Ryanodine receptor and junctional membrane structure

Folia Pharmacologica Japonica

Volumn 121, Issue 4, 2003, Pages 203-210

  Takeshima, Hiroshi ^a  

^a TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Ca2+ signaling; Intracellular Ca2+ store; Junctional membrane structure; Junctophilin; Ryanodine receptor

Indexed keywords

1,4 DIHYDROPYRIDINE RECEPTOR; CALCIUM CHANNEL; CALCIUM ION; COMPLEMENTARY DNA; COMPLEMENTARY RNA; FK 506 BINDING PROTEIN; RECEPTOR SUBTYPE; RYANODINE RECEPTOR; TACROLIMUS;

ANIMAL CELL; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; CELL MEMBRANE; CELL TYPE; EMBRYO; ENDOPLASMIC RETICULUM; HUMAN; HUMAN CELL; KNOCKOUT GENE; MEMBRANE STRUCTURE; MOUSE; NEWBORN; NONHUMAN; PHENOTYPE; REVIEW; SARCOPLASMIC RETICULUM; TISSUE DISTRIBUTION;

CALCIUM; CALCIUM CHANNELS; ENDOPLASMIC RETICULUM; HUMANS; MEMBRANE PROTEINS; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL; SARCOPLASMIC RETICULUM;

EID: 0037256663     PISSN: 00155691     EISSN: None     Source Type: Journal    
DOI: 10.1254/fpj.121.203     Document Type: Review

References (40)

