Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]

Despite the high prevalence of liver disease globally, there are currently no approved anti-fibrotic therapies to treat patients with liver fibrosis. A major goal in anti-fibrotic therapy is the development of drug delivery systems that allow direct targeting of the major pro-scarring cell populatio...

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Main Authors: Ross Dobie, Neil C. Henderson
Format: Article
Language:English
Published: F1000 Research Ltd 2016-07-01
Series:F1000Research
Subjects:
Online Access:http://f1000research.com/articles/5-1749/v1
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spelling doaj-83f0089a32924d4b919f48992fe5768c2020-11-25T03:21:59ZengF1000 Research LtdF1000Research2046-14022016-07-01510.12688/f1000research.8822.19497Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]Ross Dobie0Neil C. Henderson1MRC Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UKMRC Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UKDespite the high prevalence of liver disease globally, there are currently no approved anti-fibrotic therapies to treat patients with liver fibrosis. A major goal in anti-fibrotic therapy is the development of drug delivery systems that allow direct targeting of the major pro-scarring cell populations within the liver (hepatic myofibroblasts) whilst not perturbing the homeostatic functions of other mesenchymal cell types present within both the liver and other organ systems. In this review we will outline some of the recent advances in our understanding of myofibroblast biology, discussing both the origin of myofibroblasts and possible myofibroblast fates during hepatic fibrosis progression and resolution. We will then discuss the various strategies currently being employed to increase the precision with which we deliver potential anti-fibrotic therapies to patients with liver fibrosis.http://f1000research.com/articles/5-1749/v1Gastrointestinal PharmacologyGastrointestinal PhysiologyLiver Biology & PathobiologyPharmacokinetics & Drug Delivery
collection DOAJ
language English
format Article
sources DOAJ
author Ross Dobie
Neil C. Henderson
spellingShingle Ross Dobie
Neil C. Henderson
Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
F1000Research
Gastrointestinal Pharmacology
Gastrointestinal Physiology
Liver Biology & Pathobiology
Pharmacokinetics & Drug Delivery
author_facet Ross Dobie
Neil C. Henderson
author_sort Ross Dobie
title Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
title_short Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
title_full Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
title_fullStr Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
title_full_unstemmed Homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
title_sort homing in on the hepatic scar: recent advances in cell-specific targeting of liver fibrosis [version 1; referees: 3 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2016-07-01
description Despite the high prevalence of liver disease globally, there are currently no approved anti-fibrotic therapies to treat patients with liver fibrosis. A major goal in anti-fibrotic therapy is the development of drug delivery systems that allow direct targeting of the major pro-scarring cell populations within the liver (hepatic myofibroblasts) whilst not perturbing the homeostatic functions of other mesenchymal cell types present within both the liver and other organ systems. In this review we will outline some of the recent advances in our understanding of myofibroblast biology, discussing both the origin of myofibroblasts and possible myofibroblast fates during hepatic fibrosis progression and resolution. We will then discuss the various strategies currently being employed to increase the precision with which we deliver potential anti-fibrotic therapies to patients with liver fibrosis.
topic Gastrointestinal Pharmacology
Gastrointestinal Physiology
Liver Biology & Pathobiology
Pharmacokinetics & Drug Delivery
url http://f1000research.com/articles/5-1749/v1
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