Expression of the GABAA receptor/chloride channel in murine spermatogenic cells

Histology and Histopathology

Volumn 26, Issue 1, 2011, Pages 95-106

  Kanbara, Kiyoto ^a   Mori, Yoshiaki ^b   Kubota, Takahiro ^b   Watanabe, Masahito ^c   Yanagawa, Yuchio ^d   Otsuki, Yoshinori ^a  

^a Department of Anatomy and Cell Biology ^*  (Japan)

^b OSAKA MEDICAL COLLEGE   (Japan)

^c OSAKA HEALTH SCIENCE UNIVERSITY   (Japan)

^d GUNMA UNIVERSITY   (Japan)

Author keywords

GABA; GABAA receptor subunit; Patch clamp; Spermatogenesis

Indexed keywords

MURINAE;

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; CHLORIDE CHANNEL; GLUTAMATE DECARBOXYLASE; GLUTAMATE DECARBOXYLASE 1; GLUTAMATE DECARBOXYLASE 2; GREEN FLUORESCENT PROTEIN; HYBRID PROTEIN; MESSENGER RNA; PRIMER DNA; PROTEIN SUBUNIT;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; CELL CULTURE; CONFOCAL MICROSCOPY; GENETICS; IMMUNOHISTOCHEMISTRY; MALE; METABOLISM; MOUSE; NUCLEOTIDE SEQUENCE; PATCH CLAMP; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SPERMATID; SPERMATOCYTE; SPERMATOGENESIS; SPERMATOZOON; TRANSGENIC MOUSE;

ANIMALS; BASE SEQUENCE; CELLS, CULTURED; CHLORIDE CHANNELS; DNA PRIMERS; GAMMA-AMINOBUTYRIC ACID; GLUTAMATE DECARBOXYLASE; GREEN FLUORESCENT PROTEINS; IMMUNOHISTOCHEMISTRY; MALE; MICE; MICE, INBRED BALB C; MICE, TRANSGENIC; MICROSCOPY, CONFOCAL; PATCH-CLAMP TECHNIQUES; PROTEIN SUBUNITS; RECEPTORS, GABA-A; RECOMBINANT FUSION PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SPERMATIDS; SPERMATOCYTES; SPERMATOGENESIS; SPERMATOZOA;

EID: 78651242183     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (48)

