Literature DB >> 3902781

Factors controlling embryonic heart cell proliferation in serum-free synthetic media.

A C Nag, M Ingland, M Cheng.   

Abstract

Embryonic chick cardiac cell cultures, plated on collagen-coated dishes, containing serum-free synthetic media proliferate actively. The basic medium contained Ham's F12 nutrient mixture, fetuin, ascorbic acid, and bovine serum albumin. This medium was supplemented with various combinations of factors: endothelial cell growth supplement (ECGS), epidermal growth factor (EGF), insulin (I), transferrin (T), selenium (S), hydrocortisone, and thyroxine or supplemented alone. Basic medium supplemented with ECGS alone contributes to the highest final cell density among all other factors used in various combinations or alone. The final cell density of the control culture with 2% fetal bovine serum was higher than those of all experimental cultures and an additional control culture grown in the basic medium. Combinations of factors without ECGS do not promote significant cell proliferation. Thyroxine is required to induce optimal differentiation and contractility of cardiac myocytes in vitro. Fibronectin and laminin did not show any more influence than collagen did on the growth and maintenance of cardiac myocytes in serum-free media. The proportion of cardiac muscle cells in ECGS-containing media was higher than those in other experimental media and control media with the exception of ECGS and ITS-containing medium that showed lower proportion of cardiac myocytes than that of serum-containing medium on Days 3 and 5. The profiles of incorporation of [3H]thymidine into DNA of heart cells in experimental and control cultures showed a peak in incorporation values within the first week of culture and subsequently declined. Autoradiography studies revealed that cardiac myocytes in culture supplemented with ECGS alone attained a peak in labeling index on Day 1 with approximately 62% labeled cells. Subsequently, the labeling indices declined. Cardiac myocytes grown in media without ECGS showed significantly lower labeling indices than those in ECGS-containing media. This study has demonstrated the influence of ECGS, EGF and ITS in promoting the growth of cardiac myocytes and also in contributing to the maintenance of contractile cardiac myocytes in serum-free, long-term culture. The influence of ECGS on heart cell proliferation is considered to be superior to that of EGF and ITS.

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Year:  1985        PMID: 3902781     DOI: 10.1007/bf02620885

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  16 in total

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Authors:  B CEDERGREN; I HARARY
Journal:  J Ultrastruct Res       Date:  1964-12

2.  Rat myocardial cells in vitro: mitosis and differentiated properties.

Authors:  F H Kasten
Journal:  In Vitro       Date:  1972 Nov-Dec

3.  Growth and DNA synthesis in embryonic chick heart cells, in vivo and in vitro.

Authors:  I S Polinger
Journal:  Exp Cell Res       Date:  1973-02       Impact factor: 3.905

4.  Diffusion-mediated control of myoblast fusion.

Authors:  I R Konigsberg
Journal:  Dev Biol       Date:  1971-09       Impact factor: 3.582

5.  DNA synthesis, mitosis, and differentiation in cardiac myogenesis.

Authors:  S Chacko
Journal:  Dev Biol       Date:  1973-11       Impact factor: 3.582

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Authors:  W C Claycomb
Journal:  Exp Cell Res       Date:  1981-01       Impact factor: 3.905

7.  A serum-free, chemically-defined medium for function and growth of primary neonatal rat heart cell cultures.

Authors:  S N Mohamed; R Holmes; C R Hartzell
Journal:  In Vitro       Date:  1983-06

8.  Analysis of population cytokinetics of chick myocardial cells in tissue culture.

Authors:  W A Clark; D A Fischman
Journal:  Dev Biol       Date:  1983-05       Impact factor: 3.582

9.  Competence of embryonic mammalian heart cells in culture: DNA synthesis, mitosis and differentiation.

Authors:  A C Nag; T F Crandell; M Cheng
Journal:  Cytobios       Date:  1981

10.  An endothelial cell growth factor from bovine hypothalamus: identification and partial characterization.

Authors:  T Maciag; J Cerundolo; S Ilsley; P R Kelley; R Forand
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

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  4 in total

1.  Serum-free, chemically defined medium to evaluate the direct effects of growth factors and inhibitors on proliferation and function of neonatal rat cardiac muscle cells in culture.

Authors:  T Suzuki; M Ohta; H Hoshi
Journal:  In Vitro Cell Dev Biol       Date:  1989-07

2.  Remodelling of adult cardiac muscle cells in culture: dynamic process of disorganization and reorganization of myofibrils.

Authors:  A C Nag; M L Lee; F H Sarkar
Journal:  J Muscle Res Cell Motil       Date:  1996-06       Impact factor: 2.698

3.  Immunocytochemical studies of cardiac myocytes and other non-neuronal cells of the fetal human heart in culture.

Authors:  C J Hassall; R Penketh; C Rodeck; G Burnstock
Journal:  Anat Embryol (Berl)       Date:  1990

4.  Stimulation and inhibition of cardiac myocyte proliferation in vitro.

Authors:  E Kardami
Journal:  Mol Cell Biochem       Date:  1990-02-09       Impact factor: 3.396

  4 in total

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