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In vitro differentiation of embryonic stem cells into cardiomyocytes or skeletal muscle cells is specifically modulated by retinoic acid

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Abstract

Pluripotent embryonic stem cells (ES cells) differentiating via embryo-like aggregates (embryoid bodies) into derivatives of the primary germ layers were used as a model system to investigate the time- and concentration dependent effects of retinoic acid (RA) on the in vitro differentiation pattern. When ES cells, cultivated normally under conditions resulting in cardiomyocyte differentiation, were treated during the first 2 days of embryoid body formation with high RA concentrations (10−9 to 10−7 M) a strong inhibition of cardiogenesis was found. ES cells differentiating as embryoid bodies and treated with the same RA concentration between the 5th and 7th day resulted in a slight induction of cardiogenesis. In contrast, incubation of embryoid bodies with 10−8 and 10−7 M RA between the 2nd and 5th day of embryoid body development resulted in a total inhibition of cardiogenesis but in an induction of myogenesis. This was demonstrated by indirect immunofluorescence and, as shown by reverse transcription- polymerase chain reaction (RT-PCR), by the time- and concentration-dependent inhibition of transcription of cardiac-specific α- and β-cardiac myosin heavy chain (MHC) genes, and the induction of transcription of skeletal muscle-specific myogenin. In addition, using the whole-cell patch-clamp technique, these skeletal myocytes were functionally characterized by the expression of tissue-specific Ca2+ channels and nicotinic cholinoceptors. In summary, a specific effect of RA on ES cell differentiation in the embryoid body resulting in a switch from cardiogenesis to myogenesis and an induction of neuronal cells was found.

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References

  • Bader D, Masaki T, Fischman, DA (1982) Immunochemical analysis of myosin heavy chain during avian myogenesis in vivo and in vitro. J Cell Biol 95:763–770

    Google Scholar 

  • Balling R (1991) CRABP and the teratogenic effects of retinoids. Trends Genet 7:35–36

    Google Scholar 

  • Beam KG, Knudson CM (1988) Calcium currents in embryonic and neonatal mammalian skeletal muscle. J Gen Physiol 91:781–798

    Google Scholar 

  • Boncinelli E, Simeone A, Acampora D, Mavilio F (1991) HOX gene activation by retinoic acid. Trends Genet 7:329–334

    Google Scholar 

  • Buckingham M (1992) Making muscle in mammals. Trends Genet 8:144–149

    Google Scholar 

  • Caffrey JM, Brown AM, Schneider MD (1989) Ca2+ and Na+ currents in developing skeletal myoblasts are expressed in a sequential program: reversible suppression by transforming growth factor beta-1, an inhibitor of the myogenic pathway. J Neurosci 9:3443–3453

    Google Scholar 

  • Cho KWY, DeRobertis EM (1990) Differential activation of Xenopus homeobox genes by mesoderm-inducing growth factors and retinoic acid. Genes Dev 4:1910–1916

    Google Scholar 

  • Cognard C, Romey G, Galizzi J-P, Fosset M, Lazdunski M (1986) Different types of Ca2+ channels in mammalian skeletal muscle cells in culture. Proc Natl Acad Sci USA 83:517–521

    Google Scholar 

  • Colquhoun D, Ogden DC, Mathie A (1987) Nicotinic acetylcholine receptors of nerve and muscle: functional aspects. Trends Pharmacol Sci 8:465–472

    Google Scholar 

  • Doetschmann TC, Eistetter HR, Katz M, Schmidt W, Kemler R (1985) The in vitro development of blastocyst-derived embryonic stem cell lines: formation of visceral yolk sac, blood islands and myocardium. J Embryol Exp Morphol 87:27–45

    Google Scholar 

  • Durston AJ, Timmermans JPM, Hage WJ, Hendriks, HFJ, Vries NJ de, Heideveld M, Nieuwkoop PD (1989) Retinoic acid causes an anteroposterior transformation in the developing central nervous system. Nature 340:140–144