1. Endo M, Tanaka M and Ogawa Y: Calcium induced release of calcium from the sarcoplasmic reticulum of skinned skeletal muscle fibres. Nature 319, 600-602 (1970)
2. 2+ release channels and their regulation by endogenous effectors. Annu Rev Physiol 56, 485-508 (1994)
3. Inui M, Saito A and Fleischer S: Isolation of the ryanodine receptor from cardiac sarcoplasmic reticulum and identity with the feet structures. J Biol Chem 262, 15637-15642 (1987)
4. 2+-permeable pore of the calcium release channel. J Biol Chem 262, 16636-16643 (1987)
5. Franzini-Armstrong C: Freeze-fracture of frog slow tonic fibers. Structure of surface and internal membranes. Tissue Cell 16, 146-166 (1984)
6. Takeshima H, Nishimura S, Matsumoto T, Ishida H, Kangawa K, Minamino N, Matsuo H, Ueda M, Hanaoka M, Hirose T, et al: Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. Nature 339, 439-445 (1989)
7. Nakai J, Imagawa T, Hakamata Y, Sigekawa M, Takashima H and Numa S: Primary structure and functional expression from cDNA of the cardiac ryanodine receptor / calcium release channel. FEBS Lett 271, 169-177 (1990)
8. Hakamata Y, Nakai J, Takeshima H and Imoto K: Primary structure and distribution of a novel ryanodine receptor/calcium release channel from rabbit brain. FEBS Lett 312, 229-235 (1992)
9. Brillantes AB, Ondrias K, Scott A, Kobrinsky E, Ondriasova E, Moschella MC, Jayaraman T, Landers M, Ehrlich BE and Marks AR: Stabilization of calcium release channel (ryanodine receptor) function by FK506-binding protein. Cell 77, 513-523 (1994)
10. Eu JP, Sun J, Xu L, Stamler JS and Meissner G: The skeletal muscle calcium release channel: coupled O2 sensor and NO signaling functions. Cell 102, 499-509 (2000)
11. Marx SO, Reiken S, Hisamatsu Y, Jayaraman T, Burkhoff D, Rosemblit N and Marks AR: PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor); defective regulation in failing hearts. Cell 101, 365-376 (2000)
12. Orlova EV, Serysheva II, van Heel M, Hamilton SL and Chiu W: Two structural configurations of the skeletal muscle calcium release channel. Nat Struct Biol 3, 547-552 (1996)
13. Furuichi T, Furutami D, Hakamata Y, Nakai J, Takeshima H and Mikoshiba K: Multiple types of ryanodine receptor/calcium release channels are differentially expressed in rabbit brain. J Neurosci 14, 4794-4805 (1994)
14. Schneider MF and Chandler WK: Voltage dependent charge movement of skeletal muscle: a possible step in excitation-contraction coupling. Nature 242, 244-246 (1973)
15. Block BA, Imagawa T, Campbell KP and Franzini-Armstrong C: Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle. J Cell Biol 107, 2587-2600 (1988)
16. Numa S, Tanabe T, Takeshima H, Mikami A, Niidome T, Nishimura S, Adams BA and Beam KG: Molecular insights into excitation-contraction coupling. Cold Spring Harbor Symp Quant Biol 45, 1-7 (1990)
17. Takeshima H, Iino M, Takekura H, Nishi M, Kuno J, Minowa O, Takano H and Noda T: Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene. Nature 369, 556-559 (1994)
18. Takekura H, Nishi M, Noda T, Takeshima H and Franzini-Armstrong C: Abnormal junctions between surface membrane and sarcoplasmic reticulum in skeletal muscle with a mutation targeted to the ryanodine receptor. Proc Natl Acad Sci USA 92, 3381-3385 (1995)
19. Nakai J, Dirksen RT, Nguyen HT, Pessah IN, Beam KG and Allen PD: Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor. Nature 380, 72-75 (1996)
20. 2+ current facilitation in skeletal muscle of transgenic mice lacking the ryanodine receptor type 1. J Physiol 496, 339-345 (1996)
21. 2+ release mechanism in the sarcoplasmic reticulum of the muscle from a patient with malignant hyperthermia. Biomed Res 4, 83-92 (1983)
22. 2+ release channel of skeletal sarcoplasmic reticulum is responsible for hypersensitivity to caffeine and halothane in malignant hyperthermia. J Biol Chem 269, 9413-9415 (1994)
23. 2+ regulation defects. Physiol Rev 76, 537-592 (1996)
24. Lopez-Lopez JR, Shacklock PS, Balke CW and Wier WG: Local calcium transients triggered by single L-type calcium channel currents in cardiac cells. Science 268, 1042-1045 (1995)
25. Verkhratsky A and Shmigol A: Calcium-induced calcium release in neurones. Cell Calcium 19, 1-14 (1996)
26. Takeshima H, Komazaki S, Hirose K, Nishi M, Noda T and Iino M: Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2. EMBO J 17, 3309-3316 (1998)
27. Ikemoto T, Komazaki S, Takeshima H, Nishi M, Noda T, Iino M and Endo M: Functional and morphological features of skeletal muscle from mutant mice lacking both type 1 and type 3 ryanodine receptors. J Physiol 501, 305-312 (1997)
28. Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, DeSimone L, Coltorti F, Bloise R, Keegan R, et al: Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Circulation 106, 69-74 (2002)
29. 2+ release in myocytes from dyspedic mice lacking type-1 ryanodine receptor. EMBO J 14, 2999-3006 (1995)
30. Takeshima H, Ikemoto T, Nishi M, Nishiyama N, Shimuta M, Sugitani Y, Kuno J, Saito I, Saito H, Endo M, et al: Generation and characterization of mutant mice lacking ryanodine receptor type 3. J Biol Chem 271, 19649-19652 (1996)
31. Bertocchini F, Ovitt CE, Conti A, Barone V, Schoeler HR, Bottinelli R, Reggiani C and Sorrentino V: Requirement for the ryanodine receptor type 3 for efficient contraction in neonatal skeletal muscles. EMBO J 16, 6956-6963 (1997)
32. Komazaki S, Ikemoto T, Takeshima H, Iino M, Endo M and Nakamura H: Morphological abnormalities of adrenal grand and hypertrophy of liver in mutant mice lacking ryanodine receptors. Cell Tissue Res 294, 467-473 (1998)
33. Takekura H, Takeshima H, Nishimura S, Takahashi M, Tanabe T, Flockerzi V, Hofmann F and Franzini-Armstrong C: Co-expression in CHO cells of two muscle protein involved in excitation-contraction coupling. J Muscle Res Cell Motil 16, 465-480 (1995)
34. Takeshima H, Komazaki S, Nishi M, Iino M and Kangawa K: Junctophilins: a novel family of junctional membrane complex proteins. Mol Cell 6, 11-22 (2000)
35. Nishi M, Mizushima A, Nakagawara K and Takeshima H: Characterization of human junctophilin subtype genes. Biochem Biophys Res Commun 273, 920-927 (2000)
36. Ito K, Komazaki S, Sasamoto K, Yoshida M, Nishi M, Kitamura K and Takeshima H: Deficiency of triad junction and contraction in mutant skeletal muscle lacking junctophilin type 1. J Cell Biol 154, 1059-1068 (2001)
37. 2+ store in embryonic cardiac myocytes. Front Biosci 7, d1642-1652 (2002)
38. Nishi M, Hashimoto K, Kuriyama K, Komazaki S, Kano M, Shibata S and Takeshima H: Motor discoordination in mutant mice lacking junctophilin type 3. Biochem Biophys Res Commun 292, 318-324 (2002)
39. Holmes SE, O'Hearn E, Rosenblatt A, Callahan C, Hwang HS, Ingersoll-Ashworth RG, Fleisher A, Stevanin G, Brice A, Potter NT, et al: A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2. Nat Genet 29, 377-378 (2001)