| Autor: |
Lavaud, Stéphanie, Poirier, Bruno, Mandet, Chantal, Bélair, Marie-France, Irinopoulou, Théano, Heudes, Didier, Bazin, Raymond, Bariéty, Jean, Myara, Isaac, Chevalier, Jacques |
| Zdroj: |
American Journal of Physiology - Renal Physiology; April 2001, Vol. 280 Issue: 4 pF683-F694, 12p |
| Abstrakt: |
We examined the role of inflammation in the development of renal interstitial fibrosis in Zucker obese rats, which rapidly present kidney lesions in the absence of hypertension and hyperglycemia. Type I and III collagens were quantified using a polarized light and computer-assisted image analyzer. The expression of mRNA encoding matrix components, adhesion molecules, chemokines, and growth factors was followed by RT-PCR. The presence of synthesized proteins as well as lymphocytes and macrophages was determined by immunohistochemistry. Interstitial fibrosis developed in two phases. The first phase occurred as early as 3 mo and resulted from a neosynthesis of type III collagen and fibronectin and a reduction of extracellular matrix catabolism, in parallel with an overexpression of transforming growth factor-β1and in the absence of any lymphocyte or macrophage infiltration. After 6 mo, interstitial fibrosis worsened with a large accumulation of type I collagen, concomitantly with a large macrophage infiltration. Thus inflammation cannot explain the onset of interstitial fibrosis that developed in young, insulinoresistant, normoglycemic, obese Zucker rats but aggravated this process afterward. |
| Databáze: |
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