Passage of 17 kDa calmodulin through gap junctions of three vertebrate species

Tissue and Cell

Volumn 39, Issue 5, 2007, Pages 303-309

  Curran, J E ^a   Woodruff, R I ^a  

^a WEST CHESTER UNIVERSITY   (United States)

Author keywords

CaM; Gap junctions; Microinjection; Pore size

Indexed keywords

CALMODULIN; DYE; OCTANOL;

ANIMAL CELL; ARTICLE; CELL COMMUNICATION; CONTROLLED STUDY; CYTOPLASM; DOWN REGULATION; EPITHELIUM CELL; FEMALE; FLUORESCENCE; GAP JUNCTION; MICROINJECTION; MOLECULAR WEIGHT; NONHUMAN; OOCYTE; ORYZIAS; OVARY FOLLICLE; SIGNAL TRANSDUCTION; VERTEBRATE; XENOPUS LAEVIS; ZEBRA FISH;

AMPHIBIA; DANIO RERIO; ORYZIAS LATIPES; ORYZIINAE; TELEOSTEI; VERTEBRATA; XENOPUS LAEVIS;

EID: 34848926248     PISSN: 00408166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tice.2007.06.002     Document Type: Article

References (61)

1. Adler E.L., and Woodruff R.I. Varied effects of 1-octanol on gap junctional communication between ovarian epithelial cells and oocytes of Oncopeltus fasciatus, Hyalophora cecropia and Drosophila melanogaster. Arch. Insect. Biochem. Physiol. 42 (2000) 22-32
2. Ahmad S., Martin P.E., and Evans W.H. Assembly of gap junction channels: mechanism, effects of calmodulin antagonists and identification of connexin oligomerization determinants. Euro. J. Biochem. 268 16 (2001) 4544-4552
3. Anderson K.L., and Woodruff R.I. A gap junctionally transmitted epithelial cell signal regulates endocytic yolk uptake in Oncopeltus fasciatus. Devel. Biol. 239 1 (2001) 68-78
4. Anderson L. Protein synthesis and uptake by isolated Cecropia oocytes. J. Cell Sci. 8 (1971) 735-750
5. Anderson L.M., and Telfer W.H. A follicle cell contribution to the yolk spheres of moth oocytes. Tissue Cell 1 (1969) 633-644
6. Andreuccetti P., Iodice M., Presco M., and Gualtieri R. Intercellular bridges between granulosa cells and the oocyte in the Elasmobranch Raya asterias. Anat. Record. 255 (1999) 180-187
7. Babu Y.S., Bugg C.E., and Cook W.J. In: Calmodulin, Cohen P., and Klee C.B. (Eds). Three-Dimensional Structure of Calmodulin (1988), Elsevier Science Publishers, Amsterdam 83-89
8. Berdan R.C. Intercellular communication in arthropods. Biophysical, ultrastructural and biochemical approaches. In: De Mello W.C. (Ed). Cell-To-Cell Communication (1987), Plenum, New York 299-370
9. Blodow A., Ngezahayo A., Ernst A., and Kolb H.A. Calmodulin antagonists suppress gap junction coupling in isolated Hensen cells of the guinea pig cochlea. Pflugers Arch. 446 1 (2003) 36-41
10. Brooks R.A., and Woodruff R.I. Calmodulin transmitted through gap junctions stimulates endocytic incorporation of yolk precursors in insect oocytes. Dev. Biol. 271 (2004) 339-349
11. Brown C.L., and Wiley H.S. Oocyte-follicle cell gap junctions in Xenopus laevis and the effects of gonadotropin on their permeability. Science 203 (1978) 182-183
12. Browne C.L., and Werner W. Intercellular junctions between follicle cells and oocytes of Xenopus laevis. J. Exp. Zool. 230 (1984) 105-113
13. Dale B., Santella L., and Tosti E. Gap-junctional permeability in early and cleavage-arrested ascidian embryos. Development 112 1 (1991) 153-160
14. De Pina-Benabou M.H., Srinivas M., Spray D.C., and Scemes E. Calmodulin kinase pathway mediates the K+-induced increase in Gap junctional communication between mouse spinal cord astrocytes. J. Neruorsci. 21 17 (2001) 6635-6643
15. Dumont J.N. Oogenesis in Xenopus laevis (Daudin). 1. Stages of oocyte development n laboratory maintained animals. J. Morph. 136 (1972) 153-180
16. Flagg-Newton J., Simpson I., and Loewenstein W.R. Permeability of the cell-to-cell membrane channels in mammalian cell junction. Science 205 4404 (1979) 404-407
17. Gho M. Voltage-clamp analysis of gap junctions between embryonic muscles in Drosophila. J. Physiol. 481 2 (1994) 371-383
