Literature DB >> 8838663

Conditional differentiation of heart- and smooth muscle-derived cells transformed by a temperature-sensitive mutant of SV40 T antigen.

L Jahn1, J Sadoshima, A Greene, C Parker, K G Morgan, S Izumo.   

Abstract

To create muscle cell lines that conditionally differentiate in vitro we introduced a temperature-sensitive SV40 T antigen by retroviral infection into rat aortic smooth muscle cells (SMCs) and neonatal heart-derived cells. After G418 selection cell lines isolated were characterized at permissive (33 degrees C) and non-permissive (39 degrees C) temperatures. [3H]Thymidine uptake showed tht progression through the cell cycle is greatly reduced at 39 degrees C. Cytoskeletal proteins, such as actins and vimentin did not change significantly after temperature shift, while the number of desmin-positive SMCs significantly increased when cells were switched to 39 degrees C. Heart-derived muscle cells showed sarcomeric myosin heavy chain reactivity only when grown at 39 degrees C. After thrombin stimulation intracellular calcium in both cell types increased severalfold in 39 degrees C-cells but not in 33 degrees C-cells. Whole cell patch-clamp recordings of SMCs and heart-derived cells revealed a strong increase in nicardipine-sensitive Ca2+ current when cells were switched to 39 degrees C. Nicardipine-insensitive Ca2+ current also increased in both cell types at the non-permissive temperature. Na+ current in SMCs was large at 33 degrees C and small or not detectable at 39 degrees C and absent in heart-derived cells. Using a cDNA probe specific for the alpha 1 subunit of the dihydropyridine-sensitive Ca2+ channel we demonstrate a temperature-sensitive expression of the dihydropyridine receptor mRNA in smooth muscle-derived cells but not in heart-derived H10 cells. Our results suggest that upon downregulation of SV40 T antigen these cells become quiescent and exhibit a more differentiated phenotype. These cell lines may provide a useful tool to investigate ion channel- and receptor signal transduction, as well as cell cycle control in smooth and possibly cardiac muscle cell differentiation.

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Year:  1996        PMID: 8838663     DOI: 10.1242/jcs.109.2.397

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  12 in total

1.  The MRE11-NBS1-RAD50 pathway is perturbed in SV40 large T antigen-immortalized AT-1, AT-2 and HL-1 cardiomyocytes.

Authors:  N A Lanson; D B Egeland; B A Royals; W C Claycomb
Journal:  Nucleic Acids Res       Date:  2000-08-01       Impact factor: 16.971

2.  Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria.

Authors:  Willem M H Hoogaars; Angela Engel; Janynke F Brons; Arie O Verkerk; Frederik J de Lange; L Y Elaine Wong; Martijn L Bakker; Danielle E Clout; Vincent Wakker; Phil Barnett; Jan Hindrik Ravesloot; Antoon F M Moorman; E Etienne Verheijck; Vincent M Christoffels
Journal:  Genes Dev       Date:  2007-05-01       Impact factor: 11.361

3.  Differential interaction of temperature-sensitive simian virus 40 T antigens with tumor suppressors pRb and p53.

Authors:  S Ray; M E Anderson; P Tegtmeyer
Journal:  J Virol       Date:  1996-10       Impact factor: 5.103

4.  HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte.

Authors:  W C Claycomb; N A Lanson; B S Stallworth; D B Egeland; J B Delcarpio; A Bahinski; N J Izzo
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

5.  Human myocardial cell lines generated with SV40 temperature-sensitive mutant tsA58.

Authors:  Bruce I Goldman; Kunjlata M Amin; Hajime Kubo; Arun Singhal; John Wurzel
Journal:  In Vitro Cell Dev Biol Anim       Date:  2006 Nov-Dec       Impact factor: 2.416

6.  Overlapping roles of pocket proteins in the myocardium are unmasked by germ line deletion of p130 plus heart-specific deletion of Rb.

Authors:  W R MacLellan; A Garcia; H Oh; P Frenkel; M C Jordan; K P Roos; M D Schneider
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

7.  Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner.

Authors:  Ahmad S Amin; John R Giudicessi; Anke J Tijsen; Anne M Spanjaart; Yolan J Reckman; Christine A Klemens; Michael W Tanck; Jamie D Kapplinger; Nynke Hofman; Moritz F Sinner; Martina Müller; Wino J Wijnen; Hanno L Tan; Connie R Bezzina; Esther E Creemers; Arthur A M Wilde; Michael J Ackerman; Yigal M Pinto
Journal:  Eur Heart J       Date:  2011-12-23       Impact factor: 29.983

8.  Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation.

Authors:  Christiaan C Veerman; Isabella Mengarelli; Elisabeth M Lodder; Georgios Kosmidis; Milena Bellin; Miao Zhang; Sven Dittmann; Kaomei Guan; Arthur A M Wilde; Eric Schulze-Bahr; Boris Greber; Connie R Bezzina; Arie O Verkerk
Journal:  J Am Heart Assoc       Date:  2017-07-24       Impact factor: 5.501

9.  Generation and primary characterization of iAM-1, a versatile new line of conditionally immortalized atrial myocytes with preserved cardiomyogenic differentiation capacity.

Authors:  Jia Liu; Linda Volkers; Wanchana Jangsangthong; Cindy I Bart; Marc C Engels; Guangqian Zhou; Martin J Schalij; Dirk L Ypey; Daniël A Pijnappels; Antoine A F de Vries
Journal:  Cardiovasc Res       Date:  2018-12-01       Impact factor: 10.787

10.  The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.

Authors:  Klaartje van Engelen; Mathilda T M Mommersteeg; Marieke J H Baars; Jan Lam; Aho Ilgun; A S Paul van Trotsenburg; Anne M J B Smets; Vincent M Christoffels; Barbara J M Mulder; Alex V Postma
Journal:  PLoS One       Date:  2012-12-28       Impact factor: 3.240

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