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...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
F1000 Research Ltd
2016-07-01
|
Series: | F1000Research |
Subjects: | |
Online Access: | http://f1000research.com/articles/5-1749/v1 |
id |
doaj-83f0089a32924d4b919f48992fe5768c |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT rossdobie hominginonthehepaticscarrecentadvancesincellspecifictargetingofliverfibrosisversion1referees3approved AT neilchenderson hominginonthehepaticscarrecentadvancesincellspecifictargetingofliverfibrosisversion1referees3approved |
_version_ |
1724612012770590720 |