Skip to main content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
J Cell Biol. 1988 Jun 1; 106(6): 2139–2151.
PMCID: PMC2115137
PMID: 3384856

Differentiation of muscle, fat, cartilage, and bone from progenitor cells present in a bone-derived clonal cell population: effect of dexamethasone

Abstract

RCJ 3.1, a clonally derived cell population isolated from 21-d fetal rat calvaria, expresses the osteoblast-associated characteristics of polygonal morphology, a cAMP response to parathyroid hormone, synthesis of predominantly type I collagen, and the presence of 1,25- dihydroxyvitamin D3-regulated alkaline phosphatase activity. When cultured in the presence of ascorbic acid, sodium beta- glycerophosphate, and the synthetic glucocorticoid dexamethasone, this clone differentiated in a time-dependent manner into four morphologically distinct phenotypes of known mesenchymal origin. Multinucleated muscle cells were observed as early as 9-10 d in culture, lipid-containing adipocytes formed after 12 d, chondrocyte nodules were observed after 16 d, and mineralized bone nodules formed after 21 d in culture. The differentiated cell types were characterized morphologically, histochemically, and immunohistochemically. The formation of adipocytes and chondrocytes was dependent upon the addition of dexamethasone; the muscle and bone phenotypes were also expressed at low frequency in the absence of dexamethasone. The sex steroid hormones progesterone and 17 beta-estradiol had no effect on differentiation in this system, suggesting that the effects of dexamethasone represent effects specific for glucocorticosteroids. Increasing concentrations of dexamethasone (10(-9)-10(-6) M) increased the numbers of myotubes, adipocytes, and chondrocytes; however, when present continuously for 35 d, the lower concentrations appeared to better maintain the muscle and adipocyte phenotypes. Bone nodules were not quantitated because the frequency of bone nodule formation was too low. Single cells obtained by plating RCJ 3.1 cells at limiting dilutions in the presence of dexamethasone, were shown to give rise to subclones that could differentiate into either single or multiple phenotypes. Thus, the data suggest that this clonal cell line contains subpopulations of mesenchymal progenitor cells which can, under the influence of glucocorticoid hormones, differentiate in vitro into four distinct cell types. It is, therefore, a unique cell line which will be of great use in the study of the regulation of mesenchymal stem cell differentiation.

Full Text

The Full Text of this article is available as a PDF (4.5M).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  • Allen RE, Dodson MV, Luiten LS, Boxhorn LK. A serum-free medium that supports the growth of cultured skeletal muscle satellite cells. In Vitro Cell Dev Biol. 1985 Nov;21(11):636–640. [PubMed] [Google Scholar]
  • Antosz ME, Bellows CG, Aubin JE. Biphasic effects of epidermal growth factor on bone nodule formation by isolated rat calvaria cells in vitro. J Bone Miner Res. 1987 Oct;2(5):385–393. [PubMed] [Google Scholar]
  • Aubin JE, Alders E, Heersche JN. A primary role for microfilaments, but not microtubules, in hormone-induced cytoplasmic retraction. Exp Cell Res. 1983 Feb;143(2):439–450. [PubMed] [Google Scholar]
  • Aubin JE, Heersche JN, Merrilees MJ, Sodek J. Isolation of bone cell clones with differences in growth, hormone responses, and extracellular matrix production. J Cell Biol. 1982 Feb;92(2):452–461. [PMC free article] [PubMed] [Google Scholar]
  • Ball EH, Sanwal BD. A synergistic effect of glucocorticoids and insulin on the differentiation of myoblasts. J Cell Physiol. 1980 Jan;102(1):27–36. [PubMed] [Google Scholar]
  • Bellows CG, Aubin JE, Heersche JN. Physiological concentrations of glucocorticoids stimulate formation of bone nodules from isolated rat calvaria cells in vitro. Endocrinology. 1987 Dec;121(6):1985–1992. [PubMed] [Google Scholar]
