Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 May 1;102(2):194-204.
doi: 10.1093/cvr/cvu021. Epub 2014 Jan 29.

Signalling between microvascular endothelium and cardiomyocytes through neuregulin

Affiliations
Review

Signalling between microvascular endothelium and cardiomyocytes through neuregulin

Emily M Parodi et al. Cardiovasc Res. .

Abstract

Heterocellular communication in the heart is an important mechanism for matching circulatory demands with cardiac structure and function, and neuregulins (Nrgs) play an important role in transducing this signal between the hearts' vasculature and musculature. Here, we review the current knowledge regarding Nrgs, explaining their roles in transducing signals between the heart's microvasculature and cardiomyocytes. We highlight intriguing areas being investigated for developing new, Nrg-mediated strategies to heal the heart in acquired and congenital heart diseases, and note avenues for future research.

Keywords: ErbB; Heart; Heterocellular communication; Neuregulin.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Nrg isoform structures: Nrg structures. (A) NRG-1 and NRG-2 genetic loci. (B) NRG-1 and NRG-2 protein isoform compositions. Arrows indicate putative proteolytic sites.
Figure 2
Figure 2
Nrg-1 heterocellular signalling: (A) Nrg heterocellular signalling between a coronary microvascular endothelial cell (top) and a cardiomyocyte (bottom). Scissor indicates proteolytic cleavage by metalloproteinases. The green box in (iv) indicates receptor phosphorylation and activation. (B) Nrg heterocellular signalling drives post-natal lobuloalveolar mammary gland changes upon pregnancy.
Figure 3
Figure 3
Nrg-1 ligand and receptor localizations: (top panel) tissues expressing Nrg1 during pre and post-natal life. (Middle panel) ErbB2 and ErbB4 expression profiles. (Bottom panel) ErbB3 and ErbB4 expression profiles. Disease expression indicates tissues overexpressing Nrg (top) or its receptors (middle, bottom) concomitant with indicated diseases.

References

    1. Peles E, Yarden Y. Neu and its ligands: from an oncogene to neural factors. BioEssays News Rev Mol Cell Dev Biol. 1993;15:815–824. - PubMed
    1. Carraway KL, III, Weber JL, Unger MJ, Ledesma J, Yu N, Gassmann M, et al. Neuregulin-2, a new ligand of ErbB3/ErbB4-receptor tyrosine kinases. Nature. 1997;387:512–516. - PubMed
    1. Zhang D, Sliwkowski MX, Mark M, Frantz G, Akita R, Sun Y, et al. Neuregulin-3 (NRG3): a novel neural tissue-enriched protein that binds and activates ErbB4. Proc Natl Acad Sci USA. 1997;94:9562–9567. - PMC - PubMed
    1. Harari D, Tzahar E, Romano J, Shelly M, Pierce JH, Andrews GC, et al. Neuregulin-4: a novel growth factor that acts through the ErbB-4 receptor tyrosine kinase. Oncogene. 1999;18:2681–2689. - PubMed
    1. Hidalgo A, Kinrade EF, Georgiou M. The Drosophila neuregulin vein maintains glial survival during axon guidance in the CNS. Dev Cell. 2001;1:679–690. - PubMed

Publication types