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Neutrophil and monocyte kinetics play critical roles in mouse peritoneal adhesion formation.
Tsai, Jonathan M; Shoham, Maia; Fernhoff, Nathaniel B; George, Benson M; Marjon, Kristopher D; McCracken, Melissa N; Kao, Kevin S; Sinha, Rahul; Volkmer, Anne Kathrin; Miyanishi, Masanori; Seita, Jun; Rinkevich, Yuval; Weissman, Irving L.
Afiliación
  • Tsai JM; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Shoham M; Department of Developmental Biology, School of Medicine, Stanford University, Stanford, CA.
  • Fernhoff NB; Department of Pathology, Brigham and Women's Hospital, Boston, MA.
  • George BM; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Marjon KD; Institute for Stem Cell Biology and Regenerative Medicine and.
  • McCracken MN; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Kao KS; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Sinha R; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Volkmer AK; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Miyanishi M; Institute for Stem Cell Biology and Regenerative Medicine and.
  • Seita J; Department of Gynecology and Obstetrics, University Hospital Düsseldorf, Düsseldorf, Germany.
  • Rinkevich Y; Center for Developmental Biology, RIKEN, Kobe, Japan.
  • Weissman IL; AI based Healthcare and Medical Data Analysis Standardization Unit, Medical Sciences Innovation Hub Program, RIKEN, Tokyo, Japan; and.
Blood Adv ; 3(18): 2713-2721, 2019 09 24.
Article en En | MEDLINE | ID: mdl-31519647
Peritoneal adhesions are pathological fibroses that ensnare organs after abdominal surgery. This dense connective tissue can cause small bowel obstruction, female infertility, and chronic abdominal pain. The pathogenesis of adhesions is a fibrotic response to tissue damage coordinated between mesothelial cells, fibroblasts, and immune cells. We have previously demonstrated that peritoneal adhesions are a consequence of mechanical injury to the mesothelial layer sustained during surgery. Neutrophils are among the first leukocytes involved in the early response to tissue damage. Here, we show that when subjected to mechanical stress, activated mesothelial cells directly recruit neutrophils and monocytes through upregulation of chemokines such as CXCL1 and monocyte chemoattractant protein 1 (MCP-1). We find that neutrophils within the adhesion sites undergo cell death and form neutrophil extracellular traps (NETosis) that contribute to pathogenesis. Conversely, tissue-resident macrophages were profoundly depleted throughout the disease time course. We show that this is distinct from traditional inflammatory kinetics such as after sham surgery or chemically induced peritonitis, and suggest that adhesions result from a primary difference in inflammatory kinetics. We find that transient depletion of circulating neutrophils significantly decreases adhesion burden, and further recruitment of monocytes with thioglycolate or MCP-1 also improves outcomes. Our findings suggest that the combination of neutrophil depletion and monocyte recruitment is sufficient to prevent adhesion formation, thus providing insight for potential clinical interventions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monocitos / Adherencias Tisulares / Neutrófilos Límite: Animals / Female / Humans Idioma: En Revista: Blood Adv Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monocitos / Adherencias Tisulares / Neutrófilos Límite: Animals / Female / Humans Idioma: En Revista: Blood Adv Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos