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Resolvin D2-G-Protein Coupled Receptor 18 Enhances Bone Marrow Function and Limits Steatosis and Hepatic Collagen Accumulation in Aging.
Fitzgerald, Hannah; Bonin, Jesse L; Khan, Sayeed; Eid, Maya; Sadhu, Sudeshna; Rahtes, Allison; Lipscomb, Masharh; Biswas, Nirupam; Decker, Christa; Nabage, Melisande; Ramos, Ramon Bossardi; Duarte, Giesse Albeche; Marinello, Michael; Chen, Anne; Aydin, Hasan Basri; Mena, Hebe Agustina; Gilliard, Kurrim; Spite, Matthew; DiPersio, C Michael; Adam, Alejandro P; MacNamara, Katherine C; Fredman, Gabrielle.
  • Fitzgerald H; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Bonin JL; The Department of Immunology and Microbial Disease, Albany Medical College, Albany, New York.
  • Khan S; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Eid M; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Sadhu S; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Rahtes A; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Lipscomb M; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Biswas N; The Department of Immunology and Microbial Disease, Albany Medical College, Albany, New York.
  • Decker C; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Nabage M; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Ramos RB; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Duarte GA; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Marinello M; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Chen A; Department of Pathology, Albany Medical College, Albany, New York.
  • Aydin HB; Department of Pathology, Albany Medical College, Albany, New York.
  • Mena HA; Department of Anesthesiology, Perioperative and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Gilliard K; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • Spite M; Department of Anesthesiology, Perioperative and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
  • DiPersio CM; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York; Department of Surgery, Albany Medical College, Albany, New York.
  • Adam AP; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York.
  • MacNamara KC; The Department of Immunology and Microbial Disease, Albany Medical College, Albany, New York. Electronic address: macnamk@amc.edu.
  • Fredman G; The Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York. Electronic address: fredmag@amc.edu.
Am J Pathol ; 193(12): 1953-1968, 2023 12.
Article en En | MEDLINE | ID: mdl-37717941
Aging is associated with nonresolving inflammation and tissue dysfunction. Resolvin D2 (RvD2) is a proresolving ligand that acts through the G-protein-coupled receptor called GPR18. Unbiased RNA sequencing revealed increased Gpr18 expression in macrophages from old mice, and in livers from elderly humans, which was associated with increased steatosis and fibrosis in middle-aged (MA) and old mice. MA mice that lacked GPR18 on myeloid cells had exacerbated steatosis and hepatic fibrosis, which was associated with a decline in Mac2+ macrophages. Treatment of MA mice with RvD2 reduced steatosis and decreased hepatic fibrosis, correlating with increased Mac2+ macrophages, increased monocyte-derived macrophages, and elevated numbers of monocytes in the liver, blood, and bone marrow. RvD2 acted directly on the bone marrow to increase monocyte-macrophage progenitors. A transplantation assay further demonstrated that bone marrow from old mice facilitated hepatic collagen accumulation in young mice. Transient RvD2 treatment to mice transplanted with bone marrow from old mice prevented hepatic collagen accumulation. Together, this study demonstrates that RvD2-GPR18 signaling controls steatosis and fibrosis and provides a mechanistic-based therapy for promoting liver repair in aging.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Médula Ósea / Hígado Graso Límite: Aged / Animals / Humans / Middle aged Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Médula Ósea / Hígado Graso Límite: Aged / Animals / Humans / Middle aged Idioma: En Año: 2023 Tipo del documento: Article