Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Banco de datos
Tipo del documento
Publication year range
1.
J Immunol ; 180(8): 5707-19, 2008 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-18390756

RESUMEN

Macrophages derived from human blood monocytes perform many tasks related to tissue injury and repair. The main effect of macrophages on the extracellular matrix is considered to be destructive in nature, because macrophages secrete metalloproteinases and ingest foreign material as part of the remodeling process that occurs in wound healing and other pathological conditions. However, macrophages also contribute to the extracellular matrix and hence to tissue stabilization both indirectly, by inducing other cells to proliferate and to release matrix components, and directly, by secreting components of the extracellular matrix such as fibronectin and type VIII collagen, as we have recently shown. We now report that monocytes and macrophages express virtually all known collagen and collagen-related mRNAs. Furthermore, macrophages secrete type VI collagen protein abundantly, depending upon their mode of activation, stage of differentiation, and cell density. The primary function of type VI collagen secreted by macrophages appears to be modulation of cell-cell and cell-matrix interactions. We suggest that the production of type VI collagen is a marker for a nondestructive, matrix-conserving macrophage phenotype that could profoundly influence physiological and pathophysiological conditions in vivo.


Asunto(s)
Colágeno Tipo VI/biosíntesis , Colágeno/biosíntesis , Proteínas de la Matriz Extracelular/metabolismo , Macrófagos/metabolismo , Monocitos/metabolismo , Secuencia de Aminoácidos , Línea Celular , Células Cultivadas , Colágeno/sangre , Colágeno/genética , Colágeno Tipo VI/sangre , Colágeno Tipo VI/genética , Fibroblastos/metabolismo , Humanos , Macrófagos/ultraestructura , Microscopía Electrónica de Rastreo , Datos de Secuencia Molecular , Miocitos del Músculo Liso/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Receptores de Superficie Celular/metabolismo
SELECCIÓN DE REFERENCIAS
Detalles de la búsqueda