|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Characterization of ryanodine receptor and Ca2+-ATPase isoforms in the thermogenic heater organ of blue marlin (Makaira nigricans)

Stanford University, Hopkins Marine Station, Pacific Grove, CA 93950,
USA
Present address: Occidental College, Los Angeles, CA 90041, USA
* Author for correspondence (e-mail: morriss{at}stanford.edu)
Accepted 21 November 2002
A thermogenic organ is found beneath the brain of billfishes (Istiophoridae), swordfish (Xiphiidae) and the butterfly mackerel (Scombridae). The heater organ has been shown to warm the brain and eyes up to 14°C above ambient water temperature. Heater cells are derived from extraocular muscle fibers and express a modified muscle phenotype with an extensive transverse-tubule (T-tubule) network and sarcoplasmic reticulum (SR) enriched in Ca2+-ATPase (SERCA) pumps and ryanodine receptors (RyRs). Heater cells have a high mitochondria content but have lost most of the contractile myofilaments. Thermogenesis has been hypothesized to be associated with release and reuptake of Ca2+. In this study, Ca2+ fluxes in heater SR vesicles derived from blue marlin (Makaira nigricans) were measured using fura-2 fluorescence. Upon the addition of MgATP, heater SR vesicles rapidly sequestered Ca2+. Uptake of Ca2+ was thapsigargin sensitive, and maximum loading ranged between 0.8 µmol Ca2+ mg-1 protein and 1.0 µmol Ca2+ mg-1 protein. Upon the addition of 10 mmol l-1 caffeine or 350 µmol l-1 ryanodine, heater SR vesicles released only a small fraction of the loaded Ca2+. However, ryanodine could elicit a much larger Ca2+ release event when the activity of the SERCA pumps was reduced. RNase protection assays revealed that heater tissue expresses an RyR isoform that is also expressed in fish slow-twitch skeletal muscle but is distinct from the RyR expressed in fish fast-twitch skeletal muscle. The heater and slow-twitch muscle RyR isoform has unique physiological properties. In the presence of adenine nucleotides, this RyR remains open even though cytoplasmic Ca2+ is elevated, a condition that normally closes RyRs. The fast Ca2+ sequestration by the heater SR, coupled with a physiologically unique RyR, is hypothesized to promote Ca2+ cycling, ATP turnover and heat generation. A branch of the oculomotor nerve innervates heater organs, and, in this paper, we demonstrate that heater cells contain large `endplate-like' clusters of acetylcholine receptors that appear to provide a mechanism for nervous control of thermogenesis.
Key words: ryanodine receptor, RyR, Ca2+-ATPase, SERCA, thermogenesis, heater organ, marlin, Makaira nigricans
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
D. C. F. da Costa and A. M. Landeira-Fernandez Thermogenic activity of the Ca2+-ATPase from blue marlin heater organ: regulation by KCl and temperature Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2009; 297(5): R1460 - R1468. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ruf and W. Arnold Effects of polyunsaturated fatty acids on hibernation and torpor: a review and hypothesis Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2008; 294(3): R1044 - R1052. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Hirata, T. Watanabe, J. Hatakeyama, S. M. Sprague, L. Saint-Amant, A. Nagashima, W. W. Cui, W. Zhou, and J. Y. Kuwada Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease Development, August 1, 2007; 134(15): 2771 - 2781. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Silva Thermogenic Mechanisms and Their Hormonal Regulation Physiol Rev, April 1, 2006; 86(2): 435 - 464. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Landeira-Fernandez, J. M. Morrissette, J. M. Blank, and B. A. Block Temperature dependence of the Ca2+-ATPase (SERCA2) in the ventricles of tuna and mackerel Am J Physiol Regulatory Integrative Comp Physiol, February 1, 2004; 286(2): R398 - R404. [Abstract] [Full Text] [PDF] |
||||