Resting and activated subsets of mouse multipotent hematopoietic stem cells
- PMID: 1977160
- PMCID: PMC54761
- DOI: 10.1073/pnas.87.19.7433
Resting and activated subsets of mouse multipotent hematopoietic stem cells
Abstract
The fluorescent vital dye rhodamine 123 (Rh-123), which preferentially accumulates in mitochondrial membranes, can be used as a probe to indicate mitochondrial and hence cellular activity. In this study, mouse bone marrow hematopoietic stem cells were subdivided into Rh-123lo, Rh-123med, and Rh-123hi populations. The Rh-123lo (resting) population was significantly enriched in cells with a higher proliferative potential compared to the Rh-123hi (activated) population. The resting population exhibited a 20-fold greater ability to differentiate into splenic colony-forming units (CFU-S) relative to the activated population, whereas the activated population contained about 4-fold more day 13 CFU-S on primary transfer relative to the resting population. The two populations produced morphologically distinct splenic colonies; however, the frequency and morphology of in vitro colonies were very similar. Only the resting population provided sufficient stem cells to transfer long-term hematopoietic repopulation to secondary recipient animals after lethal irradiation. On a single cell level, the resting and activated populations exhibited an equivalent ability to differentiate into lymphoid and myeloid progeny. These observations provide further insight into the heterogeneous nature of CFU-S and directly demonstrate that multipotent hematopoietic stem cells are heterogeneous with regard to their clonogenic capacities.
Similar articles
-
In vivo and in vitro characterization of long-term repopulating primitive hematopoietic cells isolated by sequential Hoechst 33342-rhodamine 123 FACS selection.Exp Hematol. 1993 May;21(5):614-22. Exp Hematol. 1993. PMID: 8513861
-
Separation and functional analysis of bone marrow cells separated by rhodamine-123 fluorescence.Exp Hematol. 1987 Jan;15(1):99-104. Exp Hematol. 1987. PMID: 3536548
-
Long-term repopulation of irradiated mice with limiting numbers of purified hematopoietic stem cells: in vivo expansion of stem cell phenotype but not function.Blood. 1995 Feb 15;85(4):1006-16. Blood. 1995. PMID: 7849289
-
Multiparameter analysis of transplantable hemopoietic stem cells: I. The separation and enrichment of stem cells homing to marrow and spleen on the basis of rhodamine-123 fluorescence.Exp Hematol. 1985 Nov;13(10):999-1006. Exp Hematol. 1985. PMID: 2865163
-
Spleen colony-forming unit: a myeloid stem cell.Curr Top Microbiol Immunol. 1992;177:75-82. doi: 10.1007/978-3-642-76912-2_6. Curr Top Microbiol Immunol. 1992. PMID: 1638872 Review. No abstract available.
Cited by
-
The hematopoietic stem compartment consists of a limited number of discrete stem cell subsets.Blood. 2006 Mar 15;107(6):2311-6. doi: 10.1182/blood-2005-07-2970. Epub 2005 Nov 15. Blood. 2006. PMID: 16291588 Free PMC article.
-
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo.J Exp Med. 1996 Apr 1;183(4):1797-806. doi: 10.1084/jem.183.4.1797. J Exp Med. 1996. PMID: 8666936 Free PMC article.
-
Stem cells from birth to death: The history and the future.J Am Aging Assoc. 2002 Apr;25(2):79-86. doi: 10.1007/s11357-002-0006-z. J Am Aging Assoc. 2002. PMID: 23604899 Free PMC article.
-
Developmental potential of the earliest precursor cells from the adult mouse thymus.J Exp Med. 1991 Dec 1;174(6):1617-27. doi: 10.1084/jem.174.6.1617. J Exp Med. 1991. PMID: 1683894 Free PMC article.
-
Genetic control of murine hematopoietic stem cell pool sizes and cycling kinetics.Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11607-11. doi: 10.1073/pnas.89.23.11607. Proc Natl Acad Sci U S A. 1992. PMID: 1280831 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical