A Quadripotential Mesenchymal Progenitor Cell Isolated from the Marrow of an Adult Mouse

Adult marrow contains mesenchymal progenitor cells (MPCs) that have multiple differentiation potentials. A conditionally immortalized MPC clone, BMC9, has been identified that exhibits four mesenchymal cell phenotypes: chondrocyte, adipocyte, stromal (support osteoclast formation), and osteoblast. The BMC9 clone, control brain fibroblasts and another marrow‐derived clone, BMC10, were isolated from a transgenic mouse (H‐2Kb‐tsA58) containing a gene for conditional immortality. To test for chondrogenic potential, cells were cultured in defined medium containing 10 ng/ml transforming growth factor β and 10−7 M dexamethasone in 15‐ml polypropylene tubes (“aggregate cultures”). Adipogenic potential was quantitated by flow cytometry of Nile Red–stained cells cultured for 1 and 2 weeks in medium containing isobutyl methylxanthine, indomethacin, insulin, and dexamethasone. Support of osteoclast formation was measured by quantitating multinucleated tartrate‐resistant acid phosphatase–positive cells in spleen cell cocultures of test clones (immortomouse clones and positive control ST2 cells) cultured in the presence of 10−7 M vitamin D3 and 150 mM ascorbate‐2‐phosphate. In vivo osteogenic potential was assayed by histologic examination of bone formation in subcutaneous implants, into athymic mouse hosts, of a composite of cells combined with porous calcium phosphate ceramics. The bone marrow–derived clone BMC9 has the potential to express each of the four mesenchymal characteristics tested, while brain fibroblasts, tested under identical conditions, did not exhibit any of these four mesenchymal characteristics. BMC10 cells exhibited osteogenic and chondrogenic phenotypes, but showed only minimal expression of adipocytic or osteoclast‐supportive phenotypes. Clone BMC9 is, minimally, a quadripotential MPC isolated from the marrow of an adult mouse that can differentiate into cartilage and adipose, support osteoclast formation, and form bone. The BMC9 clone is an example of an adult‐derived multipotential progenitor cell that is situated early in the mesenchymal lineage.

[1]  A. Caplan,et al.  In vivo osteogenesis assay: a rapid method for quantitative analysis. , 1998, Biomaterials.

[2]  R. Baron,et al.  Murine bone marrow stromally derived BMS2 adipocytes support differentiation and function of osteoclast-like cells in vitro. , 1998, Endocrinology.

[3]  M. Nuttall,et al.  Human Trabecular Bone Cells Are Able to Express Both Osteoblastic and Adipocytic Phenotype: Implications for Osteopenic Disorders , 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[4]  A I Caplan,et al.  In vitro chondrogenesis of bone marrow-derived mesenchymal progenitor cells. , 1998, Experimental cell research.

[5]  D. Benayahu,et al.  Single‐Colony Derived Strains of Human Marrow Stromal Fibroblasts Form Bone After Transplantation In Vivo , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[6]  S. Wientroub,et al.  Osteocalcin (BGP), gene expression, and protein production by marrow stromal adipocytes. , 1997, Biochemical and biophysical research communications.

[7]  S. Bruder,et al.  Osteogenic differentiation of purified, culture‐expanded human mesenchymal stem cells in vitro , 1997, Journal of cellular biochemistry.

[8]  F. Ross,et al.  Estrogen Deficiency Increases the Ability of Stromal Cells to Support Murine Osteoclastogenesis via an Interleukin-1and Tumor Necrosis Factor-mediated Stimulation of Macrophage Colony-stimulating Factor Production* , 1996, The Journal of Biological Chemistry.

[9]  T. Katagiri,et al.  Subcloning of three osteoblastic cell lines with distinct differentiation phenotypes from the mouse osteoblastic cell line KS-4. , 1996, Bone.

[10]  A. Caplan,et al.  Differentiation potential of conditionally immortalized mesenchymal progenitor cells from adult marrow of a H‐2Kb‐tsA58 transgenic mouse , 1996, Journal of cellular physiology.

[11]  A. Caplan,et al.  Myogenic Expression of Mesenchymal Stem Cells within Myotubes of mdx Mice in Vitro and in Vivo. , 1995, Tissue engineering.

[12]  A. Caplan,et al.  Myogenic cells derived from rat bone marrow mesenchymal stem cells exposed to 5‐azacytidine , 1995, Muscle & nerve.

[13]  D. Benayahu,et al.  Myeloblastic cell line expresses osteoclastic properties following coculture with marrow stromal adipocytes , 1994, Journal of cellular biochemistry.

