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Insulin-Like Growth Factor I (IGF-I) Expressed from an AAV1 Vector Leads to a Complete Reversion of Liver Cirrhosis in Rats
by
Quiroga, Jorge
, Fortes, Puri
, Enguita, Mónica
, Prieto, Jesús
, Sobrevals, Luciano
in
Actin
/ Adeno-associated virus
/ Animal tissues
/ Biology and Life Sciences
/ Cancer therapies
/ Carbon tetrachloride
/ Cirrhosis
/ Collagen
/ Connective tissue growth factor
/ Connective tissues
/ Expression vectors
/ Fibrosis
/ Gene expression
/ Gene therapy
/ Hepatitis
/ Hepatocyte growth factor
/ Hepatocytes
/ Hepatology
/ Homeostasis
/ Inflammation
/ Insulin
/ Insulin-like growth factor I
/ Insulin-like growth factors
/ Liver
/ Liver cancer
/ Liver cirrhosis
/ Medical research
/ Medicine and Health Sciences
/ Molecular chains
/ Muscles
/ Rats
/ Research and Analysis Methods
/ Retroviridae
/ Reversion
/ Rodents
/ Smooth muscle
/ Stellate cells
/ Therapeutic applications
/ Transforming growth factor-b
/ Transplants & implants
/ Tumor necrosis factor-α
/ Vascular endothelial growth factor
/ Viruses
2016
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Insulin-Like Growth Factor I (IGF-I) Expressed from an AAV1 Vector Leads to a Complete Reversion of Liver Cirrhosis in Rats
by
Quiroga, Jorge
, Fortes, Puri
, Enguita, Mónica
, Prieto, Jesús
, Sobrevals, Luciano
in
Actin
/ Adeno-associated virus
/ Animal tissues
/ Biology and Life Sciences
/ Cancer therapies
/ Carbon tetrachloride
/ Cirrhosis
/ Collagen
/ Connective tissue growth factor
/ Connective tissues
/ Expression vectors
/ Fibrosis
/ Gene expression
/ Gene therapy
/ Hepatitis
/ Hepatocyte growth factor
/ Hepatocytes
/ Hepatology
/ Homeostasis
/ Inflammation
/ Insulin
/ Insulin-like growth factor I
/ Insulin-like growth factors
/ Liver
/ Liver cancer
/ Liver cirrhosis
/ Medical research
/ Medicine and Health Sciences
/ Molecular chains
/ Muscles
/ Rats
/ Research and Analysis Methods
/ Retroviridae
/ Reversion
/ Rodents
/ Smooth muscle
/ Stellate cells
/ Therapeutic applications
/ Transforming growth factor-b
/ Transplants & implants
/ Tumor necrosis factor-α
/ Vascular endothelial growth factor
/ Viruses
2016
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Insulin-Like Growth Factor I (IGF-I) Expressed from an AAV1 Vector Leads to a Complete Reversion of Liver Cirrhosis in Rats
by
Quiroga, Jorge
, Fortes, Puri
, Enguita, Mónica
, Prieto, Jesús
, Sobrevals, Luciano
in
Actin
/ Adeno-associated virus
/ Animal tissues
/ Biology and Life Sciences
/ Cancer therapies
/ Carbon tetrachloride
/ Cirrhosis
/ Collagen
/ Connective tissue growth factor
/ Connective tissues
/ Expression vectors
/ Fibrosis
/ Gene expression
/ Gene therapy
/ Hepatitis
/ Hepatocyte growth factor
/ Hepatocytes
/ Hepatology
/ Homeostasis
/ Inflammation
/ Insulin
/ Insulin-like growth factor I
/ Insulin-like growth factors
/ Liver
/ Liver cancer
/ Liver cirrhosis
/ Medical research
/ Medicine and Health Sciences
/ Molecular chains
/ Muscles
/ Rats
/ Research and Analysis Methods
/ Retroviridae
/ Reversion
/ Rodents
/ Smooth muscle
/ Stellate cells
/ Therapeutic applications
/ Transforming growth factor-b
/ Transplants & implants
/ Tumor necrosis factor-α
/ Vascular endothelial growth factor
/ Viruses
2016
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Insulin-Like Growth Factor I (IGF-I) Expressed from an AAV1 Vector Leads to a Complete Reversion of Liver Cirrhosis in Rats
Journal Article
Insulin-Like Growth Factor I (IGF-I) Expressed from an AAV1 Vector Leads to a Complete Reversion of Liver Cirrhosis in Rats
2016
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Overview
IGF-I modulates liver tissue homeostasis. It is produced by hepatocytes and signals within the liver through IGF-I receptor expressed on hepatic stellate cells (HSCs). Liver cirrhosis is characterized by marked IGF-I deficiency. Here we compared the effect of two different gene therapy vectors encoding IGF-I as a potential treatment for cirrhotic patients. Rats with carbon tetrachloride-induced liver cirrhosis were treated with controls or with adeno-associated virus 1 (AAV) or simian virus 40 (SV40) vectors expressing IGF-I (AAVIGF-I or SVIGF-I) and molecular and histological studies were performed at 4 days, 8 weeks and 16 weeks. Increased levels of IGF-I were observed in the liver as soon as 4 days after vector administration. Control cirrhotic rats showed increased hepatic expression of pro-inflammatory and pro-fibrogenic factors including transforming growth factor beta (TGFβ), tumor necrosis factor-alpha (TNFα), connective tissue growth factor (CTGF), and vascular endothelial growth factor (VEGF) together with upregulation of α-smooth muscle actin (αSMA), a marker of HSC activation. In IGF-I-treated rats the levels of all these molecules were similar to those of healthy controls by week 8 post-therapy. Of note, the decline of TGFβ, CTGF, VEGF and αSMA expression was more rapid in AAVIGF-I treated animals reaching statistical significance by day 4 post-therapy. IGF-I-treated rats showed similar improvement of liver function tests in parallel with upregulation of hepatocyte nuclear factor 4α (HNF4α), a factor that promotes hepatocellular differentiation. A significant decrease of liver fibrosis, accompanied by upregulation of the hepatoprotective and anti-fibrogenic hepatocyte growth factor (HGF), occurred in all IGF-I-treated rats but complete reversal of liver cirrhosis took place only in AAVIGF-I group. Therefore, AAVIGF-I reverts liver cirrhosis in rats, a capability which deserves clinical testing.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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