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Interstitial expression of heat‐shock protein 47 correlates with capillary deposition of complement split product C4d in chronic allograft nephropathy
Author(s) -
Ohba Kojiro,
Miyata Yasuyoshi,
Koga Shigehiko,
Nishikido Masaharu,
Kanetake Hiroshi,
Nazneen Arifa,
Razzaque Mohammed S,
Taguchi Takashi
Publication year - 2005
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/j.1399-0012.2005.00426.x
Subject(s) - medicine , pathology , myofibroblast , immunohistochemistry , peritubular capillaries , cd68 , fibrosis , chronic allograft nephropathy , kidney , nephropathy , biopsy , kidney transplantation , diabetes mellitus , endocrinology
Background: Chronic allograft nephropathy (CAN), associated with late‐allograft dysfunction is caused by alloantigen‐dependent and ‐independent mechanisms, and eventually leads to interstitial fibrosis (ci). Activation of complement cascade is considered to be a poor prognostic marker of graft survival. This study was designed to examine the relationship between the expression of C4d and heat‐shock protein 47 (HSP47, a collagen‐specific chaperone) in the development of interstitial fibroproliferative lesions in CAN. Methods: Sixty‐three renal allograft biopsy specimens, obtained from 48 patients, were examined for the expression of C4d, HSP47, CD68 and α ‐smooth muscle actin ( α ‐SMA) by immunohistochemistry. Double‐staining was performed to determine the colocalization of C4d and HSP47. The relationship of between the expression of C4d, HSP47, CD68 and α ‐SMA and the clinical and histopathological parameters were statistically analysed. Results: No expression of C4d was noted in the tubulointerstitium including peritubular capillary (PTC) of the control kidney. C4d was expressed in PTC in one‐third of allograft renal tissues with morphological evidences of CAN. The interstitial cells around the fibrotic areas of the PTC of CAN were positive for the expression of HSP47. The deposition of C4d in PTC correlated with interstitial expression of HSP47 around the PTC. Most HSP47 expressing cells were phenotypically altered myofibroblasts, as determined by the dual staining of α ‐SMA. Conclusions: The increased expression of HSP47 positively correlated with the expression of C4d in PTC, and might contribute to the progression of interstitial ci in CAN.