18. Haeseleer F., and Palczewski K. Calmodulin and Ca2+-binding proteins (CaBPs): variations on a theme. Adv. Exp. Med . Biol. 514 (2002) 303-317
19. 2+ release. FEBS Lett. 449 1 (1999) 70-74
20. Hausman S.J., Anderson L.M., and Telfer W.H. The dependence of cecropia yolk formation in vitro on specific blood proteins. J. Cell Biol. 48 (1971) 303-313
21. Hoh J.H., Sosinsky G.E., Revel J.P., and Hansma P.K. Structure of the extracellular surface of the gap junction by atomic force microscopy. Biophys. J. 24 (1993) 5-12
22. Inagaki N., Suzuki S., Kitai H., Nakatogawa N., Kuji N., Iwahashi K., and Yoshimura Y. Effect of KN-62, a selective inhibitor of calmodulin-dependent kinase II, on mouse oocyte activation. J. Assist. Reprod. Genet. 14 10 (1997) 609-616
23. Ito J., Kaneko R., and Hirabayashi M. The regulation of calcium/calmodulin-dependent protein kinase II during oocyte activation in the rat. J. Reprod. Dev. 52 3 (2006) 436-447
24. Ito J., Kawano N., Hirabayashi M., and Shimada M. The role of calcium/calmodulin-dependent protein kinase II on the inactivation of MAP kinase and p34cdc2 kinase during fertilization and activation in pig oocytes. Reproduction 128 4 (2004) 409-415
25. Ishida H., and Vogel H.J. Protein-peptide interaction studies demonstrate the versatility of calmodulin target protein binding. Protein Pept. Lett. 13 (2006) 455-465
26. Iwamatsu T., Ohta T., Oshima E., and Sakai N. Oogenesis in the Medaka, Oryzias latipes - Stages of oocyte development. Zoo. Sci. 5 (1988) 353-373
27. Kessel R.G., Tung H.N., Roberts R., and Beams H.W. The presence and distribution of gap junctions in the oocyte-follicle cell complex of the zebrafish, Brachydanio rerio. Submicro. Cytol. 17 2 (1985) 239-253
28. Klee C.B., Crouch T.H., and Richman P.G. Calmodulin. Annu. Rev. Biochem. 49 (1980) 489-515
29. Kondo T., Kotani T., and Yamashita M. Dispersion of Cyclin B mRNA aggregation is coupled with transitional activation of the mRNA during zebrafish oocyte maturation. Dev. Biol. 229 (2001) 421-431
30. Korfsmeier K.-H. PCNA in the ovary of zebrafish (Brachydanio rerio, Ham. -Buch). ACTA Histo. Chem. 104 (2002) 73-76
31. Kumar N.M., and Gilula N.B. The gap junction communication channel. Cell 84 3 (1996) 381-388
32. Kwon H.B., and Ahn R.S. Relative roles of theca and granulosa cells in ovarian follicular steroidogenesis in the amphibian, Rana nigromaculata. Gen. Comp. Endocrinol. 94 (1994) 207-214
33. Lacy M.P., McIntosh R.P., and McIntosh J.E. Angiotensisn II stimulates an endogenous response in Xenopus ovarian follicles. Biochem. Biophys. Res. Comm. 159 (1989) 658-663
34. Lal R., John S.A., Laird D.W., and Arnsdorf M.F. Heart gap junction preparations reveal hemiplaques by atomic force microscopy. Am. J. Physiol. Cell Physiol. 268 (1995) C968-C977
35. Lurtz M.M., and Louis C.F. Calmodulin and protein kinase C regulate gap junctional coupling in lens epithelial cells. Am. J. Physiol. Cell Physiol. 285 (2003) C1475-C1482
36. Nutt L.K., Margolis S.S., Jensen M., Herman C.E., Dunphy W.G., Rathmell J.C., and Kornbluth S. Metabolic regulation of oocyte cell death through the CaMKII-mediated phosphorylation of caspase-2. Cell 123 1 (2005) 89-103
37. Pan M., Bell W., and Telfer W. Vitellogenic blood protein synthesis by insect fat body. Science 165 (1969) 393-394
38. Patiño R., and Purkiss R.T. Inhibitory effects of n-alkanols on the hormonal induction of maturation in follicle-enclosed Xenopus oocytes: implications for gap junctional transport of maturation-inducing steroid. Gen. Comp. Endocrinol. 91 (1993) 189-198
39. Peracchia C., Bernardin G., and Peracchia L.L. Is calmodulin involved in the regulation of gap junction permeability?. Pflug. Arch. 399 (1983) 152-154
