Adult reserve stem cells and their potential for tissue engineering

被引:0
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作者
Henry E. Young
Cecile Duplaa
Marina Romero-Ramos
Marie-Francoise Chesselet
Patrick Vourc'h
Michael J. Yost
Kurt Ericson
Louis Terracio
Takayuki Asahara
Haruchika Masuda
Sayaka Tamura-Ninomiya
Kristina Detmer
Robert A. Bray
Timothy A. Steele
Douglas Hixson
Mohammad el-Kalay
Brain W. Tobin
Roy D. Russ
Michael N. Horst
Julie A. Floyd
Nicholas L. Henson
Kristina C. Hawkins
Jaime Groom
Amar Parikh
Lisa Blake
Laura J. Bland
Angela J. Thompson
Amy Kirincich
Catherine Moreau
John Hudson
Frank P. Bowyer
T. J. Lin
Asa C. Black
机构
[1] Mercer University School of Medicine,Division of Basic Medical Sciences
[2] Mercer University School of Medicine,Department of Pediatrics
[3] Mercer University School of Medicine,Department of Obstetrics and Gynecology
[4] Mercer University School of Medicine,Department of Internal Medicine
[5] INSERM U441,Department of Neurology, UCLA School of Medicine
[6] Reed Neurological Research Center,Department of Surgery
[7] University of South Carolina School of Medicine,Cardiovascular Research and Medicine, Tufts University School of Medicine
[8] New York University College of Dentistry,Department of Pathology and Laboratory Medicine
[9] Elizabeth's Medical Center,Department of Medicine
[10] Kobe Institute of Biomedical Research and Innovation/RIKEN Center of Developmental Biology,undefined
[11] Chuo,undefined
[12] Emory University Hospital,undefined
[13] Des Moines University-Osteopathic Medical Center,undefined
[14] Brown University,undefined
[15] MorphoGen Pharmaceuticals,undefined
[16] Inc.,undefined
来源
关键词
Adult; pluripotent; stem cells; mammals; humans; embyonic; mesenchymal; neurodegenerative; diabetes; infarction;
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摘要
Tissue restoration is the process whereby multiple damaged cell types are replaced to restore the histoarchitecture and function to the tissue. Several theories, have been proposed to explain the phenomenon of tissue restoration in amphibians and in animals belonging to higher order. These theories include dedifferentiation of damaged tissues, transdifferentiation of lineage-committed progenitor cells, and activation of reserve, precursor cells. Studies by Young et al. and others demonstrated that connective tissue compartments throughout postnatal individuals contain reserve precursor cells. Subsequent repetitive single cell-cloning and cell-sorting studies revealed that these reserve precursor cells consisted of multiple populations of cells, including, tissue-specific progenitor cells, germ-layer lineage stem cells, and pluripotent stem cells. Tissue-specific progenitor cells display various capacities for differentiation, ranging from unipotency (forming a single cell type) to multipotency (forming multiple cell types). However, all progenitor cells demonstrate a finite life span of 50 to 70 population doublings before programmed cell senescence and cell death occurs. Germ-layer lineage stem cells can form a wider range of cell types than a progenitor cell. An individual germ-layer lineage stem cell can form all cells types within its respective germ-layer lineage (i.e., ectoderm, mesoderm, or endoderm). Pluripotent stem cells can form a wider range of cell types than a single germ-layer lineage stem cell. A single pluripotent stem cell can form cells belonging to all three germ layer lineages. Both germ-layer lineage stem cells and pluripotent stem cells exhibit extended capabilities for self-renewal, far surpassing the limited life span of progenitor cells (50–70 population doublings). The authors propose that the activation of quiescent tissue-specific progenitor cells, germ-layer lineage stem cells, and/or pluripotent stem cells may be a potential explanation, along with dedifferentiation and transdifferentiation, for the process of tissue restoration. Several model systems are currently being investigated to determine the possibilities of using these adult quiescent reserve precursor cells for tissue engineering.
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页码:1 / 80
页数:79
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