  • Bellows CG, Aubin JE, Heersche JN, Antosz ME. Mineralized bone nodules formed in vitro from enzymatically released rat calvaria cell populations. Calcif Tissue Int. 1986 Mar;38(3):143–154. [PubMed] [Google Scholar]
  • Bellows CG, Sodek J, Yao KL, Aubin JE. Phenotypic differences in subclones and long-term cultures of clonally derived rat bone cell lines. J Cell Biochem. 1986;31(2):153–169. [PubMed] [Google Scholar]
  • Caplan AI. The effects of the nicotinamide sensitive teratogen 3-acetylpyridine on chick limb mesodermal cells in culture: biochemical parameters. J Exp Zool. 1972 Jun;180(3):351–362. [PubMed] [Google Scholar]
  • Caplan AI, Stoolmiller AC. Control of chondrogenic expression in mesodermal cells of embryonic chick limb. Proc Natl Acad Sci U S A. 1973 Jun;70(6):1713–1717. [PMC free article] [PubMed] [Google Scholar]
  • Chapman AB, Knight DM, Dieckmann BS, Ringold GM. Analysis of gene expression during differentiation of adipogenic cells in culture and hormonal control of the developmental program. J Biol Chem. 1984 Dec 25;259(24):15548–15555. [PubMed] [Google Scholar]
  • Chyun YS, Raisz LG. Stimulation of bone formation by prostaglandin E2. Prostaglandins. 1984 Jan;27(1):97–103. [PubMed] [Google Scholar]
  • Constantinides PG, Jones PA, Gevers W. Functional striated muscle cells from non-myoblast precursors following 5-azacytidine treatment. Nature. 1977 May 26;267(5609):364–366. [PubMed] [Google Scholar]
  • Debus E, Weber K, Osborn M. Monoclonal antibodies to desmin, the muscle-specific intermediate filament protein. EMBO J. 1983;2(12):2305–2312. [PMC free article] [PubMed] [Google Scholar]
  • Delaporte C, Dautreaux B, Fardeau M. Human myotube differentiation in vitro in different culture conditions. Biol Cell. 1986;57(1):17–22. [PubMed] [Google Scholar]
  • Florini JR, Roberts AB, Ewton DZ, Falen SL, Flanders KC, Sporn MB. Transforming growth factor-beta. A very potent inhibitor of myoblast differentiation, identical to the differentiation inhibitor secreted by Buffalo rat liver cells. J Biol Chem. 1986 Dec 15;261(35):16509–16513. [PubMed] [Google Scholar]
  • Foster SJ, Perkins JP. Glucocorticoids increase the responsiveness of cells in culture to prostaglandin E1. Proc Natl Acad Sci U S A. 1977 Nov;74(11):4816–4820. [PMC free article] [PubMed] [Google Scholar]
  • Gospodarowicz D, Weseman J, Moran JS, Lindstrom J. Effect of fibroblast growth factor on the division and fusion of bovine myoblasts. J Cell Biol. 1976 Aug;70(2 Pt 1):395–405. [PMC free article] [PubMed] [Google Scholar]
  • Green H, Kehinde O. Spontaneous heritable changes leading to increased adipose conversion in 3T3 cells. Cell. 1976 Jan;7(1):105–113. [PubMed] [Google Scholar]
  • Green H, Morikawa M, Nixon T. A dual effector theory of growth-hormone action. Differentiation. 1985;29(3):195–198. [PubMed] [Google Scholar]
  • Grigoriadis AE, Petkovich PM, Rosenthal EE, Heersche JN. Modulation by retinoic acid of 1,25-dihydroxyvitamin D3 effects on alkaline phosphatase activity and parathyroid hormone responsiveness in an osteoblast-like osteosarcoma cell line. Endocrinology. 1986 Aug;119(2):932–939. [PubMed] [Google Scholar]
  • Guerriero V, Jr, Florini JR. Dexamethasone effects on myoblast proliferation and differentiation. Endocrinology. 1980 Apr;106(4):1198–1202. [PubMed] [Google Scholar]
  • Hauschka SD, Konigsberg IR. The influence of collagen on the development of muscle clones. Proc Natl Acad Sci U S A. 1966 Jan;55(1):119–126. [PMC free article] [PubMed] [Google Scholar]
  • Ignotz RA, Massagué J. Type beta transforming growth factor controls the adipogenic differentiation of 3T3 fibroblasts. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8530–8534. [PMC free article] [PubMed] [Google Scholar]
  • Kato Y, Gospodarowicz D. Stimulation by glucocorticoid of the synthesis of cartilage-matrix proteoglycans produced by rabbit costal chondrocytes in vitro. J Biol Chem. 1985 Feb 25;260(4):2364–2373. [PubMed] [Google Scholar]
