Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein

被引:130
|
作者
Kasahara, H
Bartunkova, S
Schinke, M
Tanaka, M
Izumo, S
机构
[1] Beth Israel Deaconess Med Ctr, Div Cardiovasc, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
homeobox gene; Csx; Nkx2.5; cardiac development; immunohistochemistry; NK-2;
D O I
10.1161/01.RES.82.9.936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Csx/Nkx2.5 is an evolutionary conserved homeobox gene related to the Drosophila tinman gene, which is essential for the dorsal mesoderm formation. Expression of Csx/Nkx2.5 mRNA is the earliest marker for heart precursor cells in all vertebrates so far examined. Previous studies have demonstrated that Csx/Nkx2.5 mRNA is highly expressed in the heart and at lower levels in the spleen, tongue, stomach, and thyroid in the murine embryo, Since some developmental genes are regulated by posttranscriptional mechanisms, we analyzed the developmental pattern of Csx protein expression at the single-cell level using Csx-specific antibodies. Immunohistochemical analysis of murine embryos at 7.8 days post coitum revealed that Csx protein is strongly expressed in the nucleus of endodermal and mesodermal cells in the cardiogenic plate. Subsequently, in the heart, Car protein was detected only in the nucleus of myocytes of the atrium and the ventricle through the adult stage. During the fetal period, Csx protein expression in the nucleus was also noted in the spleen, stomach, liver, tongue, and anterior larynx. Unexpectedly, confocal microscopy revealed that Csx immunoreactivity was detected only in the cytoplasm of a subset of cranial skeletal muscles. Csx protein was not detected in the thyroid glands. The expression of Csx protein in all organs was markedly downregulated after birth except in the heart. These results raise the possibility that Csx/Nkx2.5 may play a role in the early developmental process of multiple tissues in addition to its role in early heart development.
引用
收藏
页码:936 / 946
页数:11
相关论文
共 50 条
  • [31] Carboxyl terminus of NKX2.5 impairs its interaction with p300
    Li, Tao
    Li, Yan-Ming
    Jia, Zhu-Qing
    Chen, Ping
    Ma, Kang-Tao
    Zhou, Chun-Yan
    JOURNAL OF MOLECULAR BIOLOGY, 2007, 370 (05) : 976 - 992
  • [32] NKX2.5 mutations in patients with non-syndromic congenital heart disease
    Gioli-Pereira, Luciana
    Pereira, Alexandre Costa
    Mesquita, Sonia M.
    Xavier-Neto, Jose
    Lopes, Antonio Augusto
    Krieger, Jose Eduardo
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 138 (03) : 261 - 265
  • [33] Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism
    Khatami, Mehri
    Heidari, Mohammad Mehdi
    Tabesh, Fatemeh
    Ordooei, Mahtab
    Salehifar, Zohreh
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2017, 30 (08) : 857 - 862
  • [34] NKX2.5 is expressed in papillary thyroid carcinomas and regulates differentiation in thyroid cells
    Cardoso Penha, Ricardo Cortez
    Buexm, Luisa Aguirre
    Rodrigues, Fabiana Resende
    de Castro, Taciana Padilha
    Santos, Maria Carolina S.
    Fortunato, Rodrigo Soares
    Carvalho, Denise P.
    Cardoso-Weide, Luciene C.
    Ferreira, Andrea C. F.
    BMC CANCER, 2018, 18
  • [35] Nkx2.5 is essential to establish normal heart rate variability in the zebrafish embryo
    Harrington, Jamie K.
    Sorabella, Robert
    Tercek, Abigail
    Isler, Joseph R.
    Targoff, Kimara L.
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2017, 313 (03) : R265 - R271
  • [36] Developmentally modulated cardiac conduction failure in transgenic mice with fetal or postnatal overexpression of DNA nonbinding mutant Nkx2.5
    Wakimoto, H
    Kasahara, H
    Maguire, CT
    Izumo, S
    Berul, CI
    JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2002, 13 (07) : 682 - 688
  • [37] Novel NKX2.5 variant associated with congenital heart disease and increased risk of malignant arrhythmia and sudden cardiac death
    Helm, Benjamin M.
    Baud, Rebecca
    Shopp, Laura
    Kean, Adam C.
    Ayers, Mark D.
    CARDIOLOGY IN THE YOUNG, 2024, 34 (03) : 654 - 658
  • [38] Differential regulation of the cardiac sodium calcium exchanger promoter in adult and neonatal cardiomyocytes by Nkx2.5 and serum response factor
    Müller, JG
    Thompson, JT
    Edmonson, AM
    Rackley, MS
    Kasahara, H
    Izumo, S
    McQuinn, TC
    Menick, DR
    O'Brien, TX
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (07) : 807 - 821
  • [39] Hexabromocyclododecane exposure induces cardiac hypertrophy and arrhythmia by inhibiting miR-1 expression via up-regulation of the homeobox gene Nkx2.5
    Wu, Meifang
    Wu, Di
    Wang, Chonggang
    Guo, Zhizhun
    Li, Bowen
    Zuo, Zhenghong
    JOURNAL OF HAZARDOUS MATERIALS, 2016, 302 : 304 - 313
  • [40] NKX2.5 is expressed in papillary thyroid carcinomas and regulates differentiation in thyroid cells
    Ricardo Cortez Cardoso Penha
    Luisa Aguirre Buexm
    Fabiana Resende Rodrigues
    Taciana Padilha de Castro
    Maria Carolina S. Santos
    Rodrigo Soares Fortunato
    Denise P. Carvalho
    Luciene C. Cardoso-Weide
    Andrea C. F. Ferreira
    BMC Cancer, 18