DI-UMONS : Dépôt institutionnel de l’université de Mons

Recherche transversale
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2006-07-01 - Article/Dans un journal avec peer-review - Anglais - 12 page(s)

Declèves Anne-Emilie, Caron Nathalie, Nonclercq Denis , Legrand Alexandre , Toubeau Gérard, Kramp Ronald, Flamion Bruno, "Dynamics of hyaluronan, CD44 and inflammarory cells in the rat kidney after ischemia/reperfusion injury" in International Journal of Molecular Medicine, 18, 1, 83-94

  • Edition : Professor D A Spandidos, Athens (Greece)
  • Codes CREF : Histologie (DI3212), Médecine pathologie humaine (DI3300)
  • Unités de recherche UMONS : Physiologie et réadaptation respiratoire (M117), Histologie (M118)
  • Instituts UMONS : Institut des Sciences et Technologies de la Santé (Santé)
Texte intégral :

Abstract(s) :

(Anglais) Ischemia/reperfusion (I/R) injury in the kidney involves hemodynamic and cellular dysfunctions as well as leukocyte infiltration. Functional recovery occurs via cell proliferation and/or migration. To determine the roles of hyaluronan (HA) and its main receptor CD44 in renal postischemic processes, we compared their localization and expression with that of neutrophils, macrophages, and PCNA-positive (regenerative) cells as characterized by immunohistochemistry, up to 28 days after I/R in uninephrectomized rats. Observations covered all kidney zones, i.e. cortex (C), outer and inner stripes of outer medulla (OSOM, ISOM), and inner medulla (IM). In controls, HA was localized to the interstitium of IM and ISOM, and CD44 was mostly present on the basolateral membranes of collecting ducts in ISOM, the thin descending limb of Henle's loop and macula densa cells. After I/R, HA and CD44 staining appeared in C and OSOM at 12 h and persisted throughout the regenerative period, i.e. until day 7. Thereafter, they regressed but remained associated with remodeling areas. CD44 expression was found de novo on the apical pole of regenerating, not fully differentiated tubular cells and on some interstitial cells. It was prominent on all infiltrating neutrophils, as soon as 2 h post-I/R, and on 30% of the macrophages, including those in late HA-rich inflammatory granulomas. CD44 is probably involved in early leukocyte infiltration, in tubular regeneration, and in macrophage activity, while HA modifies the physico-chemical environment of interstitial and migrating cells. Based on its presence in remodeling areas, the HA-CD44 pair may be implicated in persistent postichemic inflammation as observed in chronic allograft nephropathy.

Identifiants :
  • ISSN : 1107-3756
  • PMID : 16786159