SERCA

SERCA, or sarco/endoplasmic reticulum Ca2+-ATPase, or SR Ca2+-ATPase, is a calcium ATPase-type P-ATPase. Its major function is to transport calcium from the cytosol into the sarcoplasmic reticulum.

Function

SERCA is a P-type ATPase.[1] It resides in the sarcoplasmic reticulum (SR) within myocytes.[1] It is a Ca2+ ATPase that transfers Ca2+ from the cytosol of the cell to the lumen of the SR.[1] This uses energy from ATP hydrolysis during muscle relaxation.[1]

There are 3 major domains on the cytoplasmic face of SERCA: the phosphorylation and nucleotide-binding domains, which form the catalytic site, and the actuator domain, which is involved in the transmission of major conformational changes.

It seems that, in addition to the calcium-transporting properties, SERCA1 generates heat in some adipocytes [2][3] and can improve cold tolerance in some wood frogs.[4]

Regulation

The rate at which SERCA moves Ca2+ across the SR membrane can be controlled by the regulatory protein phospholamban (PLB/PLN). SERCA is not as active when PLB is bound to it. Increased β-adrenergic stimulation reduces the association between SERCA and PLB by the phosphorylation of PLB by PKA.[5] When PLB is associated with SERCA, the rate of Ca2+ movement is reduced; upon dissociation of PLB, Ca2+ movement increases.

Another protein, calsequestrin, binds calcium within the SR and helps to reduce the concentration of free calcium within the SR, which assists SERCA so that it does not have to pump against such a high concentration gradient. The SR has a much higher concentration of Ca2+ (10,000x) inside when compared to the cytoplasmic Ca2+ concentration. SERCA2 can be regulated by microRNAs, for instance miR-25 suppresses SERCA2 in heart failure.

For experimental purposes, SERCA can be inhibited by thapsigargin and induced by istaroxime.

Paralogs

There are 3 major paralogs, SERCA1-3, which are expressed at various levels in different cell types.

There are additional post-translational isoforms of both SERCA2 and SERCA3, which serve to introduce the possibility of cell-type-specific Ca2+-reuptake responses as well as increasing the overall complexity of the Ca2+ signaling mechanism.

References
  1. Marín-García, José (2014-01-01), Marín-García, José (ed.), "Chapter 23 - Gene- and Cell-Based Therapy for Cardiovascular Disease", Post-Genomic Cardiology (Second Edition), Boston: Academic Press, pp. 783–833, doi:10.1016/b978-0-12-404599-6.00023-8, ISBN 978-0-12-404599-6, retrieved 2020-12-28
  2. de Meis L; Oliveira GM; Arruda AP; Santos R; Costa RM; Benchimol M (2005). "The thermogenic activity of rat brown adipose tissue and rabbit white muscle Ca2+-ATPase". IUBMB Life. 57 (4–5): 337–45. doi:10.1080/15216540500092534. PMID 16036618.
  3. Arruda AP; Nigro M; Oliveira GM; de Meis L (June 2007). "Thermogenic activity of Ca2+-ATPase from skeletal muscle heavy sarcoplasmic reticulum: the role of ryanodine Ca2+ channel". Biochim. Biophys. Acta. 1768 (6): 1498–505. doi:10.1016/j.bbamem.2007.03.016. PMID 17466935.
  4. Dode, L; Van Baelen, K; Wuytack, F; Dean, WL (2001). "Low temperature molecular adaptation of the skeletal muscle sarco(endo)plasmic reticulum Ca2+-ATPase 1 (SERCA 1) in the wood frog (Rana sylvatica)". Journal of Biological Chemistry. 276 (6): 3911–9. doi:10.1074/jbc.m007719200. PMID 11044449.
  5. MacLennan, David H.; Kranias, Evangelia G. (July 2003). "Phospholamban: a crucial regulator of cardiac contractility". Nature Reviews Molecular Cell Biology. 4 (7): 566–577. doi:10.1038/nrm1151. PMID 12838339.
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