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Hepatic Regeneration in Cirrhosis
Ankur Jindal1, Rakesh K Jagdish2, Anupam Kumar3
1Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi 110070, India.
Journal of Clinical and Experimental Hepatology
|May 10, 2022
Summary
Harnessing liver regeneration through stem cell therapy offers a promising alternative to liver transplantation for end-stage liver disease. Research focuses on hepatic progenitor and bone marrow stem cells to restore liver function.
Area of Science:
- Hepatology and Regenerative Medicine
- Stem Cell Biology and Therapeutics
Background:
- End-stage liver disease involves significant hepatocyte death, leading to decompensation and organ failure.
- Cirrhosis results from functional hepatocyte loss and excessive scarring, with limited self-renewal capacity.
- Orthotropic liver transplantation is curative but limited by donor organ availability and lifelong immunosuppression risks.
Purpose of the Study:
- To investigate the therapeutic potential of hepatic progenitor cells and bone marrow-derived stem cells in liver regeneration.
- To explore cell-based therapies as an alternative to liver transplantation for advanced cirrhosis.
Main Methods:
- Characterizing the role of hepatic progenitor cells and bone marrow-derived stem cells in liver regeneration.
- Developing techniques for cell proliferation, differentiation, and storage for therapeutic applications.
- Evaluating the functionality of transplanted cells for clinical use.
Main Results:
- Significant research advancements over two decades have refined cell-based therapy techniques.
- Understanding of cell functionality for clinical applications has been improved.
- Cell-based therapies are still in experimental stages, requiring further clinical trials.
Conclusions:
- Cell-based therapies hold promise for treating end-stage liver disease by aiding liver regeneration.
- Further research and clinical trials are essential to establish the efficacy and safety of these experimental treatments.
- The focus is on differentiating various cell sources into functional liver cells or using growth factors for ex-vivo expansion.
Keywords:
Ang2, angiopoietin 2BM, Bone marrowBM-MNCs, bone marrow mononuclear cellsBMSC, bone marrow stem cellsDAMPs, Damage associated molecular patternsEPCs, endothelial progenitor cellsESRP2, epithelial splicing regulatory protein 2GCSFHGF, hepatocyte growth factorHPC, Hepatocyte progenitor cellsHSCs, hematopoietic stem cellsHh, HedgehogHybHP, hybrid periportal hepatocytesMMP, matrix metalloproteaseMSCs, mesenchymal stromal cellsOLT, Orthotropic liver transplantationPAMPs, Pathogen associated molecular patternsSAH, severe alcoholic hepatitisSDF1, stromal-derived factor 1TNFSF12, tumor necrosis factor ligand superfamily member 12Terthigh, high Telomerase reverse transcriptase[Hnf4a], Hepatocyte Nuclear Factor 4 Alpha[Mfsd2a], Major Facilitator Superfamily Domain containing 2Aacute liver failurechronic liver diseaseshepatocyte transplantliver regenerationRelated Concept Videos
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