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  4. Potential of bioengineering processes for therapeutic repopulation of the liver with cells
 
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Potential of bioengineering processes for therapeutic repopulation of the liver with cells

Journal
Biotechnology and Bioprocess Engineering
Journal Volume
12
Journal Issue
1
Pages
1-8
Date Issued
2007
Author(s)
YAO-MING WU  
Kumaran V.
Benten D.
Gupta S.
DOI
10.1007/BF02931796
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-33847794434&doi=10.1007%2fBF02931796&partnerID=40&md5=c82ed6a92b1a4811a10a0b91e4ebbfe1
https://scholars.lib.ntu.edu.tw/handle/123456789/457913
Abstract
Multiple unique aspects of liver biology make this organ an excellent paradigm for novel cell and gene therapy applications. In recent years, insights were obtained into how transplanted cells engraft and proliferate in the liver, including in the context of pre-existing disease. Also, a variety of animal models were studied to establish the basis of cell and gene therapy applications in specific disorders. Through ongoing research activity, additional mechanisms in liver repopulation have been uncovered, where manipulation of specific cell compartments and cellular processes, e.g., those aimed at extracellular matrix component receptors or soluble signals in transplanted and native cells can be exploited for enhancing cell engraftment and proliferation. Such studies demonstrate the possibility of applying biotechnology and/ or bioengineering principles to organ replacement aimed at cell and gene therapy. Joining of these disciplines with research in stem cell biology, particularly in efforts concerning targeting of transplanted stem cells to given organs with achievement of lineage-specific cell differentiation and function, will be particularly important for future cell and gene therapy applications. This review offers an overview of relevant mechanisms in liver repopulation. ? KSBB.
SDGs

[SDGs]SDG3

Other Subjects
biomaterial; cyclophosphamide; cyclosporin; doxorubicin; fibroblast growth factor; glyceryl trinitrate; matrix metalloproteinase; mycophenolic acid 2 morpholinoethyl ester; phentolamine; polymer; rapamycin; scatter factor; tacrolimus; tissue inhibitor of metalloproteinase; bioengineering; biotechnology; cell activation; cell differentiation; cell function; cell interaction; cell population; cell proliferation; cell survival; drug delivery system; embryonic stem cell; extracellular matrix; hepatocyte transplantation; human; Kupffer cell; liver blood flow; liver disease; liver graft rejection; liver ischemia; liver regeneration; nonhuman; nonviral gene therapy; review; stem cell transplantation; survival time; Animalia
Type
review

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