Abstract BACKGROUND/AIMS: In kidney transplants, the renin-angiotensin system (RAS) is involved in systemic and local changes that may induce fibrosis. Our aim was to use gene expression and immunohistochemical analysis to investigate the RAS and several factors involved in the fibrogenic cascade in allograft biopsies. METHODS: We considered 43 donor biopsies (T0), 18 biopsies obtained for diagnostic purposes (Td) and 24 protocol biopsies (Tp) taken 2 months after transplantation in patients with stable renal function. Morphometric alpha SMA and TGF beta 1 analysis, and Masson's Trichrome staining were performed. mRNA levels of angiotensinogen, renin, ACE, AT1-R, AT2-R, TGF beta 1, BMP-7, Coll III, fibronectin and alpha SMA were analyzed by real-time RT/PCR. MDRD a year after the transplant was also considered. RESULTS: Significantly higher levels of AT1-R and alpha SMA transcripts were found in Tp than in T0. Regression analysis showed significant TGF beta 1-independent positive correlations between RAS and matrix components in T0 and Tp, but more evident in Tp, where a positive correlation between TGF beta 1 and Masson's Trichrome stained areas was also seen. CONCLUSION: Our results suggest that RAS and TGF beta 1-related fibrogenic loops are activated as early as 2 months after kidney transplantation.

Early activation of fibrogenesis in transplanted kidneys: A study on serial renal biopsies / DEL PRETE, Dorella; Ceol, Monica; Anglani, Franca; Vianello, Daniela; Tiralongo, Emilia; Valente, Marialuisa; Graziotto, Romina; Bonfante, Luciana; Scaparrotta, Giuseppe; Furian, Lucrezia; Rigotti, Paolo; Gambaro, Giovanni; D'Angelo, Angela. - In: EXPERIMENTAL AND MOLECULAR PATHOLOGY. - ISSN 0014-4800. - 87:2(2009), pp. 141-145. [10.1016/j.yexmp.2009.07.004]

Early activation of fibrogenesis in transplanted kidneys: A study on serial renal biopsies

RIGOTTI, PAOLO;
2009-01-01

Abstract

Abstract BACKGROUND/AIMS: In kidney transplants, the renin-angiotensin system (RAS) is involved in systemic and local changes that may induce fibrosis. Our aim was to use gene expression and immunohistochemical analysis to investigate the RAS and several factors involved in the fibrogenic cascade in allograft biopsies. METHODS: We considered 43 donor biopsies (T0), 18 biopsies obtained for diagnostic purposes (Td) and 24 protocol biopsies (Tp) taken 2 months after transplantation in patients with stable renal function. Morphometric alpha SMA and TGF beta 1 analysis, and Masson's Trichrome staining were performed. mRNA levels of angiotensinogen, renin, ACE, AT1-R, AT2-R, TGF beta 1, BMP-7, Coll III, fibronectin and alpha SMA were analyzed by real-time RT/PCR. MDRD a year after the transplant was also considered. RESULTS: Significantly higher levels of AT1-R and alpha SMA transcripts were found in Tp than in T0. Regression analysis showed significant TGF beta 1-independent positive correlations between RAS and matrix components in T0 and Tp, but more evident in Tp, where a positive correlation between TGF beta 1 and Masson's Trichrome stained areas was also seen. CONCLUSION: Our results suggest that RAS and TGF beta 1-related fibrogenic loops are activated as early as 2 months after kidney transplantation.
2009
Fibrosis
Gene expression
Immunohistochemistry
RAS
Renal biopsies
TGFβ1
Transplant
Adult
Biopsy
Fibrosis
Gene Expression
Humans
Immunohistochemistry
Kidney
Kidney Transplantation
Middle Aged
RNA
Messenger
Renin-Angiotensin System
Reverse Transcriptase Polymerase Chain Reaction
Transforming Growth Factor beta1
Gene Expression Profiling
Clinical Biochemistry
Molecular Biology
2734
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/156976
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