    Google Scholar 

  • Edwards MKS, Harris JF, McBurney MW (1983) Induced muscle differentiation in an embryonal carcinoma cell line. Mol Cell Biol 3:2280–2286

    Google Scholar 

  • Eichele G (1989) Retinoids and vertebrate limb pattern formation. Trends Genet 5:246–251

    Google Scholar 

  • Evans MJ, Kaufman MH (1981) Establishment in culture of pluripotent stem cells from mouse embryos. Nature 291:154–156

    Google Scholar 

  • Gonoi T, Hasegawa S (1988) Post-natal disappearance of transient calcium channels in mouse skeletal muscle: Effects of denervation and culture. J Physiol (Lond) 401:617–637

    Google Scholar 

  • Hammil OP, Marty A, Neher E, Sakmann B, Sigworth J (1981) Improved patch-clamp technique for high resolution current recording from cells and cell free membrane patches. Pflügers Arch 391:85–100

    Google Scholar 

  • Hassel JR, Greenberg JH, Johnston MC (1977) Inhibition of cranial neural crest development by vitamin A in the cultured chick embryo. J Morphol 88:49–92

    Google Scholar 

  • Jones-Villeneuve EMV, Rudnicki MA, Harris JF, McBurney MW (1983) Retinoic acid induced neural differentiation of embryonal carcinoma cells. Mol Cell Biol 3:2271–2279

    Google Scholar 

  • Jonk LJC, Jonee MEJ de, Kruyt FA, Mummery CL, Saag P van der, Kruijer W (1992) Aggregation and cell cycle dependent retinoic acid receptor mRNA expression in P19 embryonal carcinoma cells. Mech Dev 36:165–172

    Google Scholar 

  • Kemler R, Brulet P, Schnebelen MT, Gaillard J, Jacob F (1981) Reactivity of monoclonal antibodies against intermediate filament proteins during embryonic development. J Embryol Exp Morphol 64:45–60

    Google Scholar 

  • Kessel M (1992) Respecification of vertebral identities by retinoic acid. Development 115:487–501

    Google Scholar 

  • Kessel M, Gruss P (1991) Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid. Cell 67:89–104

    Google Scholar 

  • Kochhar DM (1973) Limb development in mouse embryos. I. Analysis of teratogenic effects of retinoic acid. Teratology 7:289–298

    Google Scholar 

  • Kruyt FAE, Brink CE van den, Defize LHK, Donath M-J, Kastner P, Kruijer W Chambon P, Saag PT van der (1991) Transcriptional regulation of retinoic acid receptor β in retinoic acid-sensitive and -resistant P19 embryocarcinoma cells. Mech Dev 33:171–178

    Google Scholar 

  • Lammer EJ, Chen DT, Hoar RM, Agnish ND, Benke PJ, Braun JT, Curry CJ, Fernhoff PM, Grix AW Jr, Lott IT, Richard JM, Sun SC (1985) Retinoic acid embryopathy. N Engl J Med 313:837–841

    Google Scholar 

  • Laschinski G, Vogel R, Spielmann H (1991) Cytotoxicity test using blastocyst-derived euploid embryonal stem cells: a new approach to in vitro teratogenesis screening. Reprod Toxicol 5:57–64

    Google Scholar 

  • Lufkin T, Lohnes D, Mark M, Dierich A, Gorry P, Gaub M-P, Le-Meur M, Chambon P (1993) High postnatal lethality and testis degeneration in retinoic acid receptor α mutant mice. Proc Natl Acad Sci USA 90:7225–7229

    Google Scholar 

  • Maltsev V, Rohwedel J, Hescheler J, Wobus AM (1993) Embryonic stem cells differentiate in vitro into cardiomyocytes representing sinusnodal, atrial and ventricular types. Mech Dev 44:41–50

    Google Scholar 

  • Maltsev V, Wobus AM, Rohwedel J, Bader M, Hescheler J (1994) Cardiomyocytes differentiated in vitro from embryonic stem cells developmentally express cardiac-specific genes and ionic currents. Circ Res (in press)