1. Abe H., Yanagawa Y., Kanbara K., Maemura K., Hayasaki H., Azuma H., Katsuoka Y., Yabumoto M. and Watanabe M. (2005). Epithelial localization of green fluorescent protein-positive cells in epididymis of the GAD67-GFP knock-in mouse. J. Androl. 26, 568-577.
2. Akinci M. K. and Schofield P. R. (1999). Widespread expression of GABAA receptor subunits in peripheral tissues. Neurosci. Res. 35, 145-153.
3. Barbin G., Pollard H., Gaiarsa J. L. and Ben-Ari Y. (1993). Involvement of GABAA receptors in the outgrowth of cultured hippocampal neurons. Neurosci. Lett. 152, 150-154.
4. Barnard E. A., Skolnick P., Olsen R. W., Mohler H., Sieghart W., Biggio G., Braestrup C., Bateson A. N. and Langer S. Z. (1998). International union of pharmacology. XV. Subtypes of γ-aminobutyric acidA receptors: Classification on the basis of subunit structure and receptor function. Pharmacol. Rev. 50, 291-313.
5. Bowery N. G. and Enna S. J. (2000). γ-aminobutyric acid (B) receptors: first of the functional metabotropic heterodimers. J. Pharmacol. Exp. Ther. 292, 2-7.
6. Breitbart H. (2002). Intracellular calcium regulation in sperm capacitation and acrosomal reaction. Mol. Cell Endcrinol. 187, 139-144.
7. Calogero A. E., Hall J., Fishel S., Green S., Hunter A. and D'Agata R. (1996). Effects of gamma-aminobutyric acid on human sperm motility and hyperactivation. Mol. Hum. Reprod. 2, 733-738.
8. Calver A. R., Robbins M. J., Cosio C., Rice S. Q. J., Babbs A. J., Hirst W. D., Boyfield I., Wood, M. D., Russell R. B., Price G. W., Couve A., Moss S. J and Pangalos M. N. (2001). The C-terminal domains of the GABAB receptor subunits mediate intracellular trafficking but are not required for receptor signaling. J. Neurosci. 21, 1203-1210.
9. Castelli M. P., Ingianni A., Stefanini E. and Gessa G. L. (1999). Distribution of GABAB receptor mRNAs in the rat brain and peripheral organs. Life Sci. 64, 1321-1328.
10. Costa E. (1998). From GABAA-receptor diversity emerges a unified vision of GABAergic inhibition. Annu. Rev. Pharmacol. Toxicol. 38, 321-350.
11. Darszon A., Labarca P., Nishigaki T. and Espinosa F. (1999). Ion channels in sperm physiology. Physiol. Rev. 79, 481-510.
12. 2+ in cerebellar granule cell precursors via depolarization: implications for proliferation. IUBMB Life 61, 496-503.
13. Doepner R. F., Geigerseder C., Frungieri M. B., Gonzalez-Calvar S. I., Calandra R. S., Raemsch R., Fohr K., Kunz L. and Mayerhofer A. (2005). Insights into GABA receptor signalling in TM3 Leydig cells. Neuroendocrinology. 81, 381-390.
14. Erdö S. L. and Wolff J. R. (1990). γ-Aminobutyric acid outside the mammalian brain. J. Neurochem. 54, 363-372.
15. A receptors involve downstream signal transduction pathways. Steroids 73, 906-913.
16. Geigerseder C., Doepner R. F., Thalhammer A., Krieger A. and Mayerhofer A. (2004). Stimulation of TM3 Leydig cell proliferation via GABA (A).receptors: a new role for testicular GABA. Reprod. Biol. Endocrinol. 13, 1-12.
17. Hagiwara S. and Kawa K. (1984). Calcium and potassium in spermatogenic cells dissociated from rat seminiferous tubules. J. Physiol. 356, 135-149.
18. Hayasaki H., Sohma Y., Kanbara K., Maemura K., Kubota T. and Watanabe M. (2006). A local GABAergic system within rat trigeminal ganglion cells. Eur. J. Neurosci. 23, 1-13.
19. B receptor in rat testis and sperm. Biochem. Biophys. Res. Commun. 283, 243-247.
20. B receptors. Arch. Androl. 48, 369-378.
21. Hu J. H., Na Y., Hua M. Y., Jie J., Fu Z. J., Jian F. and He G. L. (2004). Identification of glutamate receptors and transporters in mouse and human sperm. J. Androl. 25, 140-146.
22. B receptor subunit proteins during spermatogenesis in rat testis. J. Androl. 26, 485-493.
23. 2+ channel. Nature 439, 737-740.
24. László Á., Nádasy G. L., Monos E., Zsolnai B. and Erdö S. L. (1992). The GABAergic system in human female genital organs. In: GABA outside the CNS. Erdö S. L. (ed). Springer-Verlag. New York, NY. pp 183-197.
