulation of the crq expression. We found that Bfc protein interacts with the zinc finger domain of the GATA transcription factor Serpent (Srp), to enhance its direct binding to the crq promoter; thus, they function together in regulating crq expression and efferocytosis. Overall, we show that Bfc serves as a Srp co-factor to upregulate the transcription of the crq encoded receptor, and consequently boosts macrophage efferocytosis in response to excessive apoptosis. Therefore, this study clarifies how phagocytes integrate apoptotic cell signals to mediate efferocytosis.
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Efferocytosis is a critical physiological process through which macrophages recognize and engulf apoptotic cells to maintain tissue homeostasis.
“Efferocytosis is a critical physiological process through which macrophages recognize and engulf ACs to maintain tissue homeostasis.18,19,20”
From Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer (2026) · cites this paper as [20]
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Clearance of apoptotic corpses
Fullard, J. F., Kale, A., & Baker, N. E. (2009) · Apoptosis · doi:10.1007/s10495-009-0335-9 · Cited by 46 · see citing works
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Xi, Y., Zhao, Z., Zhou, Y., Yin, C., Li, Y., Xu, X., Jin, W., Lin, C., Zhao, K., Kuang, J., et al. (2026) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102529 · Cited by 12 · see citing works
“20 Within the TME, efferocytosis aids in clearing dead cells and modulates immune responses by secreting anti-inflammatory cytokines.”
- Authors
- Zheng, Q., Gao, N., Sun, Q., Li, X., Wang, Y., & Xiao, H.
- Affiliations
- Shaanxi Normal University (CN)
- Corresponding author
- Xiao, Hui
- Venue
- PLOS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2021-12-03
- Volume
- 17
- Issue
- 12
- Pages
- e1009947
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC8673676
- OpenAlex
- W3216813228
- Cited by
- 12
- References
- 1
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 2
- FWCI
- 0.56
- Type
- journal article
- Language
- en
- Update notices
- new_version (2021-12-15)
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation Key Project (breeding program) of China (91954114)
- National Natural Science Foundation of China (31671439)
- National Natural Science Foundation of China Youth Program (31801164)
- the program of Innovative Research Team for the Central Universities of Shaanxi Normal University (GK202001004)
- the Fundamental Research Key Project Funds for the Central Universities of Shaanxi Normal University (GK202007009)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Immunology and Microbiology › Immunology › Invertebrate Immune Response Mechanisms
- Keywords
- efferocytosis, serpents, GATA transcription factors, transcriptional cofactors, macrophages, Drosophila melanogaster
- MeSH terms
- Animals, Drosophila melanogaster, Macrophages, Phagocytes, Phagocytosis, Receptors, Cell Surface, Apoptosis, Gene Expression Regulation, Developmental, CD36 Antigens, Drosophila Proteins, GATA Transcription Factors, Receptors, Scavenger
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