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Inhibition of Soluble Stem Cell Factor Promotes Intestinal Mucosal Repair.
Garcia-Hernandez, Vicky; Raya-Sandino, Arturo; Azcutia, Veronica; Miranda, Jael; Kelm, Matthias; Flemming, Sven; Birkl, Dorothee; Quiros, Miguel; Brazil, Jennifer C; Parkos, Charles A; Nusrat, Asma.
Afiliação
  • Garcia-Hernandez V; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Raya-Sandino A; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Azcutia V; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Miranda J; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Kelm M; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Flemming S; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Birkl D; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Quiros M; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Brazil JC; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Parkos CA; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Nusrat A; Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
Inflamm Bowel Dis ; 29(7): 1133-1144, 2023 07 05.
Article em En | MEDLINE | ID: mdl-36688460
ABSTRACT

BACKGROUND:

Incidences of inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, are escalating worldwide and can be considered a global public health problem. Given that the gold standard approach to IBD therapeutics focuses on reducing the severity of symptoms, there is an urgent unmet need to develop alternative therapies that halt not only inflammatory processes but also promote mucosal repair. Previous studies have identified increased stem cell factor (SCF) expression in inflamed intestinal mucosal tissues. However, the role that SCF plays in mediating intestinal inflammation and repair has not been explored.

METHODS:

Changes in the expression of SCF were evaluated in the colonic tissue of healthy mice and during dextran sodium sulfate (DSS)-induced colitis. Furthermore, mucosal wound healing and colitis severity were analyzed in mice subjected to either mechanical biopsy or DSS treatment, respectively, following intestinal epithelial cell-specific deletion of SCF or anti-SCF antibody administration.

RESULTS:

We report robust expression of SCF by intestinal epithelial cells during intestinal homeostasis with a switch to immune cell-produced SCF during colitis. Data from mice with intestinal epithelial cell-specific deletion of SCF highlight the importance of immune cell-produced SCF in driving the pathogenesis of colitis. Importantly, antibody-mediated neutralization of total SCF or the specific SCF248 isoform decreased immune cell infiltration and enhanced mucosal wound repair following biopsy-induced colonic injury or DSS-induced colitis.

CONCLUSIONS:

These data demonstrate that SCF functions as a pro-inflammatory mediator in mucosal tissues and that specific neutralization of SCF248 could be a viable therapeutic option to reduce intestinal inflammation and promote mucosal wound repair in individuals with IBD.
Our investigation demonstrates that blocking cleavable SCF248 isoform by administration of specific stem cell factor antibodies enhances healing of the intestinal mucosa and restores critical barrier function, suggesting an alternative therapeutic option to treat individuals with active IBD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Colite Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Colite Idioma: En Ano de publicação: 2023 Tipo de documento: Article