期刊文献+

囊性纤维跨膜转导调控因子的基因克隆及在小鼠组织中的表达 被引量:1

Cystic fibrosis transmembrane conductance regulator gene expression in mouse tissues
下载PDF
导出
摘要 目的 :观察囊性纤维跨膜转导调控因子 (CFTCR)在小鼠不同组织中的表达及定位。方法 :采用RT -PCR的方法 ,设计两对引物 ,位于核苷酸第 1348~ 170 8之间 ,另一对引物为 β -actine,用来检测RNA是否完整。然后用抗CFTCR抗体 ,应用免疫组化方法检测其在牙胚组织中的定位。结果 :CFTCR在小鼠的14种组织中有表达 ,包括牙胚组织和骨组织。并且CFTCR在牙成釉细胞中高表达。结论 :本研究首次发现CFTCR在矿化的组织中包括牙齿的成釉细胞中高表达 。 AIM:To characterize (cystic fibrosis transmembrane conductance regulator,CFTCR) gene expression in different murine tissues and further verify localization of CFTCR.METHODS:CFTCR expression was evaluated by RT-PCR with primers spanning in the region between nucleotides 1 348 and 1 708.β-actin primers were used to assess the integrity of the RNA.Antibodies against the CFTCR were used to localize CFTCR in the tooth of mouse. RESULTS: CFTCR expression was seen in all 14 tissues examined.Positive staining for CFTCR was detected in ameloblast.CONCLUSION:This study shows that the CFTCR is ubiquitously expression in murine tissues and ameloblast.This is the first report that the CFTCR is expressed in mineralized tissues including tooth. Expression of CFTCR in tooth indicates that this ion channel may be important in the mineralization process of enamel.
出处 《牙体牙髓牙周病学杂志》 CAS 2003年第6期295-300,T001,共7页 Chinese Journal of Conservative Dentistry
关键词 小鼠 CFTCR 牙釉质 矿化 mouse CFTCR enamel mineralization
  • 相关文献

参考文献16

  • 1[1]Riordan JR.The cystic fibrosis transmembrane conductance regulator[J].Annu Rev Physiol,1993,55(Review):609
  • 2[2]Kunzelmann K,Schreiber R,CFTR. A regulator of channels[J].J Membrane Biol, 1999,168(1):1
  • 3[3]Gyomorey K,Yeger H,Ackerley C,Garami E and Bear CE.Expression of the channel C1C-Z in the murine small intestine epithelium[J].Am J physiol cell physiol, 2000,279(6):1787
  • 4[4]Brill SR,Ross KE,Davidow CJ,et al.Immunolocalization of ion transport proteins in human autosomal dominant polycystic kidney epithelial calls[J].Proc Natl Acad Sci USA,1996,93(19):10206
  • 5[5]Umar S,Scott,Sellin JH,et al.Murine colonic mucosa hyperproliferation. I. Elevated CFTR expression and enhanced cAMP-dependent Cl- secretion[J].Am J physiol gastrointest liver physiol,2000,278(5):753
  • 6[6]Sehgal A,Presente A,Engelhardt JF.Developmental expression patterns of CFTR in ferret tracheal surface airway and submucosal gland epithelial[J].Am J Respir Cell Mol Biol,1996,15(1):122
  • 7[7]Illek B,Fischer H,Machen TE.Genetic disorders of membrane transport Ⅱ. Regulation of CFTR by small molecules including HCO3-[J].Am J physiol,1998,275(6 pt 1):1221
  • 8[8]Trezise AE,Chambers JA,Wardle CJ,et al.Expression of the cystic fibrosis gene in human foetal tissues[J].Hum Mol Genet,1993,2(3):213
  • 9[9]Anderson MP,Berger HA,Rich DP,et al.Nucleoside triphosphates are required to open the CFTR chloride channels[J].Cell,1991,67(4):775
  • 10[10]Wright JT,Kiefer CL,Hall KI,et al.Abnormal enamel development in a cystic fibrosis transgenic mouse model[J].J Dent Res,1996,75(4):966

同被引文献36

  • 1Fernald GW, Roberts MW, Boat TF. Cystic fibrosis:a current review [ J ] . Pediatric Dentistry, 1990,12 (2) :72 - 78.
  • 2Arquitt CK, Boyd C, Wright JT. Cystic fibrosis transmembrane regulator gene (CFTR) is associated with abnormal enamel for- mation[ J]. J Dent Res, 2002,81 (7) :492 - 496.
  • 3Kerem B, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis[ J]. Science, 1989, 245(4922) : 1073 - 1080.
  • 4Rogan MP, Stoltz DA, Hornick DB. Cystic fibrosis transmem- brahe conductance regulator intracellular processing, trafficking, and opportunities for mutation - specific treatment [ J ]. Chest, 2011,139(6) :1480 - 1490.
  • 5Derichs N. Targeting a genetic defect: cystic fibrosis transmem- brane conductance regulator modulators in cystic fibrosis [ J ]. Eur Respir Rev , 2013,22(127) :58 -65.
  • 6Primosch RE. Tetracycline discoloration, enamel defects, and dental caries in patients with cystic fibrosis[ J. Oral Surg Oral Med Oral Pathol, 1980,50 (4) :301 - 308.
  • 7Jagels AE, Sweeney EA. Oral health of patients with cystic fi- brosis and their siblings[J]. J Dent Res, 1976,55 (6) :991 - 996.
  • 8Peker S, Mete S, Gokdemir Y, et al. Related factors of dental caries and molar incisor hypomineralisation in a group of children with cystic fibrosis [ J ]. Eur Arch Paediatr Dent, 2014,15 (4) : 275 - 280.
  • 9Ferrazzano GF, Orlando S, Sangianantoni G, et al. Dental and periodontal health status in children affected by cystic fibrosis in a southern Italian region [ J. Eur J Paediatr Dent, 2009, 10 (2) :65 -68.
  • 10Azevedo TD, Feijo GC, Bezerra AC. Presence of developmental defects of enamel in cystic fibrosis patients [ J 1. J Dent Child ( Chic), 2006,73 ( 3 ) : 159 - 163.

引证文献1

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