Sarcoplasmic Reticulum Function in Smooth Muscle

• Published in: Physiological reviews Vol. 90; no. 1; pp. 113 - 178
• Main Authors: Wray, Susan, Burdyga, Theodor
• Format: Journal Article
• Language: English
• Published: United States Am Physiological Soc 01.01.2010; American Physiological Society
• Subjects: Animals; Calcium; Calcium - physiology; Calcium Channels - physiology; Cells; Female; Humans; Hydrogen-Ion Concentration; Integrated approach; Male; Models, Theoretical; Muscle, Smooth - physiology; Muscular system; Physiology; Sarcoplasmic Reticulum - physiology; Sarcoplasmic Reticulum Calcium-Transporting ATPases - physiology
• ISSN: 0031-9333; 1522-1210; 1522-1210
• DOI: 10.1152/physrev.00018.2008

Department of Physiology, School of Biomedical Sciences, University of Liverpool, Liverpool, United Kingdom The sarcoplasmic reticulum (SR) of smooth muscles presents many intriguing facets and questions concerning its roles, especially as these change with development, disease, and modulation of physiological activity. The SR's function was originally perceived to be synthetic and then that of a Ca store for the contractile proteins, acting as a Ca amplification mechanism as it does in striated muscles. Gradually, as investigators have struggled to find a convincing role for Ca-induced Ca release in many smooth muscles, a role in controlling excitability has emerged. This is the Ca spark/spontaneous transient outward current coupling mechanism which reduces excitability and limits contraction. Release of SR Ca occurs in response to inositol 1,4,5-trisphosphate, Ca, and nicotinic acid adenine dinucleotide phosphate, and depletion of SR Ca can initiate Ca entry, the mechanism of which is being investigated but seems to involve Stim and Orai as found in nonexcitable cells. The contribution of the elemental Ca signals from the SR, sparks and puffs, to global Ca signals, i.e., Ca waves and oscillations, is becoming clearer but is far from established. The dynamics of SR Ca release and uptake mechanisms are reviewed along with the control of luminal Ca. We review the growing list of the SR's functions that still includes Ca storage, contraction, and relaxation but has been expanded to encompass Ca homeostasis, generating local and global Ca signals, and contributing to cellular microdomains and signaling in other organelles, including mitochondria, lysosomes, and the nucleus. For an integrated approach, a review of aspects of the SR in health and disease and during development and aging are also included. While the sheer versatility of smooth muscle makes it foolish to have a "one model fits all" approach to this subject, we have tried to synthesize conclusions wherever possible.