期刊文献+

大鼠耳蜗发育过程中生存素和半胱氨酸天冬氨酸蛋白酶3的表达

Expression of survivin and caspase-3 during the development process in rat cochlea
原文传递
导出
摘要 目的探讨大鼠耳蜗形态学发育过程中凋亡相关因素的作用。方法通过免疫组化蛋白定位以及逆转录一聚合酶链反应(RT-PCR)技术检测生存素(survivin)和半胱氨酸天冬氨酸蛋白酶3(caspase-3)在胚胎期及出生后Wistar大鼠耳蜗中的表达情况。结果survivin和caspase-3在细胞增殖期广泛表达于即将分化发育形成Corti器的蜗管底壁,在细胞分化期表达逐渐增强;survivin在细胞分化末期达到高峰,持续到细胞发育成熟期开始之后下降,在成熟的corti器毛细胞中仍有较强表达;而caspase-3在细胞发育成熟期开始时达到高峰,以后逐渐下降,直至表达消失。结论survivin和caspase-3在大鼠耳蜗发育过程中表达范围相似,但表达量在时间上并不同步,survivin的表达高峰早于caspase-3,二者相互作用共同调控细胞凋亡,促进耳蜗形态结构的成熟。 Objective To explore the role of some apoptosis regulators during the development in rat cochlea. Methods The morphological development process of cochlea was observed in Wistar rat aged between embryo day 13 to postnatal day 14 in this experiment. Survivin and caspase-3 were respectively detested at protein and mRNA levels by immunohistochemistry and reverse transcription polymerase chain reaction(RT-PCR). Results The expression of survivin and caspase-3 located in the bottom wall of the cochlear duct. Not only they widespread in the cell proliferation, but also they gradually enhanced in the cell differentiation. Both of them had a crest-time, and survivin was prior to caspase-3. In organ of corti during adult time, caspase-3 was not present and survivin was only expressed. Conclusions During the development of the rat cochlea, both of them had similar location and trend. But they were derangement. This showed that both of them participated in the cochlear morphological development. It was suggested that the interaction between survivin and caspas-3 regulated the apoptosis, promoted the cochlear morphological development.
出处 《中华耳鼻咽喉头颈外科杂志》 CAS CSCD 北大核心 2008年第9期686-690,共5页 Chinese Journal of Otorhinolaryngology Head and Neck Surgery
关键词 耳蜗 器官发生 生存素 半胱氨酸天冬氨酸蛋白酶3 细胞凋亡 Cochlea Organogenesis Survivin Caspase-3 Apoptosis
  • 相关文献

参考文献13

  • 1Swanson GJ. Regeneration of sensory hair cells in the vertebrate inner ear. Trends Neurosci, 1988, 11:339-342.
  • 2Nikolic P, Jarlebark LE, Billett TE, et al. Apoptosis in the developing rat cochlea and its related structures. Brain Res Dev Brain Res, 2000, 119:75-83.
  • 3Lang H, Bever MM, Fekete DM. Cell proliferation and cell death in the developing chick inner ear: spatial and temporal patterns. J Comp Neurol, 2000, 417:205-220.
  • 4Leon Y, Sanchez-Galiano S, Gorospe L Programmed cell death in the development of the vertebrate inner ear. Apoptosis, 2004, 9 : 255 -264.
  • 5刘少锋,周梁,李华伟.细胞增殖及凋亡与耳蜗感觉上皮的分化[J].听力学及言语疾病杂志,2004,12(4):252-253. 被引量:3
  • 6Hatch EP, Noyes CA, Wang X, et al. Fgf3 is required for dorsal patterning and morphogenesis of the inner ear epithelium. Development, 2007, 134: 3615-3625.
  • 7Ohyama T, Mohamed OA, Taketo MM, et al. Wnt signals mediate a fate decision between ofic plaeode and epidermis. Development, 2006, 133: 865-875.
  • 8Martin K, Groves AK. Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otlc placode induction. Development, 2006, 133: 877-887.
  • 9Lopez-Schier H, Hudspeth AT. A two-step mechanism underlies the planar polarization of regenerating sensory hair cells. Proc Natl Acad Sci U S A, 2006,103:18615-18620.
  • 10Morishita H, Makishima T, Kaneko C, et al. Deafness due to degeneration of cochlear neurons in easpase-3-deflcient mice. Biochem Biophys Res Commun, 2001,284:142-149.

二级参考文献27

  • 1Kawasaki H, Toyoda M, Shinohara H, et al. Expression of surviving correlates with apoptosis,proliferation, and angiogenesis during human colorectal tumorigenesis. Cancer, 2001,91 ( 11 ): 2026-2032.
  • 2Satoh K, Kaneko K, Hirota M, et al. Expression of survivin is correlated with cancer cell apoptosis and is involved in the development of human pancreatic duct cell tumors. Cancer,2001,92(2) :271-278.
  • 3Allen SM, Florell SR, Hanks AN,et al. Survivin expression in mouse skin prevents papilloma regression and promotes chemical-induced tumor progression. Cancer Res,2003,63(3) :567-572.
  • 4Islam A, Kagetama H, Takada N, et al. High expression of survivin,mapped to 17q25, is significantly associated with poor prognostri factors and promotes cell survival in human neuroblastoma. Oncogene, 2000,19(5) :617-623.
  • 5Wall NR,Connor DS,Plescia J,et al. Suppression of survivin phosphorylation on Thr34 by flavopiridol enhances tumor cell apoptosis. Cancer Res,2003,63(1) :230-235.
  • 6Ikeguchi M, Ueda T, Sakatni T, et al. Expression of survivin messenger RNA correlates with poor prognosis in patient with hepatocellular carcinoma. Diagn Mol Pathol, 2002,11 ( 1 ): 33-40.
  • 7Sharp JD, Hausladen DA, Maher MG, et al. Bladder cancer detection with urinary surviving, an inhibitor of apoptosis. Frontier in Bioscience,2002,1: 36-42.
  • 8Bao R, Connolly DC, Murphy M,et al. Activation of cencer-specific gene expression by the survivin promoter. J Natl Caner Inst, 2002,94 (7):522-528.
  • 9Olie RA, Simoes-Wust AP, Baumann B, et al. A novel antisense oligonucleotide targeting surviving expression induces apoptosis and sensitizes lung cancer cells to chemotherapy. Cancer Res,2000,60(11):2805-2809.
  • 10Wall NR, Connor DS, Plescia J, et al. Suppression of survivin phosphorylation on Thr34 by flavopiridol enhances tumor cell apoptosis. Cancer Res,2003,63(1): 230-235.

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部