  • Martin G (1981) Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc Natl Acad Sci USA 78:7634–7638

    Google Scholar 

  • Miller-Hance WC, LaCorbiere M, Fuller SJ, Evans SM, Lyons G, Schmidt C, Robbins J, Chien KR (1993) In vitro chamber specification during embryonic stem cell cardiogenesis. J Biol Chem 268:25244–25252

    Google Scholar 

  • Montarras D, Chelly J, Bober E, Arnold H-H, Ott M-O, Gros F, Pinset C (1991) Developmental patterns in the expression of myf5, myoD, myogenin and MRF4 during myogenesis. The New Biologist 3:592–600

    Google Scholar 

  • Morriss GM (1972) Morphogenesis of the malformations induced in rat embryos by maternal hypervitaminosis A. J Anat 113:241–250

    Google Scholar 

  • Morriss GM (1975) Abnormal cell migration as a possible factor in the genesis of vitamin A-induced craniofacial anomalies. In: Neubert D, Merker HJ (eds) New approaches to the evaluation of abnormal embryonic development. Thieme, Stuttgart, pp 678–687

    Google Scholar 

  • Osmond M (1992) The effects of retinoic acid on early heart formation and segmentation in the chick embryo. In: Bellairs R et al. (eds) Formation and differentiation of embryonic mesoderm. Plenum Press, New York, pp 275–300

    Google Scholar 

  • Robbins J, Gulick J, Sanchez A, Howles P, Doetschmann T (1990) Mouse embryonic stem cells express the cardiac myosin heavy chain genes during development in vitro. J Biol Chem 265:11905–11909

    Google Scholar 

  • Robertson EJ (1987) Embryo-derived stem cell lines. In: Robertson EJ (ed) Teratocarcinomas and embryonic stem cells. A practical approach. IRL Press, Oxford Washington, pp 71–112

    Google Scholar 

  • Rohwedel J, Maltsev V, Bober E, Arnold H-H, Hescheler J, Wobus AM (1994) Myogenesis in vitro: Developmental expression of skeletal muscle determination genes and ionic currents in embryonic stem cell (ESC)-derived myocytes. Dev Biol 163 (in press)

  • Ruberte E, Dolle P, Krust A, Zelent A, Morriss-Kay G, Chambon P (1990) Specific spatial and temporal distribution of retinoic acid receptor gamma transcripts during mouse embryogenesis. Development 108:213–222

    Google Scholar 

  • Ruberte E, Dolle P, Chambon P, Murriss-Kay G (1991) Retinoic acid receptors and cellular retinoid binding proteins. II. Their differential pattern of transcription during early morphogenesis in mouse embryos. Development 111:45–60

    Google Scholar 

  • Rudniclci MA, McBurney MW (1987) Cell culture methods and induction of differentiation of embryonal carcinoma cell lines. In: Robertson EJ (ed) Teratocarcinomas and embryonic stem cells. IRL Press, Oxford Washington, pp 19–49

    Google Scholar 

  • Rudniclci MA, Jackowski G, Saggin L, McBurney MW (1990) Actin and myosin expression during development of cardiac muscle from cultured embryonal carcinoma cells. Dev Biol 138:348–358

    Google Scholar 

  • Ruiz i Altaba A, Jessel T (1991) Rednoic acid modifies mesodermal patterning in early Xenopus embryos. Genes Dev 5:175–187

    Google Scholar 

  • Sassoon D, Lyons G, Wright WE, Lin V, Lassar A, Weintraub H, Buckingham M (1989) Expression of two myogenic regulatory factors myogenin and MyoDl during mouse embryogenesis. Nature 341:303–307

    Google Scholar 

  • Sharpe CR (1991) Retinoic acid can mimic endogenous signals involved in transformation of the Xenopus nervous system. Neuron 7:239–247

    Google Scholar 

  • Sheardown SA (1992) A simple method for affinity purification and PCR amplification of poly(A)+ mRNA. Trends Genet 8:121