[14]  B. Ratnikov,et al.  Clonal analysis of primary marrow stroma: functional homogeneity in support of lymphoid and myeloid cell lines and identification of positive and negative regulators. , 1994, Experimental hematology.

[15]  L. Frantsve,et al.  Cytokine production and heterogeneity of primary stromal cells that support B lymphopoiesis , 1993, European journal of immunology.

[16]  J. Falkenburg,et al.  Regulation of myelopoiesis by murine fibroblastic and adipogenic cell lines. , 1993, Experimental hematology.

[17]  W. Wharton,et al.  Multiparameter flow cytometric analysis of the effects of indomethacin on adipocyte differentiation in A31T6 cells , 1993, Cell proliferation.

[18]  J. Gimble,et al.  Osteoblastic gene expression during adipogenesis in hematopoietic supporting murine bone marrow stromal cells , 1993, Journal of cellular physiology.

[19]  J. Greenberger,et al.  Adipogenesis in a myeloid supporting bone marrow stromal cell line , 1992, Journal of cellular biochemistry.

[20]  P. Witte,et al.  Enrichment of primary lymphocyte‐supporting stromal cells and characterization of associated B lymphocyte progenitors , 1992, European journal of immunology.

[21]  W. Wharton,et al.  Differentiation of A31T6 proadipocytes to adipocytes: a flow cytometric analysis. , 1992, Experimental cell research.

[22]  T. Martin,et al.  Modulation of osteoclast differentiation. , 1992, Endocrine reviews.

[23]  A. Caplan,et al.  Osteogenesis in Marrow-Derived Mesenchymal Cell Porous Ceramic Composites Transplanted Subcutaneously: Effect of Fibronectin and Laminin on Cell Retention and Rate of Osteogenic Expression , 1992, Cell transplantation.

[24]  D. Kioussis,et al.  Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Triffitt,et al.  Adipocytic cells cultured from marrow have osteogenic potential. , 1991, Journal of cell science.

[26]  T. Martin,et al.  The bone marrow-derived stromal cell lines MC3T3-G2/PA6 and ST2 support osteoclast-like cell differentiation in cocultures with mouse spleen cells. , 1989, Endocrinology.

[27]  V. Goldberg,et al.  Heterotopic osteogenesis in porous ceramics induced by marrow cells , 1989, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[28]  S. Wientroub,et al.  Bone marrow‐derived stromal cell line expressing osteoblastic phenotype in vitro and osteogenic capacity in vivo , 1989, Journal of cellular physiology.

[29]  A I Caplan,et al.  Repair of bone defects with marrow cells and porous ceramic. Experiments in rats. , 1989, Acta orthopaedica Scandinavica.

[30]  P. Kincade,et al.  Stromal cell lines which support lymphocyte growth: characterization, sensitivity to radiation and responsiveness to growth factors , 1988, European journal of immunology.

[31]  C. R. Howlett,et al.  Ultrastructure of bone and cartilage formed in vivo in diffusion chambers. , 1984, Clinical orthopaedics and related research.

[32]  L. Kearney,et al.  Effects of human marrow stromal cells on proliferation by human granulocytic (GM‐CFC), erythroid (BFU‐E) and mixed (Mix‐CFC) colony‐forming cells , 1983, British journal of haematology.

[33]  R. Salter,et al.  The biological effect of continuous passive motion on the healing of full-thickness defects in articular cartilage. An experimental investigation in the rabbit. , 1980, The Journal of bone and joint surgery. American volume.

[34]  C. R. Howlett,et al.  Formation of bone and cartilage by marrow stromal cells in diffusion chambers in vivo. , 1980, Clinical orthopaedics and related research.

[35]  L. Lajtha,et al.  Conditions controlling the proliferation of haemopoietic stem cells in vitro , 1977, Journal of cellular physiology.

[36]  F. N. Ghadially,et al.  Long‐term results of superficial defects in articular cartilage: A scanning electronmicroscope study , 1977, The Journal of pathology.

[37]  N. Kulagina,et al.  Fibroblast precursors in normal and irradiated mouse hematopoietic organs. , 1976, Experimental hematology.

[38]  N Mitchell,et al.  The resurfacing of adult rabbit articular cartilage by multiple perforations through the subchondral bone. , 1976, The Journal of bone and joint surgery. American volume.

[39]  D. G. Walker Control of bone resorption by hematopoietic tissue. The induction and reversal of congenital osteopetrosis in mice through use of bone marrow and splenic transplants , 1975, The Journal of experimental medicine.

