Origin of interstitial fibroblasts in an accelerated model of angiotensin II-induced renal fibrosis

Jennifer L. Faulkner, Lisa M. Szcykalski, Fredyne Springer, Jeffrey L. Barnes

Resultado de la investigación: Articlerevisión exhaustiva

88 Citas (Scopus)

Resumen

To determine whether previous renal injury accelerates the progression, of glomeralosclerosis and interstitial fibrosis, we examined the effect of treating rats with angiotensin II after Habu venom injury. After initiating disease, we examined the origin of interstitial myofibroblasts by locating α-smooth muscle actin (α-SMA)-positive and Na+,K+-ATPase- positive cells relative to interstitial space, tubular epithelial cells, the tubular basement membrane (TBM), and vascular structures. Tubular epithelial-mesenchymal transition was also assessed by examining TBM integrity and by using Texas Red (TR)-dextran in intravital tracking experiments. The staining of α-SMA-positive myofibroblasts dramatically increased in peritubular interstitial spaces 48 hours after Habu venom plus angiotensin II, particularly in and around perivascalar and periglomerular regions, while tubular epithelial cells were α-SMA-negative. Na+,K +-ATPase-positive and TR-dextran-labeled cells were restricted to the tubular epithelium and excluded from the interstitium. By 7 and 14 days, expanded interstitial space contained only α-SMA-positive myofibroblasts without TR-dextran endocytic particles. Epithelium of atrophic tubules containing TR-dextran remained confined by surrounding interstitium and myofibroblasts. These studies indicate that early expansion of α-SMA-positive cells in the interstitium and loss of tubular area occur via encroachment of interstitial myofibroblasts from perivascular into atrophic tubular spaces rather than via epithelial-mesenchymal transition and migration of tubular cells through the TBM into the interstitium.

Idioma originalEnglish (US)
Páginas (desde-hasta)1193-1205
Número de páginas13
PublicaciónAmerican Journal of Pathology
Volumen167
N.º5
DOI
EstadoPublished - nov. 2005
Publicado de forma externa

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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