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SSB1在腮腺放射性损伤修复过程中的表达变化 被引量:2

The expression of SSB1 in radioactive damage repair of parotid gland
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摘要 目的:研究正常大鼠腮腺及放射后大鼠腮腺组织单链DNA结合蛋白(single-strand DNA-binding protein1,SSB1)的表达及变化规律,探讨SSB1与涎腺放射损伤修复的关系。方法:取近交系成年Wistar大鼠40只,一次给予6 Gy剂量照射头颈部,于放射后每小时随机处死5只动物取腮腺组织,共形成8个实验组,另取5只大鼠作为对照组。应用免疫组织化学与RT-qPCR的方法检测SSB1在大鼠腮腺组织中表达情况。结果:对照组大鼠腮腺组织有一定量的内源性SSB1表达,不同腮腺组织之间SSB1含量不同,导管>腺泡>结缔组织;放射后,大鼠腮腺组织中SSB1的表达量随着时间变化呈先增加(P<0.05)后减弱趋势,并在后期表达量降至接近正常水平。结论:辐射能诱导大鼠腮腺SSB1表达量增加,可能参与了大鼠腮腺放射性损伤修复过程。 Objective: To investigate the expression of single-strand DNA-binding protein 1( SSB1) in rats' normal and irradiated parotid gland tissue,and explore the relationship between SSB1 and radioactive damage repair. Methods: Take the normal rats as control( n = 5),the experimental rats( n = 40) were radiated with 60 Co gamma rays on head and neck region in a dose of 6 Gy. Five rats were randomly killed per hour to form eight experimental groups after irradiation. Immunohistochemical and RT-qPCR were applicated to detect the expression of SSB1 in rats parotid gland. Results: A certain amount of endogenous SSB1 was expressed in normal rats parotid gland tissue. The content of SSB1 was different in different parotid gland tissues,ducts acinus connective tissue. SSB1 was displayed a increasing first( P 0. 05) and after weakening trend over time after irradiation and the unper expression was close to nomal. Conclusion: SSB1 is a radiation-induced protein,which may be involved in radioactive damage repair process in the rats' parotid gland.
作者 曾祥林 王代友 蓝铁瓒 曹阳 于萧 ZENG Xiang-lin WANG Dai-you JAN Tie-zan CAO Yang YU Xiao.(Department of Oral and Maxillofacial Surgery, Collage of Stomatology, Guangxi Medical Univer- sity, Guangxi Nanning .530021, China)
出处 《临床口腔医学杂志》 2016年第9期527-530,共4页 Journal of Clinical Stomatology
基金 广西重点自然科学基金(2014GXNSFDA118022)
关键词 单链DNA结合蛋白 腮腺 放射性损伤 DSBs修复 Single-strand DNA-binding protein 1 Parotid gland Radioactive damage DSBs repair
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  • 1王代友,于大海,温玉明,巫家晓,韦山良.大鼠软组织血管放射损伤动物模型的建立[J].中华放射医学与防护杂志,2004,24(4):302-303. 被引量:5
  • 2Richard DJ, Bolderson E, Khanna KK. Multiple human single-stranded DNA binding proteins function in genome maintenance: structural, biochemical and functional analysis. Crit Rev Biochern Mol Bioi 2009; 44:98-116.
  • 3Flynn RL, Zou L. Oligonucleotide/oligosaccharide-binding fold proteins: a growing family of genome guardians. Crit Rev Biochem Mol Biol 2010; 45:266-275.
  • 4Limbo 0, Chahwan C, Yamada Y, de Bruin RA, Wittenberg C, Russell P. Ctpl is a cell-cycle-regulated protein that functions with Mre11 complex to control double-strand break repair by homologous recombination. Mol Cell 2007; 28:134-146.
  • 5Sartori AA, Lukas C, Jackson SP, et al. Human CtIP promotes DNA end resection. Nature 2007; 450:509-514.
  • 6Bartek J, Lukas J. DNA repair: Damage alert. Nature 2003; 421:486-488.
  • 7Zou L, Elledge SJ. Sensing DNA damage through ATRlP recognition ofRPA-ssDNA complexes. Science 2003; 300:1542- 1548.
  • 8Moynahan ME, Jasin M. Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis. Nat Rev Mol Cell Biol 2010; 11:196-207.
  • 9Griffith JD, Comeau L, Rosenfield S, et al. Mammalian telomeres end in a large duplex loop. Cell 1999; 97:503-514.
  • 10Murti KG, Prescott DM. Telomeres of polytene chromosomes in a ciliated protozoan terminate in duplex DNA loops. Proc Natl Acad Sci USA 1999; 96:14436-14439.

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