Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004:280:71-109.
doi: 10.1007/978-3-642-18846-6_2.

Existence of reserve quiescent stem cells in adults, from amphibians to humans

Affiliations
Review

Existence of reserve quiescent stem cells in adults, from amphibians to humans

H E Young. Curr Top Microbiol Immunol. 2004.

Abstract

Several theories have been proposed to explain the phenomenon of tissue restoration in amphibians and higher order animals. These theories include dedifferentiation of damaged tissues, transdifferentiation of lineage-committed stem cells, and activation of quiescent stem cells. Young and colleagues demonstrated that connective tissues throughout the body contain multiple populations of quiescent lineage-committed progenitor stem cells and lineage-uncommitted pluripotent stem cells. Subsequent cloning and cell sorting studies identified quiescent lineage-uncommitted pluripotent mesenchymal stem cells, capable of forming any mesodermal cell type, and pluripotent epiblastic-like stem cells, capable of forming any somatic cell type. Based on their studies, they propose at least 11 categories of quiescent reserve stem cells resident within postnatal animals, including humans. These categories are pluripotent epiblastic-like stem cells, pluripotent ectodermal stem cells, pluripotent epidermal stem cells, pluripotent neuronal stem cells, pluripotent neural crest stem cells, pluripotent mesenchymal (mesodermal) stem cells, pluripotent endodermal stem cells, multipotent progenitor stem cells, tripotent progenitor stem cells, bipotent progenitor stem cells, and unipotent progenitor stem cells. Thus, activation of quiescent reserve stem cells, i.e., lineage-committed progenitor stem cells and lineage-uncommitted pluripotent stem cells, resident within the connective tissues could provide for the continual maintenance and repair of the postnatal organism after birth.

PubMed Disclaimer

Similar articles

  • Adult reserve stem cells and their potential for tissue engineering.
    Young HE, Duplaa C, Romero-Ramos M, Chesselet MF, Vourc'h P, Yost MJ, Ericson K, Terracio L, Asahara T, Masuda H, Tamura-Ninomiya S, Detmer K, Bray RA, Steele TA, Hixson D, el-Kalay M, Tobin BW, Russ RD, Horst MN, Floyd JA, Henson NL, Hawkins KC, Groom J, Parikh A, Blake L, Bland LJ, Thompson AJ, Kirincich A, Moreau C, Hudson J, Bowyer FP 3rd, Lin TJ, Black AC Jr. Young HE, et al. Cell Biochem Biophys. 2004;40(1):1-80. doi: 10.1385/CBB:40:1:1. Cell Biochem Biophys. 2004. PMID: 14983110 Review.
  • Adult stem cells.
    Young HE, Black AC Jr. Young HE, et al. Anat Rec A Discov Mol Cell Evol Biol. 2004 Jan;276(1):75-102. doi: 10.1002/ar.a.10134. Anat Rec A Discov Mol Cell Evol Biol. 2004. PMID: 14699636 Review.
  • Clonogenic analysis reveals reserve stem cells in postnatal mammals. II. Pluripotent epiblastic-like stem cells.
    Young HE, Duplaa C, Yost MJ, Henson NL, Floyd JA, Detmer K, Thompson AJ, Powell SW, Gamblin TC, Kizziah K, Holland BJ, Boev A, Van De Water JM, Godbee DC, Jackson S, Rimando M, Edwards CR, Wu E, Cawley C, Edwards PD, Macgregor A, Bozof R, Thompson TM, Petro GJ Jr, Shelton HM, McCampbell BL, Mills JC, Flynt FL, Steele TA, Kearney M, Kirincich-Greathead A, Hardy W, Young PR, Amin AV, Williams RS, Horton MM, McGuinn S, Hawkins KC, Ericson K, Terracio L, Moreau C, Hixson D, Tobin BW, Hudson J, Bowyer FP 3rd, Black AC Jr. Young HE, et al. Anat Rec A Discov Mol Cell Evol Biol. 2004 Mar;277(1):178-203. doi: 10.1002/ar.a.20000. Anat Rec A Discov Mol Cell Evol Biol. 2004. PMID: 14983513
  • Clonogenic analysis reveals reserve stem cells in postnatal mammals: I. Pluripotent mesenchymal stem cells.
    Young HE, Duplaa C, Young TM, Floyd JA, Reeves ML, Davis KH, Mancini GJ, Eaton ME, Hill JD, Thomas K, Austin T, Edwards C, Cuzzourt J, Parikh A, Groom J, Hudson J, Black AC Jr. Young HE, et al. Anat Rec. 2001 Aug 1;263(4):350-60. doi: 10.1002/ar.1112. Anat Rec. 2001. PMID: 11500811
  • Karyotypic analysis of adult pluripotent stem cells.
    Henson NL, Heaton ML, Holland BH, Hawkins KC, Rawlings BA, Eanes EA, Bozof RG, Powell SW, Grau RE, Fortney JA, Peebles BG, Kumar D, Yoon JI, Godby KN, Collins JA, Sood R, Hixson D, Bowyer FP 3rd, Black AC Jr, Young HE. Henson NL, et al. Histol Histopathol. 2005 Jul;20(3):769-84. doi: 10.14670/HH-20.769. Histol Histopathol. 2005. PMID: 15944926

Cited by

Publication types

LinkOut - more resources