Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain

Yuehua Jiang, Ben Vaessen, Todd Lenvik, Mark Blackstad, Morayma Reyes Gil, Catherine M. Verfaillie

Research output: Contribution to journalArticle

724 Citations (Scopus)

Abstract

Objective: Recent studies have shown that cells from bone marrow (BM), muscle, and brain may have greater plasticity than previously known. We have identified multipotent adult progenitor cells (MAPC) in postnatal human and rodent BM that copurify with mesenchymal stem cells (MSC). BM MAPC proliferate without senescence and differentiate into mesodermal, neuroectodermal, and endodermal cell types. We hypothesized that cells with characteristics similar to BM MAPC can be selected and cultured from tissues other than BM. Materials and Methods: BM, whole brain, and whole muscle tissue was obtained from mice. Cells were plated on Dulbecco modified Eagle medium supplemented with 2% fetal calf serum and 10 ng/mL epidermal growth factor (EGF), 10 ng/mL platelet-derived growth factor (PDGF-BB), and 1000 units/mL leukemia inhibitory factor (LIF) for more than 6 months. Cells were maintained between 0.5 and 1.5 × 103 cells/cm2. At variable time points, we tested cell phenotype by FACS and evaluated their differentiation into endothelial cells, neuroectodermal cells, and endodermal cells in vitro. We also compared the expressed gene profile in BM, muscle, and brain MAPC by Affimetrix gene array analysis. Results: Cells could be cultured from BM, muscle, and brain that proliferated for more than 70 population doublings (PDs) and were negative for CD44, CD45, major histocompatibility complex class I and II, and c-kit. Cells from the three tissues differentiated to cells with morphologic and phenotypic characteristics of endothelium, neurons, glia, and hepatocytes. The expressed gene profile of cells derived from the three tissues was identical (r2 > 0.975). Conclusions: This study shows that cells with MAPC characteristics can be isolated not only from BM, but also from brain and muscle tissue. Whether MAPC originally derived from BM are circulating or all organs contain stem cells with MAPC characteristics currently is being studied. Presence of MAPC in multiple tissues may help explain the 'plasticity' found in multiple adult tissues.

Original languageEnglish (US)
Pages (from-to)896-904
Number of pages9
JournalExperimental Hematology
Volume30
Issue number8
DOIs
StatePublished - 2002
Externally publishedYes

Fingerprint

Stem Cells
Bone Marrow
Muscles
Brain
Multipotent Stem Cells
Genes
Leukemia Inhibitory Factor
Eagles
Major Histocompatibility Complex
Mesenchymal Stromal Cells
Epidermal Growth Factor
Neuroglia
Bone Marrow Cells
Endothelium
Hepatocytes
Rodentia
Endothelial Cells
Phenotype
Neurons

ASJC Scopus subject areas

  • Cancer Research
  • Cell Biology
  • Genetics
  • Hematology
  • Oncology
  • Transplantation

Cite this

Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain. / Jiang, Yuehua; Vaessen, Ben; Lenvik, Todd; Blackstad, Mark; Reyes Gil, Morayma; Verfaillie, Catherine M.

In: Experimental Hematology, Vol. 30, No. 8, 2002, p. 896-904.

Research output: Contribution to journalArticle

Jiang, Yuehua ; Vaessen, Ben ; Lenvik, Todd ; Blackstad, Mark ; Reyes Gil, Morayma ; Verfaillie, Catherine M. / Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain. In: Experimental Hematology. 2002 ; Vol. 30, No. 8. pp. 896-904.
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abstract = "Objective: Recent studies have shown that cells from bone marrow (BM), muscle, and brain may have greater plasticity than previously known. We have identified multipotent adult progenitor cells (MAPC) in postnatal human and rodent BM that copurify with mesenchymal stem cells (MSC). BM MAPC proliferate without senescence and differentiate into mesodermal, neuroectodermal, and endodermal cell types. We hypothesized that cells with characteristics similar to BM MAPC can be selected and cultured from tissues other than BM. Materials and Methods: BM, whole brain, and whole muscle tissue was obtained from mice. Cells were plated on Dulbecco modified Eagle medium supplemented with 2{\%} fetal calf serum and 10 ng/mL epidermal growth factor (EGF), 10 ng/mL platelet-derived growth factor (PDGF-BB), and 1000 units/mL leukemia inhibitory factor (LIF) for more than 6 months. Cells were maintained between 0.5 and 1.5 × 103 cells/cm2. At variable time points, we tested cell phenotype by FACS and evaluated their differentiation into endothelial cells, neuroectodermal cells, and endodermal cells in vitro. We also compared the expressed gene profile in BM, muscle, and brain MAPC by Affimetrix gene array analysis. Results: Cells could be cultured from BM, muscle, and brain that proliferated for more than 70 population doublings (PDs) and were negative for CD44, CD45, major histocompatibility complex class I and II, and c-kit. Cells from the three tissues differentiated to cells with morphologic and phenotypic characteristics of endothelium, neurons, glia, and hepatocytes. The expressed gene profile of cells derived from the three tissues was identical (r2 > 0.975). Conclusions: This study shows that cells with MAPC characteristics can be isolated not only from BM, but also from brain and muscle tissue. Whether MAPC originally derived from BM are circulating or all organs contain stem cells with MAPC characteristics currently is being studied. Presence of MAPC in multiple tissues may help explain the 'plasticity' found in multiple adult tissues.",
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T1 - Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain

AU - Jiang, Yuehua

AU - Vaessen, Ben

AU - Lenvik, Todd

AU - Blackstad, Mark

AU - Reyes Gil, Morayma

AU - Verfaillie, Catherine M.

PY - 2002

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