  • Kleinman HK, Klebe RJ, Martin GR. Role of collagenous matrices in the adhesion and growth of cells. J Cell Biol. 1981 Mar;88(3):473–485. [PMC free article] [PubMed] [Google Scholar]
  • Kodama HA, Amagai Y, Koyama H, Kasai S. Hormonal responsiveness of a preadipose cell line derived from newborn mouse calvaria. J Cell Physiol. 1982 Jul;112(1):83–88. [PubMed] [Google Scholar]
  • Kuri-Harcuch W. Differentiation of 3T3-F442A cells into adipocytes is inhibited by retinoic acid. Differentiation. 1982;23(2):164–169. [PubMed] [Google Scholar]
  • Lathrop B, Olson E, Glaser L. Control by fibroblast growth factor of differentiation in the BC3H1 muscle cell line. J Cell Biol. 1985 May;100(5):1540–1547. [PMC free article] [PubMed] [Google Scholar]
  • Leibovitch SA, Hillion J, Leibovitch MP, Guillier M, Schmitz A, Harel J. Expression of extracellular matrix genes in relation to myogenesis and neoplastic transformation. Exp Cell Res. 1986 Oct;166(2):526–534. [PubMed] [Google Scholar]
  • Limeback HF, Sodek J. Procollagen synthesis and processing in periodontal ligament in vivo and in vitro. A comparative study using slab-gel fluorography. Eur J Biochem. 1979 Oct 15;100(2):541–550. [PubMed] [Google Scholar]
  • Linkhart TA, Clegg CH, Hauschika SD. Myogenic differentiation in permanent clonal mouse myoblast cell lines: regulation by macromolecular growth factors in the culture medium. Dev Biol. 1981 Aug;86(1):19–30. [PubMed] [Google Scholar]
  • Maor G, Silbermann M. Supraphysiological concentrations of dexamethasone induce elevation of calcium uptake and depression of [3H]-thymidine incorporation into DNA in cartilage in vitro. Calcif Tissue Int. 1986 Oct;39(4):284–290. [PubMed] [Google Scholar]
  • Massagué J, Cheifetz S, Endo T, Nadal-Ginard B. Type beta transforming growth factor is an inhibitor of myogenic differentiation. Proc Natl Acad Sci U S A. 1986 Nov;83(21):8206–8210. [PMC free article] [PubMed] [Google Scholar]
  • Nefussi JR, Boy-Lefevre ML, Boulekbache H, Forest N. Mineralization in vitro of matrix formed by osteoblasts isolated by collagenase digestion. Differentiation. 1985;29(2):160–168. [PubMed] [Google Scholar]
  • Négrel R, Grimaldi P, Ailhaud G. Establishment of preadipocyte clonal line from epididymal fat pad of ob/ob mouse that responds to insulin and to lipolytic hormones. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6054–6058. [PMC free article] [PubMed] [Google Scholar]
  • Nixon BT, Green H. Growth hormone promotes the differentiation of myoblasts and preadipocytes generated by azacytidine treatment of 10T1/2 cells. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3429–3432. [PMC free article] [PubMed] [Google Scholar]
  • Olson EN, Sternberg E, Hu JS, Spizz G, Wilcox C. Regulation of myogenic differentiation by type beta transforming growth factor. J Cell Biol. 1986 Nov;103(5):1799–1805. [PMC free article] [PubMed] [Google Scholar]
  • Osdoby P, Caplan AI. The possible differentiation of osteogenic elements in vitro from chick limb mesodermal cells. I. Morphological evidence. Dev Biol. 1976 Sep;52(2):283–299. [PubMed] [Google Scholar]
  • Osdoby P, Caplan AI. Osteogenesis in cultures of limb mesenchymal cells. Dev Biol. 1979 Nov;73(1):84–102. [PubMed] [Google Scholar]
  • Ravdin P, Axelrod D. Fluorescent tetramethyl rhodamine derivatives of alpha-bungarotoxin: preparation, separation, and characterization. Anal Biochem. 1977 Jun;80(2):585–592. [PubMed] [Google Scholar]
  • Reddi AH, Huggins C. Biochemical sequences in the transformation of normal fibroblasts in adolescent rats. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1601–1605. [PMC free article] [PubMed] [Google Scholar]
  • Reznikoff CA, Brankow DW, Heidelberger C. Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division. Cancer Res. 1973 Dec;33(12):3231–3238. [PubMed] [Google Scholar]
  • Ringold GM, Chapman AB, Knight DM. Glucocorticoid control of developmentally regulated adipose genes. J Steroid Biochem. 1986 Jan;24(1):69–75. [PubMed] [Google Scholar]