40. Peracchia C., Sotkis A., Wang X.G., Peracchia L.L., and Persechin A. Calmodulin Directly Gates Gap Junction Channels. J. Biol. Chem. 275 34 (2000) 26220-26224
41. Peracchia C., Wang X.G., and Peracchia L.L. Slow gating of gap junction channels and calmodulin. J. Membr. Biol. 178 (2000) 55-70
42. Pitt G.S. Calmodulin and CaMKII as molecular switches for cardiac ion channels. Cardiovasc. Res. 73 4 (2007) 641-647
43. 2+/calmodulin- dependent protein kinase II. Euro. J. Biochem. 192 (1990) 263-273
44. Schuetz A.W., and Lessman C. Evidence for follicle wall involvement in ovulation and progesterone production in frog (Rana pipiens) follicles in vitro. Differention 22 (1982) 79-84
45. Schwarzmann G., Wiegandt H., Rose B., Zimmerman A., Ben-Haim D., and Loewenstein W.R. Diameter of the cell-to-cell junctional membrane channels as probed with neutral molecules. Science 213 4507 (1981) 551-553
46. Selman K., Wallace R.A., Sarka A., and Qi X. Stages of oocyte development in the Zebrafish, Brachydanio rerio. J. Morph. 218 (1993) 203-224
47. Simpson I., Rose B., and Loewenstein W.R. Size limit for molecules permeating the junctional membrane channels. Science 195 (1977) 294-296
48. Spray D.C., Cherbas L., Cherbas P., Morales E.A., and Carrow G.M. Ionic coupling and mitotic synchrony of siblings in a Drosophila cell line. Exp. Cell Res. 184 2 (1989) 509-517
49. Suchyna T.M., Nitsche J.M., Chilton M., Harris A.L., Veenstra R.D., and Nicholson B.J. Different ionic selectivities for connexins 26 and 32 produce rectifying gap junction channels. Biophys. J. 77 6 (1999) 2968-2987
50. Tucciarone L.M., and Lanclos K.D. Effect of calmodulin inhibitor, Stelazine, on the endocytosis of vitellogenin and transglutaminase activity in Xenopus laevis oocytes. Mol. Cell. Biochem. 45 (1982) 159-161
51. Waksmonski S.L., and Woodruff R.I. For uptake of yolk precursors, epithelial cell-oocyte gap junctional communication is required by insects representing six different orders. J. Insect Physiol. 48 (2002) 667-675
52. Wallace R.A. Interactions Between Somatic Cells and the Growing Oocyte of Xenopus laevis. Current Problems in Germ Cell Differentiation (1983), Cambridge University Press
53. Wallace R.A., Jared D.W., Dumont J.N., and Sega M.W. Protein incorporation by isolated amphibian oocytes III. Optimum incubation conditions. J. Exp. Zool. 184 (1973) 321-334
54. Wallace R.A., and Misulovin Z. Long-term growth and differentiation in Xenopus oocytes in a defined medium. Proc. Nat'l. Acad. Sci. U. S. A. 75 (1978) 5534-5538
55. Wallace R.A., Misulovin Z., and Etkin L.D. Full-grown oocytes from Xenopus laevis resume growth when placed in culture. Proc. Natl. Acad. Sci. U. S. A. 78 (1981) 3078-3082
56. Weber P.A., Chang H.C., Spaeth K.E., Nitsche J.M., and Nicholson B.J. The permeability of gap junction channels to probes of different size is dependent on connexin composition and permeant-pore affinities. Biophys. J. 87 (2004) 958-973
57. Wiley H.S., and Dumont J.D. Stimulation of vitellogenin uptake in stage IV Xenopus oocytes by treatment with chorionic gonatotropin in vitro. Biol. Reprod. 17 (1978) 762-771
58. Woodruff R.I. Calmodulin transit via gap junctions is reduced in the absence of an electric field. J. Insect. Physiol. 51 (2005) 843-852
59. Woodruff R.I., Huebner E., and Telfer W.H. Ion currents in Hyalophora ovaries: The role of the epithelium and the intercellular spaces of the trophic cap. Dev. Biol. 117 (1986) 405-416
60. Woodruff R.I., and Tilney L.G. Intercellular bridges between epithelial cells in the Drosophila ovarian follicle: a possible aid to localized signaling. Dev. Biol. 200 (1998) 82-91
61. Yeager N. Structure of cardiac gap junction intercellular channels. J. Struct. Biol. 121 (1998) 231-245