Ca2+ and K+ (BK) channels in chick hair cells are clustered and colocalized with apical-basal and tonotopic gradients

被引:33
作者
Samaranayake, H
Saunders, JC
Greene, MI
Navaratnam, DS
机构
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
[3] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Philadelphia, PA 19104 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2004年 / 560卷 / 01期
关键词
D O I
10.1113/jphysiol.2004.069856
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Electrical resonance is a mechanism used by birds and many vertebrates to discriminate between frequencies of sound, and occurs when the intrinsic oscillation in the membrane potential of a specific hair cell corresponds to a specific stimulus sound frequency. This intrinsic oscillation results from an interplay between an inward Ca2+ current and the resultant activation of a hyperpolarizing Ca2+-activated K+ current. These channels are predicted to lie in close proximity owing to the fast oscillation in membrane potential. The interplay of these channels is widespread in the nervous system, where they perform numerous roles including the control of synaptic release, burst frequency and circadian rhythm generation. Here, we used confocal microscopy to show that these two ion channels are clustered and colocalized in the chick hair cell membrane. The majority of Ca2+ channels were colocalized while the proportion of colocalized BK channels was markedly less. In addition, we report both an apical-basal gradient of these clusters in individual hair cells, as well as a gradient in the number of clusters between hair cells along the tonotopic axis. These results give physical confirmation of previous predictions. Since the proportion of colocalized channels was a constant function of Ca2+ channels, and not of BK channels, these results suggest that their colocalization is determined by the former. The molecular mechanisms underpinning their clustering and colocalization are likely to be common to other neuronal cells.
引用
收藏
页码:13 / 20
页数:8
相关论文
共 50 条
[21]   Roles for Ca2+ and K+ channels in cancer cells exposed to the hypoxic tumour microenvironment [J].
Girault, Alban ;
Ahidouch, Ahmed ;
Ouadid-Ahidouch, Halima .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2020, 1867 (04)
[22]   Ca2+ activates Cl- but not K+ channels in NCM460 cells [J].
Jones, HM ;
Moyer, MP ;
Lance, P ;
Duffey, ME .
GASTROENTEROLOGY, 2001, 120 (05) :A527-A527
[23]   Ca2+ permeable K+ channels in the plasma membrane of Arabidopsis mesophyll cells. [J].
Romano, LA ;
Miedema, H ;
Assmann, SM .
PLANT PHYSIOLOGY, 1997, 114 (03) :993-993
[24]   Inhibition of voltage-gated K+ channels and Ca2+ channels by diphenidol [J].
Yuk-Man Leung ;
Kar-Lok Wong ;
Ka-Shun Cheng ;
Chang-Shin Kuo ;
Tzu-Hui Su ;
Yu-Wen Chen ;
Tzu-Hurng Cheng .
Pharmacological Reports, 2012, 64 :739-744
[25]   Inhibition of voltage-gated K+ channels and Ca2+ channels by diphenidol [J].
Leung, Yuk-Man ;
Wong, Kar-Lok ;
Cheng, Ka-Shun ;
Kuo, Chang-Shin ;
Su, Tzu-Hui ;
Chen, Yu-Wen ;
Cheng, Tzu-Hurng .
PHARMACOLOGICAL REPORTS, 2012, 64 (03) :739-744
[26]   MONITORING TRANSIENT Ca2+ DYNAMICS WITH LARGE-CONDUCTANCE Ca2+-DEPENDENT K+ CHANNELS AT ACTIVE ZONES IN FROG SACCULAR HAIR CELLS [J].
Sy, T. ;
Grinnell, A. D. ;
Peskoff, A. ;
Yazejian, B. .
NEUROSCIENCE, 2010, 165 (03) :715-722
[27]   Activation of BK channels in rat chromaffin cells requires summation of Ca2+ influx from multiple Ca2+ channels [J].
Prakriya, M ;
Lingle, CJ .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 84 (03) :1123-1135
[28]   Ca2+ activation properties of hslo Ca2+-activated K+ channels [J].
Krause, JD ;
Reinhart, PH .
BIOPHYSICAL JOURNAL, 1998, 74 (02) :A210-A210
[29]   Large conductance Ca2+-activated K+ (BK) channel:: Activation by Ca2+ and voltage [J].
Latorre, Ramon ;
Brauchi, Sebastian .
BIOLOGICAL RESEARCH, 2006, 39 (03) :385-401
[30]   EICOSANOIDS MODULATE APICAL CA-2+ DEPENDENT K+ CHANNELS IN CULTURED RABBIT PRINCIPAL CELLS [J].
LING, BN ;
WEBSTER, CL ;
EATON, DC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :F116-F126