  • Rubin CS, Hirsch A, Fung C, Rosen OM. Development of hormone receptors and hormonal responsiveness in vitro. Insulin receptors and insulin sensitivity in the preadipocyte and adipocyte forms of 3T3-L1 cells. J Biol Chem. 1978 Oct 25;253(20):7570–7578. [PubMed] [Google Scholar]
  • Rubin CS, Lai E, Rosen OM. Acquisition of increased hormone sensitivity during in vitro adipocyte development. J Biol Chem. 1977 May 25;252(10):3554–3557. [PubMed] [Google Scholar]
  • Schiwek DR, Löffler G. Glucocorticoid hormones contribute to the adipogenic activity of human serum. Endocrinology. 1987 Feb;120(2):469–474. [PubMed] [Google Scholar]
  • Scott-Burden T, Bogenmann E, Jones PA. Effects of complex extracellular matrices on 5-azacytidine-induced myogenesis. Exp Cell Res. 1986 Jun;164(2):527–535. [PubMed] [Google Scholar]
  • Shimizu M, Torti F, Roth RA. Characterization of the insulin and insulin-like growth factor receptors and responsitivity of a fibroblast/adipocyte cell line before and after differentiation. Biochem Biophys Res Commun. 1986 May 29;137(1):552–558. [PubMed] [Google Scholar]
  • Smith TJ, Dana R, Krichevsky A, Bilezikian JP, Schonberg M. Inhibition of beta-adrenergic responsiveness in muscle cell cultures by dexamethasone. Endocrinology. 1981 Dec;109(6):2110–2116. [PubMed] [Google Scholar]
  • Sparks RL, Scott RE. Transforming growth factor type beta is a specific inhibitor of 3T3 T mesenchymal stem cell differentiation. Exp Cell Res. 1986 Aug;165(2):345–352. [PubMed] [Google Scholar]
  • Spiegelman BM, Ginty CA. Fibronectin modulation of cell shape and lipogenic gene expression in 3T3-adipocytes. Cell. 1983 Dec;35(3 Pt 2):657–666. [PubMed] [Google Scholar]
  • Spizz G, Roman D, Strauss A, Olson EN. Serum and fibroblast growth factor inhibit myogenic differentiation through a mechanism dependent on protein synthesis and independent of cell proliferation. J Biol Chem. 1986 Jul 15;261(20):9483–9488. [PubMed] [Google Scholar]
  • Steinberg MM, Brownstein BL. A clonal analysis of the differentiation of 3T3-L1 preadipose cells: role of insulin. J Cell Physiol. 1982 Dec;113(3):359–364. [PubMed] [Google Scholar]
  • Takano T, Takigawa M, Suzuki F. Stimulation by glucocorticoids of the differentiated phenotype of chondrocytes and the proliferation of rabbit costal chondrocytes in culture. J Biochem. 1985 Apr;97(4):1093–1100. [PubMed] [Google Scholar]
  • Taylor SM, Jones PA. Multiple new phenotypes induced in 10T1/2 and 3T3 cells treated with 5-azacytidine. Cell. 1979 Aug;17(4):771–779. [PubMed] [Google Scholar]
  • Taylor SM, Jones PA. Changes in phenotypic expression in embryonic and adult cells treated with 5-azacytidine. J Cell Physiol. 1982 May;111(2):187–194. [PubMed] [Google Scholar]
  • Urist MR. Bone: formation by autoinduction. Science. 1965 Nov 12;150(3698):893–899. [PubMed] [Google Scholar]
  • Wallace BG. Aggregating factor from Torpedo electric organ induces patches containing acetylcholine receptors, acetylcholinesterase, and butyrylcholinesterase on cultured myotubes. J Cell Biol. 1986 Mar;102(3):783–794. [PMC free article] [PubMed] [Google Scholar]
  • Williams IH, Polakis SE. Differentiation of 3T3-L1 fibroblasts to adipocytes. The effect of indomethacin, prostaglandin E1 and cyclic AMP on the process of differentiation. Biochem Biophys Res Commun. 1977 Jul 11;77(1):175–186. [PubMed] [Google Scholar]
  • Yaffe D. Cellular aspects of muscle differentiation in vitro. Curr Top Dev Biol. 1969;4:37–77. [PubMed] [Google Scholar]
  • Yaffe D. Developmental changes preceding cell fusion during muscle differentiation in vitro. Exp Cell Res. 1971 May;66(1):33–48. [PubMed] [Google Scholar]
  • Yeoh GC, Holtzer H. The effect of cell density, conditioned medium and cytosine arabinoside on myogenesis in primary and secondary cultures. Exp Cell Res. 1977 Jan;104(1):63–78. [PubMed] [Google Scholar]
  • Zalin RJ. The role of hormones and prostanoids in the in vitro proliferation and differentiation of human myoblasts. Exp Cell Res. 1987 Oct;172(2):265–281. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

-