2026-06-08T01:06:30Zhttps://docta.ucm.es/rest/oai/request
oai:docta.ucm.es:20.500.14352/1161532025-01-28T00:57:34Zcom_20.500.14352_14col_20.500.14352_15
Docta Complutense author Medraño Fernandez, Iria author Reyes Manzanas, Raquel author Olazabal, Isabel author Rodríguez, Elena author Sánchez Madrid, Francisco author Boussiotis, Vassiliki A. author Reche Gallardo, Pedro Antonio author Cabañas Gutiérrez, Carlos author Lafuente Duarte, María Esther 2025-01-27T08:37:05Z 2025-01-27T08:37:05Z 2013-02-19 Medraño-Fernandez, I., Reyes, R., Olazabal, I., Rodriguez, E., Sanchez-Madrid, F., Boussiotis, V. A., Reche, P. A., Cabañas, C., & Lafuente, E. M. (2013). RIAM (Rap1-interacting adaptor molecule) regulates complement-dependent phagocytosis. Cellular and molecular life sciences : CMLS, 70(13), 2395–2410. https://doi.org/10.1007/s00018-013-1268-6 1420-682X1420-9071 10.1007/s00018-013-1268-6 https://hdl.handle.net/20.500.14352/116153 https://doi.org/10.1007/s00018-013-1268-6 23420480 https://link.springer.com/article/10.1007/s00018-013-1268-6https://pubmed.ncbi.nlm.nih.gov/23420480/ Phagocytosis mediated by the complement receptor CR3 (also known as integrin αMß2 or Mac-1) is regulated by the recruitment of talin to the cytoplasmic tail of the ß2 integrin subunit. Talin recruitment to this integrin is dependent on Rap1 activation. However, the mechanism by which Rap1 regulates this event and CR3-dependent phagocytosis remains largely unknown. In the present work, we examined the role of the Rap1 effector RIAM, a talin-binding protein, in the regulation of complement-mediated phagocytosis. Using the human myeloid cell lines HL-60 and THP-1, we determined that knockdown of RIAM impaired αMß2 integrin affinity changes induced by stimuli fMLP and LPS. Phagocytosis of complement-opsonized RBC particles, but not of IgG-opsonized RBC particles, was impaired in RIAM knockdown cells. Rap1 activation via EPAC induced by 8-pCPT-2'-O-Me-cAMP resulted in an increase of complement-mediated phagocytosis that was abrogated by knockdown of RIAM in HL-60 and THP-1 cell lines and in macrophages derived from primary monocytes. Furthermore, recruitment of talin to ß2 integrin during complement-mediated phagocytosis was reduced in RIAM knockdown cells. These results indicate that RIAM is a critical component of the phagocytosis machinery downstream of Rap1 and mediates its function by recruiting talin to the phagocytic complement receptors. eng RIAM (Rap1-interacting adaptor molecule) regulates complement-dependent phagocytosis journal article 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URL https://docta.ucm.es/bitstreams/d4d0a869-9a01-4c43-b2e0-8ffe0775c4f8/download File MD5 0c8d83b43bb2fea2da80a591cf5e3a8f 1450907 application/pdf s00018-013-1268-6.pdf