The scavenger receptor SR-A I/II (CD204) signals via the receptor tyrosine kinase Mertk during apoptotic cell uptake by murine macrophages

• Published in: Journal of leukocyte biology Vol. 84; no. 2; pp. 510 - 518
• Main Authors: Todt, Jill C., Hu, Bin, Curtis, Jeffrey L.
• Format: Journal Article
• Language: English
• Published: United States Society for Leukocyte Biology 01-08-2008; The Society for Leukocyte Biology
• Subjects: Animals; apoptosis; Apoptosis - physiology; c-Mer Tyrosine Kinase; inbred strains; Inflammation - physiopathology; Macrophages - physiology; Mice; Mice, Knockout; phagocytosis; protein kinases/phosphatases; Proto-Oncogene Proteins - physiology; Receptor Protein-Tyrosine Kinases - physiology; Receptors, Signal Transduction, and Genes; Scavenger Receptors, Class A - deficiency; Scavenger Receptors, Class A - genetics; Scavenger Receptors, Class A - physiology; signal transduction; T-Lymphocytes - physiology
• ISSN: 0741-5400; 1938-3673
• DOI: 10.1189/jlb.0307135

Apoptotic cells (AC) must be cleared by macrophages (Mø) to resolve inflammation effectively. Mertk and scavenger receptor A (SR‐A) are two of many receptors involved in AC clearance. As SR‐A lacks enzymatic activity or evident intracellular signaling motifs, yet seems to signal in some cell types, we hypothesized that SR‐A signals via Mer receptor tyrosine kinase (Mertk), which contains a multisubstrate docking site. We induced apoptosis in murine thymocytes by dexamethasone and used Western blotting and immunoprecipitation to analyze the interaction of Mertk and SR‐A in the J774A.1 (J774) murine Mø cell line and in peritoneal Mø of wild‐type mice and SR‐A−/− mice. Phagocytosis (but not adhesion) of AC by J774 was inhibited by anti‐SR‐A or function‐blocking SR‐A ligands. In resting J774, SR‐A was associated minimally with unphosphorylated (monomeric) Mertk; exposure to AC induced a time‐dependent increase in association of SR‐A with Mertk in a direct or indirect manner. Anti‐SR‐A inhibited AC‐induced phosphorylation of Mertk and of phospholipase Cγ2, essential steps in AC ingestion. Relative to tissue Mø of wild‐type mice, AC‐induced Mertk phosphorylation was reduced and delayed in tissue Mø of SR‐A−/− mice, as was in vitro AC ingestion at early time‐points. Thus, during AC uptake by murine Mø, SR‐A is essential for optimal phosphorylation of Mertk and subsequent signaling required for AC ingestion. These data support the Mertk/SR‐A complex as a potential target to manipulate AC clearance and hence, resolution of inflammation and infections.