Literature DB >> 15064945

Heart-type fatty acid binding proteins are upregulated during terminal differentiation of mouse cardiomyocytes, as revealed by proteomic analysis.

M K Tang1, P M Kindler, D Q Cai, P H Chow, M Li, K K H Lee.   

Abstract

At birth, the cardiomyocytes in the mouse neonatal heart still retain their ability to proliferate. However, this lasts only a few days and then the cardiomyocytes irreversibly lose their potential to divide. It is still not fully understood what factors are involved in the cessation of cardiomyocyte proliferation. Using proliferating cell nuclear antigen (PCNA) antibodies, we established that cardiomyocytes could divide extensively in 2-day-old mouse neonatal hearts and to a lesser extent in 6-day-old hearts. By 13 days, the cardiomyocytes have mostly stopped dividing. Comparative two-dimensional gel electrophoresis (2-DE) was performed on total proteins extracted from the 2-day- and 13-day-old hearts, in order to identify peptides that might be involved in the inhibition of cardiomyocyte proliferation. Using matrix-assisted laser desorption ionization mass spectroscopy (MALDI-TOF), we identified two protein spots that have the same molecular weight (approximately 14 kDa) but different pIs (5.9 and 6.1). Mass spectra analysis determined the proteins to be isoforms of the heart-type fatty acid binding protein (H-FABP). The pI 6.1 H-FABP is also known as mammary-derived growth inhibitor (MDGI; Specht et al. 1996). MGDI is a breast tumour growth suppressor gene capable of inhibiting tumour cell proliferation (Huynh et al. 1995). Both H-FABP isoforms were expressed in 2-day-old hearts but became strongly upregulated in 13-day-old hearts. We examined whether H-FABPs and PCNA were coexpressed in 2-, 6- and 13-day-old heart histological sections, using MDGI antibodies. The antibody could detect both forms of H-FABPs. It was established that there was a correlation between an increase in H-FABP expression and a decrease in PCNA expression. Hence, we tentatively propose that H-FABP isoforms are involved in regulating cardiomyocyte growth and differentiation in mouse neonatal hearts.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15064945     DOI: 10.1007/s00441-004-0881-y

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  12 in total

Review 1.  The multigene family of fatty acid-binding proteins (FABPs): function, structure and polymorphism.

Authors:  Agata Chmurzyńska
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

2.  Gene expression in rats with Barrett's esophagus and esophageal adenocarcinoma induced by gastroduodenoesophageal reflux.

Authors:  Peng Cheng; Jun Gong; Tao Wang; Jie Chen; Gui-Sheng Liu; Ru Zhang
Journal:  World J Gastroenterol       Date:  2005-09-07       Impact factor: 5.742

3.  Silencing of FABP3 promotes apoptosis and induces mitochondrion impairment in embryonic carcinoma cells.

Authors:  Ya-Hui Shen; Gui-Xian Song; Yao-Qiu Liu; Wei Sun; Li-Juan Zhou; Hai-Lang Liu; Rong Yang; Yan-Hui Sheng; Ling-Mei Qian; Xiang-Qing Kong
Journal:  J Bioenerg Biomembr       Date:  2012-04-20       Impact factor: 2.945

Review 4.  Tissue-specific functions in the fatty acid-binding protein family.

Authors:  Judith Storch; Alfred E Thumser
Journal:  J Biol Chem       Date:  2010-08-17       Impact factor: 5.157

5.  Overexpression of FABP3 inhibits human bone marrow derived mesenchymal stem cell proliferation but enhances their survival in hypoxia.

Authors:  Suna Wang; Yifu Zhou; Oleg Andreyev; Robert F Hoyt; Avneesh Singh; Timothy Hunt; Keith A Horvath
Journal:  Exp Cell Res       Date:  2014-02-27       Impact factor: 3.905

6.  microRNA-1 inhibits cardiomyocyte proliferation in mouse neonatal hearts by repressing CCND1 expression.

Authors:  Jingyi Gan; Florence Mei Kuen Tang; Xianwei Su; Gang Lu; Jing Xu; Henry Siu Sum Lee; Kenneth Ka Ho Lee
Journal:  Ann Transl Med       Date:  2019-09

7.  Knockdown of FABP3 impairs cardiac development in Zebrafish through the retinoic acid signaling pathway.

Authors:  Xuejie Wang; Lijuan Zhou; Jin Jin; Yang Yang; Guixian Song; Yahui Shen; Hailang Liu; Ming Liu; Chunmei Shi; Lingmei Qian
Journal:  Int J Mol Sci       Date:  2013-07-03       Impact factor: 5.923

8.  Fabp3 inhibits proliferation and promotes apoptosis of embryonic myocardial cells.

Authors:  C Zhu; D L Hu; Y Q Liu; Q J Zhang; F K Chen; X Q Kong; K J Cao; J S Zhang; L M Qian
Journal:  Cell Biochem Biophys       Date:  2011-07       Impact factor: 2.194

9.  Integrative Analysis of the Developing Postnatal Mouse Heart Transcriptome.

Authors:  Jingyi Gan; Hans-Joachim Sonntag; Mei Kuen Tang; Dongqing Cai; Kenneth Ka Ho Lee
Journal:  PLoS One       Date:  2015-07-22       Impact factor: 3.240

10.  Brain fatty acid binding protein (Fabp7) is diurnally regulated in astrocytes and hippocampal granule cell precursors in adult rodent brain.

Authors:  Jason R Gerstner; Quentin Z Bremer; William M Vander Heyden; Timothy M Lavaute; Jerry C Yin; Charles F Landry
Journal:  PLoS One       Date:  2008-02-20       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.