1.The Role of Mesothelial Cells in Liver Development, Injury, and Regeneration.
Gut and Liver 2016;10(2):166-176
Mesothelial cells (MCs) cover the surface of visceral organs and the parietal walls of cavities, and they synthesize lubricating fluids to create a slippery surface that facilitates movement between organs without friction. Recent studies have indicated that MCs play active roles in liver development, fibrosis, and regeneration. During liver development, the mesoderm produces MCs that form a single epithelial layer of the mesothelium. MCs exhibit an intermediate phenotype between epithelial cells and mesenchymal cells. Lineage tracing studies have indicated that during liver development, MCs act as mesenchymal progenitor cells that produce hepatic stellate cells, fibroblasts around blood vessels, and smooth muscle cells. Upon liver injury, MCs migrate inward from the liver surface and produce hepatic stellate cells or myofibroblast depending on the etiology, suggesting that MCs are the source of myofibroblasts in capsular fibrosis. Similar to the activation of hepatic stellate cells, transforming growth factor β induces the conversion of MCs into myofibroblasts. Further elucidation of the biological and molecular changes involved in MC activation and fibrogenesis will contribute to the development of novel approaches for the prevention and therapy of liver fibrosis.
Epithelial Cells/*physiology
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Epithelium/metabolism
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Hepatic Stellate Cells/*physiology
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Humans
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Liver/*cytology/injuries/*physiology
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Liver Cirrhosis/etiology/prevention & control
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Liver Regeneration/*physiology
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Mesenchymal Stromal Cells/physiology
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Myofibroblasts/physiology
2.Progress of autophagy in regulating liver homeostasis.
Hui HUANG ; Hongyan LI ; Wei ZOU
Chinese Journal of Biotechnology 2016;32(9):1185-1193
Liver is the largest human digestive gland and the most important metabolic organ. When autophagy was proposed during studying liver lysosomes in the 1960s, it was found that nutrient levels and hormones could influence autophagy activity. Recent studies show that autophagy is not only normal physiological processes, but also involved in the regulation of many pathological processes. This article summarizes the role of liver autophagy in the maintenance of homeostasis in the healthy liver, and provides new ideas for liver physiology and treating diseases associated with autophagy disorders.
Animals
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Autophagy
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Homeostasis
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Humans
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Liver
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physiology
3.Progress on relationship between exercise improving insulin resistance and AMP-activated protein kinase.
Acta Physiologica Sinica 2014;66(2):231-240
The AMP-activated protein kinase (AMPK) widely exists in skeletal muscle, liver, pancreas, adipose tissue and central nervous system. As a "cellular energy regulator", activation of AMPK can improve insulin resistance in various mechanisms. To overall understand the importance of AMPK in exercise, the article summarized the research progress on AMPK exercise activation in skeletal muscle, liver and adipose tissue as well as exercise improving cardiovascular insulin resistance by AMPK, and looked forward to the study future of AMPK exercise activation.
AMP-Activated Protein Kinases
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physiology
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Adipose Tissue
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physiology
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Exercise
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physiology
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Humans
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Insulin Resistance
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Liver
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physiology
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Muscle, Skeletal
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physiology
4.Research on liver regeneration driven by the amniotic membrane.
Jia XU ; Haitao ZHANG ; Ji LI ; Ning LI
Chinese Medical Journal 2014;127(7):1382-1384
Amnion
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metabolism
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physiology
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Female
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Hepatectomy
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Humans
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Liver Regeneration
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physiology
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Pregnancy
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Wound Healing
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physiology
6.Construction and experimental study on off-line hybrid bioartificial liver supporting system with human liver cell line.
Yi-Hui RONG ; Hong-Ling LIU ; Shao-Li YOU ; Wan-Shu LIU ; Yan HU ; Jun HOU ; Pan-Yong MAO ; Shao-Jie XIN
Chinese Journal of Experimental and Clinical Virology 2010;24(3):193-195
OBJECTIVETo construct an off-line hybrid bioartificial liver supporting system with human liver cell line, and study it's effect on the plasma from patients with liver failure.
METHODSWe established the bioreactor using Psu-2s (Fresenius) cultured with Hep G2 cell transfected with human augmenter of liver regeneration (hALR) gene, then constructed a hybrid bioartificial liver supporting system, at last using the bioartificial liver support system to purify the plasma treated 2 hours with serum bilirubin absorbent, separated from acute on chronic liver failure patients infected by hepatitis B virus.
RESULTSBioreactor was successful constructed. The cell viability in perigastrum of bioreactor is 85.2% and cell propagated rapidly. Before and after treating with bilirubin absorbent, serum total bilirubin was (176.19 +/- 54.14) micromol/L and (50.1 +/- 16.85) micromol/L respectively (P = 0.0002). While there were no significance difference in the level of albumin, urea and glucose. At the begin and end of treatment with bioartificial liver, serum total bilirubin was (50.10 +/- 16.85) micromol/L and (30.27 +/- 15.02) micromol/L respectively (P = 0.000), the urea and albumin increased, urea has significantly difference, but the change of albumin hasn't.
