Literature DB >> 11437454

Novel cell lines promote the discovery of genes involved in early heart development.

E W Brunskill1, D P Witte, K E Yutzey, S S Potter.   

Abstract

Clonal cell lines representing early cardiomyocytes would provide valuable reagents for the dissection of the genetic program of early cardiogenesis. Here we describe the establishment and characterization of cell lines from the hearts of transgenic mice and embryos with SV40 large T antigen expressed in the heart-forming region. Ultrastructure analysis by transmission electron microscopy showed the primitive, precontractile nature of the resulting cells, with the absence of myofilaments, Z lines, and intercalated disks. Immunohistochemistry, RT-PCR, Northern blots, and oligonucleotide microarrays were used to determine the expression levels of thousands of genes in the 1H and ECL-2 cell lines. The resulting gene-expression profiles showed the transcription of early cardiomyocyte genes such as Nkx2.5, GATA4, Tbx5, dHAND, cardiac troponin C, and SM22-alpha. Furthermore, many genes not previously implicated in early cardiac development were expressed. Two of these genes, Hic-5, a possible negative regulator of muscle differentiation, and the transcription enhancing factor TEF-5 were selected and shown by in situ hybridizations to be expressed in the early developing heart. The results show that the 1H and ECL-2 cell lines can be used to discover novel genes expressed in the early cardiomyocyte. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11437454     DOI: 10.1006/dbio.2001.0313

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  11 in total

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2.  Transforming growth factor-β1-induced transcript 1 protein, a novel marker for smooth muscle contractile phenotype, is regulated by serum response factor/myocardin protein.

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3.  Expression of focal adhesion proteins in the developing rat kidney.

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4.  Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome.

Authors:  Erica Hasten; Donna M McDonald-McGinn; Terrence B Crowley; Elaine Zackai; Beverly S Emanuel; Bernice E Morrow; Silvia E Racedo
Journal:  Hum Mol Genet       Date:  2018-06-01       Impact factor: 6.150

5.  The H9C2 cell line and primary neonatal cardiomyocyte cells show similar hypertrophic responses in vitro.

Authors:  Sarah J Watkins; Gillian M Borthwick; Helen M Arthur
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6.  Down-regulation of SM22/transgelin gene expression during H9c2 cells differentiation.

Authors:  Elisa Bregant; Giovanni Renzone; Renata Lonigro; Nadia Passon; Carla Di Loreto; Maura Pandolfi; Andrea Scaloni; Gianluca Tell; Giuseppe Damante
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7.  Hic-5 is required for fetal gene expression and cytoskeletal organization of neonatal cardiac myocytes.

Authors:  Erin E Yund; Joseph A Hill; Rebecca S Keller
Journal:  J Mol Cell Cardiol       Date:  2009-06-18       Impact factor: 5.000

8.  GATA4 transgenic mice as an in vivo model of congenital heart disease.

Authors:  Hua Han; Yu Chen; Gang Liu; Zengqiang Han; Zhou Zhao; Yin Tang
Journal:  Int J Mol Med       Date:  2015-04-09       Impact factor: 4.101

9.  Hic-5 regulates epithelial to mesenchymal transition in ovarian cancer cells in a TGFβ1-independent manner.

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Journal:  Oncotarget       Date:  2017-07-31

10.  Tissue specific promoters improve specificity of AAV9 mediated transgene expression following intra-vascular gene delivery in neonatal mice.

Authors:  Christina A Pacak; Yoshihisa Sakai; Bijoy D Thattaliyath; Cathryn S Mah; Barry J Byrne
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