Modulation of hepatic stellate cells and reversibility of hepatic fibrosis
Creators
- 1. Faculty of Graduate Studies of Guangxi University of Chinese Medicine, Nanning 530001, Guangxi Zhuang Autonomous Region (China)
- 2. Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, 10 East China Road, Nanning 530011, Guangxi Zhuang Autonomous Region (China)
- 3. Guangxi University of Chinese Medicine, Nanning 530001, Guangxi Zhuang Autonomous Region (China)
Description
Hepatic fibrosis (HF) is the pathological component of a variety of chronic liver diseases. Hepatic stellate cells (HSC) are the main collagen-producing cells in the liver and their activation promotes HF. If HSC activation and proliferation can be inhibited, HF occurrence and development can theoretically be reduced and even reversed. Over the past ten years, a number of studies have addressed this process, and here we present a review of HSC modulation and HF reversal. - Highlights: • We present a review of the modulation of hepatic stellate cells (HSC) and reversibility of hepatic fibrosis (HF). • HSC are the foci of HF occurrence and development, HF could be prevented and treated by modulating HSC. • If HSC activation and proliferation can be inhibited, HF could theoretically be inhibited and even reversed. • Prevention or reversal of HSC activation, or promotion of HSC apoptosis, immune elimination, and senescence may prevent, inhibit or reverse HF.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.yexcr.2017.02.038Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2017.02.038;
- PII
- S0014-4827(17)30092-7;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 352
- Journal Issue
- 2
- Journal Page Range
- p. 420-426
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48098505
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL TISSUES; APOPTOSIS; COLLAGEN; FIBROSIS; HYDROFLUORIC ACID; INTERFERON; LIGANDS; LIVER; MEDICINE; MODULATION; NECROSIS; NEOPLASMS; PLANT GROWTH; RADIOPROTECTIVE SUBSTANCES; RECEPTORS; RETINOIC ACID; REVIEWS
- Descriptors DEC
- BODY; CARBOXYLIC ACID ESTERS; DIGESTIVE SYSTEM; DISEASES; DOCUMENT TYPES; DRUGS; ESTERS; FLUORINE COMPOUNDS; GLANDS; GROWTH; GROWTH FACTORS; HALOGEN COMPOUNDS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; LYMPHOKINES; MEMBRANE PROTEINS; MITOGENS; ORGANIC COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; PROTEINS; RESPONSE MODIFYING FACTORS; SCLEROPROTEINS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.