Your browser doesn't support javascript.
loading
The immune-stimulating peptide WKYMVm has therapeutic effects against ulcerative colitis
Experimental & Molecular Medicine ; : e40-2013.
Artículo en Inglés | WPRIM | ID: wpr-71809
ABSTRACT
In this study, we examined the therapeutic effects of an immune-stimulating peptide, WKYMVm, in ulcerative colitis. The administration of WKYMVm to dextran sodium sulfate (DSS)-treated mice reversed decreases in body weight, bleeding score and stool score in addition to reversing DSS-induced mucosa destruction and shortened colon. The WKYMVm-induced therapeutic effect against ulcerative colitis was strongly inhibited by a formyl peptide receptor (FPR) 2 antagonist, WRWWWW, indicating the crucial role of FPR2 in this effect. Mechanistically, WKYMVm effectively decreases intestinal permeability by stimulating colon epithelial cell proliferation. WKYMVm also strongly decreases interleukin-23 and transforming growth factor-beta production in the colon of DSS-treated mice. We suggest that the potent immune-modulating peptide WKYMVm and its receptor FPR2 may be useful in the development of efficient therapeutic agents against chronic intestinal inflammatory diseases.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Oligopéptidos / Permeabilidad / Colitis Ulcerosa / Adyuvantes Inmunológicos / Factor de Crecimiento Transformador beta / Colon / Células CACO-2 / Receptores de Formil Péptido / Proliferación Celular / Interleucina-23 Límite: Animales / Humanos Idioma: Inglés Revista: Experimental & Molecular Medicine Año: 2013 Tipo del documento: Artículo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Oligopéptidos / Permeabilidad / Colitis Ulcerosa / Adyuvantes Inmunológicos / Factor de Crecimiento Transformador beta / Colon / Células CACO-2 / Receptores de Formil Péptido / Proliferación Celular / Interleucina-23 Límite: Animales / Humanos Idioma: Inglés Revista: Experimental & Molecular Medicine Año: 2013 Tipo del documento: Artículo