CONCLUSIONThe off-line hybrid bioartificial liver supporting system with human liver cell line were builded successfully and have synthesis and metabolism functions for acute on chronic liver failure patients.
Adult ; Artifacts ; Bilirubin ; metabolism ; Bioreactors ; standards ; Chimera ; End Stage Liver Disease ; physiopathology ; Hepatocytes ; metabolism ; physiology ; Humans ; Liver ; physiology ; Liver Failure ; Liver, Artificial ; utilization ; Male ; Middle Aged
7.A study on hepatic perfusion parameter calculation.
Fan PENG ; Bixian SHEN ; Zhenhua LIAO ; Weiqiang LIU
Journal of Biomedical Engineering 2013;30(6):1250-1253
Hepatic perfusion parameters play an important role in detecting and diagnosing diffusion diseases of liver. Based on a hemodynamic model. In this study, we described a fast and accurate method to calculate the perfusion parameters. First, we used a dual-input one-compartment kinetics model to illustrate the distribution of the contrast agent concentration among the body. Then, we used the Gaussian function to fit the scatter concentration data of portal vein and aorta, to obtain a liver agent concentration on function of time. Finally, we solved the model parameters by using Levenberg-Marquardt algorithm, and calculated the perfusion parameters. The results showed that the method proposed in this study could calculate the parameters precisely, and had a prosperous future application possibility.
Algorithms
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Contrast Media
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Hemodynamics
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Humans
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Liver
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physiology
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Models, Biological
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Perfusion
8.Prospect of bone morphogenetic protein 13 in liver diseases.
Yining LI ; Hong SHEN ; Frank J BURCZYNSKI ; Yuewen GONG
Journal of Central South University(Medical Sciences) 2012;37(1):1-5
Bone morphogenetic proteins (BMPs) belong to TGF-β superfamily and are a group of important cytokines involved in cell differentiation, proliferation and embryonic development. Multiple BMPs play important roles in several functions of vertebrates. Signaling pathway of BMPs is known to be mediated by Smad proteins, which include 8 members while Smad1, Smad5 and Smad8 are involved in BMPs signal transduction while Smad2 and Smad3 are mediated TGF-β signal transduction. Although several BMPs such as BMP4 and BMP9 have been documented in the liver, BMP13 has not been examined in the liver. BMP13 also known as growth differentiation factor (GDF)-6 or cartilage-derived morphogenetic protein (CDMP)-2 is one of the BMPs family members. Function of BMP13 has been investigated in bone and tendon repair. It can stimulate tendon-like cell proliferation. However, our recent findings revealed that there was expression of BMP13 in the liver and its expression was modulated during metabolic disorders. The current article is to understand biological function of BMP13 especially in the liver.
Bone Morphogenetic Proteins
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metabolism
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physiology
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Growth Differentiation Factor 6
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metabolism
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physiology
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Humans
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Liver
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metabolism
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Liver Diseases
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metabolism
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Smad Proteins
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metabolism
9.Exploration on central neurobiological mechanisms of Gan in taking charge of dispersion and regulating emotion.
Chinese Journal of Integrated Traditional and Western Medicine 2005;25(5):459-462
Methods and thoughts of the further research on central neurobiological mechanisms of Gan in taking charge of dispersion and regulating emotion are discussed. By applying the holistic approach and homeostasis theory, combined with modern psychological stress theory, the authors put forward their hypothesis of study. They offered that the TCM theory of "Gan takes charge of dispersion and could regulate emotion" is affirmatively to have certain mechanisms of central neurobiology. So, cut-in from the point of psychological stress reaction, adopting the research thoughts of "prescription-syndrome-therapeutic effectiveness--essence of Zang-Fu function", a model of chronic psychological stress reaction (CPSR) for imitating the process of comprehensive pathologic change due to Gan fails to take charge of dispersion and leads to emotional disorder was established. It is considered based on analysis of materials obtained from previous studies, that the central neurobiologic mechanism of so called dispersion, which Gan in charge of, is related to the regulation of hypothalamus-pitutary-adrenal gland axis. Concretely, the function of Gan in TCM may be, in the gross, related with the changes of multiple neurotransmitters and their synthetase produced in the process of CPSR (emotional disorder) regulation, such as neuropeptides, hormones, cyclic necleotide system and Fos protein expression, showing the characteristics of multiple links, multiple levels and multiple targets, with the effects involve several brain regions including various clusters of nuclei in hypothalamus, hippocampus and amygdala, etc.
Brain
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physiology
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Emotions
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Humans
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Liver
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physiology
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Medicine, Chinese Traditional
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Stress, Psychological