25. Lee M. A. and Storey B. T. (1986). Bicarbonate is essential for fertilization of mouse egg: mouse sperm require it to undergo the acrosome reaction. Biol. Reprod. 34, 349-356.
26. Liu H., Li S., Zhang Y., Yan Y. and Li Y. (2009). Dynamic regulation of glutamic and decarboxylase 65 gene expression in rat testis. Acta. Biochim. Biophys. Sin. 41, 545-553.
27. Maric D., Liu Q. Y., Maric I., Chaudry S., Chang Y. H., Smith S. V., Sieghart W., Fritschy J. M. and Barker J. L. (2001). GABA expression dominates neuronal lineage progression in the embryonic rat neocortex and facilitates neurite outgrowth via GABA (A). autoreceptor/Cl-channels. J. Neurosci. 21, 2343-2360.
28. Marty S., Berninger B., Carroll P. and Thoenen H. (1996). GABAergic stimulation regulates the phenotype of hippocampal interneurons through the regulation of brainderived neurotrophic factor. Neuron 16, 565-570.
29. McKerman R. M. and Whiting P. J. (1996). Which GABAA-receptor subtypes really occur in the brain? Trends Neurosci. 19, 139-143.
30. A receptors. Brain Res. Rev. 29, 196-217.
31. Meizel S. (1997). Amino Acid neurotransmitter receptor/chloride channels of mammalian sperm and the acrosome reaction. Biol. Reprod. 56, 569-574.
32. B receptors. Int. Rev. Neurobiol. 36, 97-223.
33. A receptor function by PKA and PKC in adult hippocampal neurons. J. Neurosci. 19, 674-683.
34. A receptor research. Synapse 21, 189-274.
35. Ritta M. N., Calamera J. C. and Bas D. E. (1998). Occurrence of GABA and GABA receptors in human spermatozoa. Mol. Hum. Reprod. 4, 769-773.
36. A-like receptor is involved in progesterone-induced acrosome reaction exocytosis in mouse spermatozoa. Biol. Reprod. 52, 373-381.
37. Shi Q. X., Yuan Y. Y. and Roldan E. R. (1997). γ-Aminobutyric acid (GABA). induces the acrosome reaction in human spermatozoa. Mol. Hum. Reprod. 3, 677-683.
38. Tamamaki N., Yanagawa Y., Tomioka R., Miyazaki J., Obata K. and Kaneko T. (2003). Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse. J. Comp. Neurol. 467, 60-79.
39. B receptors in rat growth plate chondrocytes: Activation of the GABA receptors promotes proliferation of mouse chondrogenic ATDC5 cells. Mol. Cell Biochem. 273, 117-126.
40. Tamura S., Watanabe M., Kanbara K., Yanagawa T., Watanabe K., Otsuki Y. and Kinoshita M. (2009). Expression and distribution of GABAergic system in rat knee joint synovial membrane. Histol. Histopathol. 24, 1009-1019.
41. Tillakaratne N. J. K., Erlander M. G., Collard M. W., Greif K. F. and Tobin A. J. (1992). Glutamate decarboxylases in nonneural cells of rat testis and oviduct: differential expression of GAD65 and GAD67. J. Neurochem. 58, 618-627.
42. Tillakaratne N. J. K., Medina-Kauwe L. and Gibson K. M. (1995). Gammaaminobutyric acid (GABA). metabolism in mammalian neural and nonneural tissues. Com. Biochem. Physiol. A. Physiol. 112 A, 247-263.
43. Wang F. Y., Watanabe M., Zhu R. M. and Maemura K. (2004). Charactereristic expression of gamma-aminobutyric acid and glutamate decarboxylase in rat jejunum and its relation to differentiation of epithelial cells. World J. Gastroenterol. 10, 3608-3611.
44. Watanabe M., Maemura K., Kanbara K., Tamayama T. and Hayasaki H. (2002). GABA and GABA receptors in the central nervous system and other organs. Int. Rev. Cytol. 213, 1-47.
45. Watanabe M., Maemura K., Oki K., Shiraishi N., Shibayama Y. and Katsu K. (2006). Gamma-aminobutyric acid (GABA) and cell proliferation: focus on cancer cells Histol. Histopathol. 21, 1135-1141.
46. Wolff J. R., Joó F. and Dames W. (1978). Plasticity in dendrites shown by continuous GABA administration in superior cervical ganglion of adult rat. Nature 274, 72-74.
47. Xiang Y. Y., Wang S., Liu M., Hirota J. A., Li J., Ju W., Fan Y., Kelly M. M., Ye B., Orser B., O'Byrne P. M., Inman M. D., Yang X. and Lu W. Y. (2007). A GABAergic system in airway epithelium is essential for mucus overproduction in asthma. Nat. Med. 13, 862-867.
48. Xilouri M. and Papazafiri P. (2006). Anti-apoptotic effects of allopregnanolone on P19 neurons. Eur. J. Neurosci. 23, 43-54.