Your browser doesn't support javascript.
loading
Neutrophils Induce Astroglial Differentiation and Migration of Human Neural Stem Cells via C1q and C3a Synthesis.
Hooshmand, Mitra J; Nguyen, Hal X; Piltti, Katja M; Benavente, Francisca; Hong, Samuel; Flanagan, Lisa; Uchida, Nobuko; Cummings, Brian J; Anderson, Aileen J.
Afiliación
  • Hooshmand MJ; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA 92697; mitrah@uci.edu.
  • Nguyen HX; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, CA 92697.
  • Piltti KM; Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA 92697.
  • Benavente F; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA 92697.
  • Hong S; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, CA 92697.
  • Flanagan L; Department of Physical Medicine and Rehabilitation, University of California, Irvine, Irvine, CA 92697.
  • Uchida N; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA 92697.
  • Cummings BJ; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, CA 92697.
  • Anderson AJ; Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA 92697.
J Immunol ; 199(3): 1069-1085, 2017 08 01.
Article en En | MEDLINE | ID: mdl-28687659
Inflammatory processes play a key role in pathophysiology of many neurologic diseases/trauma, but the effect of immune cells and factors on neurotransplantation strategies remains unclear. We hypothesized that cellular and humoral components of innate immunity alter fate and migration of human neural stem cells (hNSC). In these experiments, conditioned media collected from polymorphonuclear leukocytes (PMN) selectively increased hNSC astrogliogenesis and promoted cell migration in vitro. PMN were shown to generate C1q and C3a; exposure of hNSC to PMN-synthesized concentrations of these complement proteins promoted astrogliogenesis and cell migration. Furthermore, in vitro, Abs directed against C1q and C3a reversed the fate and migration effects observed. In a proof-of-concept in vivo experiment, blockade of C1q and C3a transiently altered hNSC migration and reversed astroglial fate after spinal cord injury. Collectively, these data suggest that modulation of the innate/humoral inflammatory microenvironment may impact the potential of cell-based therapies for recovery and repair following CNS pathology.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complemento C1q / Complemento C3a / Diferenciación Celular / Astrocitos / Células-Madre Neurales / Neutrófilos Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complemento C1q / Complemento C3a / Diferenciación Celular / Astrocitos / Células-Madre Neurales / Neutrófilos Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2017 Tipo del documento: Article