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豚鼠耳蜗Hensen细胞的分离、活性鉴定及其胞内静态游离Ca^(2+)分布 被引量:4

ISOLATION, VIABILITY ASSESSMENT AND STATIC FREE Ca^(2+) DISTRIBUTION IN HENSEN CELL OF THE GUINEA PIG COCHLEA
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摘要 使用酶消化法及机械分离法对 Hensen细胞进行分离 ,置于倒置显微镜下用碘化丙啶及钙敏荧光染料 Fluo-3进行细胞活性鉴定并在激光扫描共聚焦显微镜下观察静息状态 Hensen细胞内的游离 Ca2 +的时空分布。结果证明 ,每个豚鼠耳蜗可以得到单离的 Hensen细胞 5~ 12个。细胞活性良好 ,可保持 5~ 6h。当细胞变性、坏死时可见一系列的形态学变化。对此得出几点判断 Hensen细胞活性的标准 :(1)细胞体呈卵圆形或椭圆形 ,大小可不一致 ;(2 )细胞膜完整 ,细胞边界清楚 ,折光现象明显 ;(3 )细胞浆清澈透明 ,无布朗运动 ,无溢出 ;(4 )细胞浆内的脂滴清晰可辨 ,折光现象明显 ;(5 )细胞无水肿 (即无气球样变 )。在静息状态下 ,Hensen细胞内的 Ca2 + 在细胞内分布不均匀 ,脂滴所在部位没有 Ca2 + 的分布。随时间延长 ,细胞内的 [Ca2 + ] i可小幅度振荡 ,但基本处于一种稳定状态。本工作为进一步对 Enzymatic and mechanical method was used to isolate Hensen's cell. The cell's viability was judged with propidium iodide and Fluo 3 under inverted microscope and then Ca 2+ distribution was observed in the cell with laser scan confocal microscope. We could get 5 to 12 Hensen's cells with good viability from each guinea pig cochlea. The viability could last 5 to 6 hours. There were a series of morphological changes when the cells underwent degeneration and necrosis. Some standards ccold be used for assessing the viability of Hensen's cell: (1) the shape of the cell body appeared to be oval round or ellipse and its boundary was clear; (2) the cell's membrane was intact with apparent refraction and without cytoplasm leaking out; (3) the fat droplets in the cytoplasm were conspicuous with apparent refraction. (4) there were small granulates in the cell distributed evenly in the cytoplasm, which might be organells. Under static situation, the Ca 2+ concentration was in a gradient from center to edge, high in the center and low on the edge. The [Ca 2+ ]i in Hensen's cell was in homeostatic state. This work set up a foundation for further study on the characteristic of Hensen's cell.
出处 《神经解剖学杂志》 CAS CSCD 北大核心 2002年第1期13-16,W005,共5页 Chinese Journal of Neuroanatomy
基金 国家自然科学基金 (No.3 0 0 70 812 )资助项目
关键词 Hensen细胞 细胞活性 形态学 耳蜗 豚鼠 分离 活性鉴定 胞内静态游离Ca^2+ 分布 Hensen cell, cell viability, morphology, cochlea, guinea pig
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参考文献9

  • 1Sugasawa M, Erostegui C, Blanchet C, et al. ATP activates a cation conductance and Ca2+-dependent Cl- conductence in Hensen cells of guinea pig cochlea. Am J Physiol, 1996,271(6Pt1):C1817~1827
  • 2Flock , Flock B, Fridberger A, et al. Supporting cells Contribute to control of hearing sensitivity. J Neurosci, 1999,19:4498~4501
  • 3Burgess BJ, Adams JC, Joseph B, et al. Morphologic evidence for innervation of Deiters' and Hensen's cells in the guinea pig. Hear Res, 1997,108:74~82
  • 4Forge A, Becker D, Casalotti S, et al. Gap junctions and connexin expression in the inner ear. Novartis Found Symp, 1999,219:134~150
  • 5Miguel A, Merchan JA, Ludena MD. Morphology of Hensen cells. J Anat, 1980,131:519~523
  • 6Zajic G, Schacht J. Comparison of isolated outer hair cells from five mammalian. Hear Res, 1987,26:249~256
  • 7Lenzi D, Roberts WM. Calcium signaling in hair cells: multiple roles in a compact cell. Curr Opin Neurobiol, 1994,4:496~502
  • 8Fessenden JD, Schacht J. Localization of soluble guanylate cyclase activity in the guinea pig cochlear suggests involvement in regulation of blood flow and supporting cell physiologty. J Histochem Cytochem, 1997,45:1401~1408
  • 9Tian F ,Fessenden JD,Schacht J. Cyclic GMP-dependent protein kinase-I in the guinea pig cochlea. Hear Res, 1999,131:63~70

同被引文献44

  • 1汪谦 主编.现代医学试验方法[M].北京: 人民卫生出版社,1997.211~230.
  • 2王尔贵 王锦玲 孟美鹃 等.爆震对豚鼠耳蜗和耳蜗神经cAMP的影响[J].中华耳鼻咽喉科杂志,1985,20:223-223.
  • 3Todt I, Ngazahayo A, Ernst A, et al. Hydrogen peroxide inhibits gap junctional coupling and modulates intracellular free calcium in cochlear Hensen cells. J Membr Biol,2001,181:107-114.
  • 4Chen C, Skellett BA, Fallon M,et al.Additional pharmacological evidence that endogenous ATP modulates cochlear mechanics.Hear Res, 1998,118 : 47-61.
  • 5Manley GA, Kirk DL, Koppl C, et al. In vivo evidence for a cochlear amplifier in the hair cell bundle of lizards. Proc Natl Acad Sci USA ,2001,98:2826-2831.
  • 6Dallos P. The active cochlea. J Neurosci,1992,12: 4575-4585.
  • 7Santos-Sacchi J. The effects of cytoplasmic acidification uponelectrical coupling in the organ of Corti. Hear Res, 1985,19:207-215.
  • 8Marcus DC,Sunese H,Liu J, et al. Protein kinase C mediates P2U purinergic receptor inhibition of K^+ channel in apical membrane of strial marginal cells.Hear Res,1998,115:82-92.
  • 9Dulon D, Moataz R, Mollard P. Characterization of Ca^2+ signals generated by extracellular nucleotides in supporting cells of the organ of Corti. Cell Calcium,1993,14:245-254.
  • 10Santos-Sacchi J. Isolated supporting cells from the organ of Corti:some whole cell electrical characteristics and estimates of gap junctional conductance.Hear Res ,1991,52:89-98.

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