[40]  A. Friedenstein,et al.  STROMAL CELLS RESPONSIBLE FOR TRANSFERRING THE MICROENVIRONMENT OF THE HEMOPOIETIC TISSUES: Cloning In Vitro and Retransplantation In Vivo , 1974, Transplantation.

[41]  M. Tavassoli,et al.  The Effects of Phenylhydrazine‐Induced Haemolysis on the Behaviour of Regenerating Marrow Stroma , 1972, British journal of haematology.

[42]  F. N. Ghadially,et al.  Ultrastructural observations on surgically produced partial-thickness defects in articular cartilage. , 1972, Clinical orthopaedics and related research.

[43]  W. Akeson,et al.  The Repair of Large Osteochondral Defects An Experimental Study in Horses , 1972, Clinical orthopaedics and related research.

[44]  M. Tavassoli,et al.  Factors affecting the conversion of yellow to red marrow. , 1971, Blood.

[45]  A. Friedenstein,et al.  Heterotopic of bone marrow. Analysis of precursor cells for osteogenic and hematopoietic tissues. , 1968, Transplantation.

[46]  A. Friedenstein,et al.  Osteogenesis in transplants of bone marrow cells. , 1966, Journal of embryology and experimental morphology.

[47]  Depalma Af,et al.  Process of repair of articular cartilage demonstrated by histology and autoradiography with tritiated thymidine. , 1966 .

[48]  A. A. Tolmacheva,et al.  [BONE FORMATION OCCURRING IN BONE MARROW TRANSPLANTATION IN DIFFUSION CHAMBERS]. , 1963, Biulleten' eksperimental'noi biologii i meditsiny.

[49]  G. Meachim THE EFFECT OF SCARIFICATION ON ARTICULAR CARTILAGE IN THE RABBIT , 1963 .

[50]  C. Skinner The Biochemistry and Physiology of Bone , 1956, The Yale Journal of Biology and Medicine.

[51]  A. Caplan,et al.  Analysis of the developmental potential of conditionally immortal marrow-derived mesenchymal progenitor cells isolated from the H-2Kb-tsA58 transgenic mouse. , 1996, Connective tissue research.

[52]  G. Wang,et al.  Induction of the , 1996 .

[53]  M. Katoh,et al.  Induction of bone resorbing-activity by mouse stromal cell line, MC3T3-G2/PA6. , 1995, Bone.

[54]  J. Dennis Mesenchymal progenitor cells in adult marrow. , 1995 .

[55]  A. Caplan,et al.  Porous ceramic vehicles for rat-marrow-derived (Rattus norvegicus) osteogenic cell delivery: effects of pre-treatment with fibronectin or laminin. , 1993, The Journal of oral implantology.

[56]  E. Deryugina,et al.  Stromal cells in long-term cultures: keys to the elucidation of hematopoietic development? , 1993, Critical reviews in immunology.

[57]  A I Caplan,et al.  Characterization of cells with osteogenic potential from human marrow. , 1992, Bone.

[58]  D. Kioussis,et al.  H‐2Kb‐tsA58トランスジェニックマウスから直接に無限増殖細胞系を得る方法 , 1991 .

[59]  A I Caplan,et al.  The osteogenic potential of culture-expanded rat marrow mesenchymal cells assayed in vivo in calcium phosphate ceramic blocks. , 1991, Clinical orthopaedics and related research.

[60]  T. Dexter,et al.  Culturing Primitive Hemopoietic Cells : Long-Term Mouse Marrow Cultures and the Establishment of Factor-Dependent (FDCP-Mix) Hemopoietic Cell Lines. , 1990, Methods in molecular biology.

[61]  A. Friedenstein,et al.  Stromal stem cells: marrow-derived osteogenic precursors. , 1988, Ciba Foundation symposium.

[62]  A. Friedenstein,et al.  Marrow microenvironment transfer by heterotopic transplantation of freshly isolated and cultured cells in porous sponges. , 1982, Experimental hematology.

[63]  F. N. Ghadially,et al.  Long-term results of superficial defects in articular cartilage: a scanning electron-microscope study. , 1977, The Journal of pathology.

[64]  M. Tavassoli Marrow adipose cells. Histochemical identification of labile and stable components. , 1976, Archives of pathology & laboratory medicine.

[65]  A. Depalma,et al.  Process of repair of articular cartilage demonstrated by histology and autoradiography with tritiated thymidine. , 1966, Clinical orthopaedics and related research.

[66]  A. Ham,et al.  REPAIR AND TRANSPLANTATION OF BONE , 1956 .