    Google Scholar 

  • Shimahara T, Bournaud R (1991) Barium currents in developing skeletal muscle cells of normal and mutant mice foetuses with “muscular dysgenesis”. Cell Calcium 12:727–733

    Google Scholar 

  • Simeone A, Acampora D, Arcioni L, Andrews PW, Boncinelli E, Mavilio F (1990) Sequential activation of HOX2 homeobox genes by retinoic acid in human embryonal carcinoma cells. Nature (Lond) 346:763–766

    Google Scholar 

  • Simeone A, Acampora D, Nigro V, Faiella A, D'Esposito M, Stornaiuolo A, Mavilio F, Boncinelli E (1991) Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells. Mech Dev 33:215–228

    Google Scholar 

  • Sive HL, Cheng PF (1991) Retinoic acid perturbs the expression of Xhox.lab genes and alters mesodermal determination in Xenopus laevis. Genes Dev 5:1321–1332

    Google Scholar 

  • Sive HL, Draper BW, Harland RW, Weintraub H (1990) Identification of a retinoic acid-sensitive period during primary axis formation in Xenopus laevis. Genes Dev 4:932–942

    Google Scholar 

  • Solter D, Knowles BB (1978) Monoclonal antibody defining a stage specific mouse embryonic antigen (SSEA-1). Proc Natl Acad Sci 75:5565–5568

    Google Scholar 

  • Steinbach JH (1989) Structural and functional diversity in vertebrate skeletal muscle nicotinic acetylcholine receptors. Annu Rev Physiol 51:353–365

    Google Scholar 

  • Tabin CJ (1991) Retinoids, homeoboxes, and growth factors: Toward molecular models for limb development. Cell 66:199–217

    Google Scholar 

  • Van den Eijnden-van Raaij AJM, Achterberg TAE van, Kruijssen CMM van der, Piersma AH, Huylebroeck D, Laat SW de, Mummery CL (1991) Differentiation of aggregated murine P19 embryonal carcinoma cells is induced by a novel visceral endoderm-specific FGF-like factor and inhibited by activin A. Mech Dev 33:157–166

    Google Scholar 

  • Walter G, Intek A, Wobus AM, Schöneich J (1984) Serological characterization of a pluripotent mouse embryonal stem cell line, two transformed derivatives, and an endoderm-like cell line. Cell Differentiation 15:147–151

    Google Scholar 

  • Wilkinson DG, Bhatt S, Cook M, Boncinelli E, Krumlauf R (1989) Segmental expression of Hox-2 homeobox-containing genes in the developing mouse hindbrain. Nature 341:405–409

    Google Scholar 

  • Wobus AM, Holzhausen H, Jäkel P, Schöneich J (1984) Characterization of a pluripotent stem cell line derived from a mouse embryo. Exp Cell Res 152:212–219

    Google Scholar 

  • Wobus AM, Wallukat G, Hescheler J (1991) Pluripotent mouse embryonic stem cells are able to differentiate into cardiomyocytes expressing chronotropic responses to adrenergic and cholinergic agents and Ca2+ channel blockers. Differentiation 48:173–182

    Google Scholar 

  • Wobus AM, Kleppisch T, Maltsev V, Hescheler J (1994) Functional expression of a drenoceptors and Ca2+ channels in cardiomyocyte-like cells differentiated from embryonic carcinoma cells (ECC) in vitro. In vitro Cell Dev Biol (in press)

  • Wright CVE, Cho KWY, Hardwicke J, Collins RH, DeRobertis EM (1989) Interference with function of a homeobox gene in Xenopus embryos produces malformations of the anterior spinal cord. Cell 59:81–93

    Google Scholar 

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Wobus, A.M., Rohwedel, J., Maltsev, V. et al. In vitro differentiation of embryonic stem cells into cardiomyocytes or skeletal muscle cells is specifically modulated by retinoic acid. Roux's Arch Dev Biol 204, 36–45 (1994). https://doi.org/10.1007/BF00189066

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