» Articles » PMID: 25649302

Cardiomyocyte Protein Trafficking: Relevance to Heart Disease and Opportunities for Therapeutic Intervention

Overview
Date 2015 Feb 5
PMID 25649302
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Cardiomyocytes, the individual contractile units of heart muscle, are long-lived and robust. Given the longevity of these cells, it can be easy to overlook their dynamic intracellular environment that contain rapid protein movements and frequent protein turnover. Critical gene transcription and protein translation occur continuously, as well as trafficking and localization of proteins to specific functional zones of cell membrane. As heart failure becomes an increasingly important clinical entity, growing numbers of investigative teams are examining the cell biology of healthy and diseased cardiomyocytes. In this review, we introduce the major architectural structures and types of protein movements within cardiac cells, and then review recent studies that explore the regulation of such movements. We conclude by introducing current translational directions of the basic studies with a focus on novel areas of therapeutic development.

Citing Articles

Biochemical Structure and Function of TRAPP Complexes in the Cardiac System.

Papaioannou P, Wallace M, Malhotra N, Mohler P, El Refaey M JACC Basic Transl Sci. 2024; 8(12):1599-1612.

PMID: 38205348 PMC: 10774597. DOI: 10.1016/j.jacbts.2023.03.011.


Stx4 is required to regulate cardiomyocyte Ca handling during vertebrate cardiac development.

Perl E, Ravisankar P, Beerens M, Mulahasanovic L, Smallwood K, Sasso M HGG Adv. 2022; 3(3):100115.

PMID: 35599850 PMC: 9114686. DOI: 10.1016/j.xhgg.2022.100115.


Controlling the Traffic to Keep the Beat: Targeting of Myocardial Sodium Channels.

Nerbonne J Circ Res. 2021; 129(3):366-368.

PMID: 34292782 PMC: 8318379. DOI: 10.1161/CIRCRESAHA.121.319653.


Membrane Physiology and Biophysics-What Remains to Be Done?.

Fahlke C Front Physiol. 2020; 11:892.

PMID: 32848847 PMC: 7399167. DOI: 10.3389/fphys.2020.00892.


β-adrenergic-mediated dynamic augmentation of sarcolemmal Ca 1.2 clustering and co-operativity in ventricular myocytes.

Ito D, Hannigan K, Ghosh D, Xu B, Del Villar S, Xiang Y J Physiol. 2019; 597(8):2139-2162.

PMID: 30714156 PMC: 6462464. DOI: 10.1113/JP277283.


References
1.
Ul-Hussain M, Olk S, Schoenebeck B, Wasielewski B, Meier C, Prochnow N . Internal ribosomal entry site (IRES) activity generates endogenous carboxyl-terminal domains of Cx43 and is responsive to hypoxic conditions. J Biol Chem. 2014; 289(30):20979-90. PMC: 4110304. DOI: 10.1074/jbc.M113.540187. View

2.
Itoh T, Erdmann K, Roux A, Habermann B, Werner H, De Camilli P . Dynamin and the actin cytoskeleton cooperatively regulate plasma membrane invagination by BAR and F-BAR proteins. Dev Cell. 2005; 9(6):791-804. DOI: 10.1016/j.devcel.2005.11.005. View

3.
Luini A, Mironov A, Polishchuk E, Polishchuk R . Morphogenesis of post-Golgi transport carriers. Histochem Cell Biol. 2008; 129(2):153-61. PMC: 2228382. DOI: 10.1007/s00418-007-0365-8. View

4.
Hong T, Smyth J, Gao D, Chu K, Vogan J, Fong T . BIN1 localizes the L-type calcium channel to cardiac T-tubules. PLoS Biol. 2010; 8(2):e1000312. PMC: 2821894. DOI: 10.1371/journal.pbio.1000312. View

5.
Lyon A, Nikolaev V, Miragoli M, Sikkel M, Paur H, Benard L . Plasticity of surface structures and β(2)-adrenergic receptor localization in failing ventricular cardiomyocytes during recovery from heart failure. Circ Heart Fail. 2012; 5(3):357-65. PMC: 4886822. DOI: 10.1161/CIRCHEARTFAILURE.111.964692. View