安全与环境学报
安全與環境學報
안전여배경학보
JOURNAL OF SAFETY AND ENVIRONMENT
2010年
1期
1-7
,共7页
毒理学%差异蛋白质%大弹涂鱼%肝脏%镉%双向电泳%蛋白质组
毒理學%差異蛋白質%大彈塗魚%肝髒%鎘%雙嚮電泳%蛋白質組
독이학%차이단백질%대탄도어%간장%력%쌍향전영%단백질조
toxicology%differential proteins%Boleophthalmus pectinirostris%liver%cadmium%two-dimensional polyacrylamide gel electrophoresis (2-DE)%proteomics
采用双向电泳技术,对重金属镉暴露后海洋鱼类大弹涂鱼肝脏组织的差异蛋白质进行了研究.pH=5~8、7 cm胶条电泳图谱经PDquest软件分析,结果表明,对照组、慢性胁迫组和急性胁迫组平均检测到的蛋白点数分别为512±35、509±29和532±22,匹配率约为90%,急性镉胁迫后差异蛋白点数为14个,其中7个蛋白点在胁迫后表达量显著下调,4个蛋白点显著上调,消失1个蛋白点,并新增1个蛋白点.对其中7个差异蛋白点进行肽指纹图谱分析(MALDI-TOF-MS),差异蛋白分别为K18,prohibitin,GTP-binding protein Ypt1,two-component system response regulator,similar to T-complex protein 1 subunit theta (TCP-1-theta) (CCT-theta),transcriptional regulator,CopG family和mitogen-activated protein kinase homologue.而慢性镉胁迫后差异表达点数为15个,其中8个蛋白点在胁迫后表达量显著上升,5个蛋白点显著下调,消失1个蛋白点,并新增1个蛋白点.对其中6个差异蛋白点进行肽指纹图谱分析(MALDI-TOF-MS),差异蛋白分别为GTP-binding protein Ypt1,two-component system response regulator,hypothetical protein BT_1634,keratin 9,anscriptional regulator,CopG family和mitogen-activated protein kinase homologue.通过分析各蛋白的变化,探讨了慢性(0.05 mg/L,30 d)和急性(5 mg/L,3 d)重金属镉胁迫的致毒机制.在急慢性镉胁迫胁迫下,不仅大弹涂鱼体内的蛋白表达发生相应的变化,鱼体内环境的动态平衡也被打破.这种变化超过大弹涂鱼的自我解毒和保护能力,就会使得肝脏细胞的正常代谢受到破坏,引起细胞凋亡.
採用雙嚮電泳技術,對重金屬鎘暴露後海洋魚類大彈塗魚肝髒組織的差異蛋白質進行瞭研究.pH=5~8、7 cm膠條電泳圖譜經PDquest軟件分析,結果錶明,對照組、慢性脅迫組和急性脅迫組平均檢測到的蛋白點數分彆為512±35、509±29和532±22,匹配率約為90%,急性鎘脅迫後差異蛋白點數為14箇,其中7箇蛋白點在脅迫後錶達量顯著下調,4箇蛋白點顯著上調,消失1箇蛋白點,併新增1箇蛋白點.對其中7箇差異蛋白點進行肽指紋圖譜分析(MALDI-TOF-MS),差異蛋白分彆為K18,prohibitin,GTP-binding protein Ypt1,two-component system response regulator,similar to T-complex protein 1 subunit theta (TCP-1-theta) (CCT-theta),transcriptional regulator,CopG family和mitogen-activated protein kinase homologue.而慢性鎘脅迫後差異錶達點數為15箇,其中8箇蛋白點在脅迫後錶達量顯著上升,5箇蛋白點顯著下調,消失1箇蛋白點,併新增1箇蛋白點.對其中6箇差異蛋白點進行肽指紋圖譜分析(MALDI-TOF-MS),差異蛋白分彆為GTP-binding protein Ypt1,two-component system response regulator,hypothetical protein BT_1634,keratin 9,anscriptional regulator,CopG family和mitogen-activated protein kinase homologue.通過分析各蛋白的變化,探討瞭慢性(0.05 mg/L,30 d)和急性(5 mg/L,3 d)重金屬鎘脅迫的緻毒機製.在急慢性鎘脅迫脅迫下,不僅大彈塗魚體內的蛋白錶達髮生相應的變化,魚體內環境的動態平衡也被打破.這種變化超過大彈塗魚的自我解毒和保護能力,就會使得肝髒細胞的正常代謝受到破壞,引起細胞凋亡.
채용쌍향전영기술,대중금속력폭로후해양어류대탄도어간장조직적차이단백질진행료연구.pH=5~8、7 cm효조전영도보경PDquest연건분석,결과표명,대조조、만성협박조화급성협박조평균검측도적단백점수분별위512±35、509±29화532±22,필배솔약위90%,급성력협박후차이단백점수위14개,기중7개단백점재협박후표체량현저하조,4개단백점현저상조,소실1개단백점,병신증1개단백점.대기중7개차이단백점진행태지문도보분석(MALDI-TOF-MS),차이단백분별위K18,prohibitin,GTP-binding protein Ypt1,two-component system response regulator,similar to T-complex protein 1 subunit theta (TCP-1-theta) (CCT-theta),transcriptional regulator,CopG family화mitogen-activated protein kinase homologue.이만성력협박후차이표체점수위15개,기중8개단백점재협박후표체량현저상승,5개단백점현저하조,소실1개단백점,병신증1개단백점.대기중6개차이단백점진행태지문도보분석(MALDI-TOF-MS),차이단백분별위GTP-binding protein Ypt1,two-component system response regulator,hypothetical protein BT_1634,keratin 9,anscriptional regulator,CopG family화mitogen-activated protein kinase homologue.통과분석각단백적변화,탐토료만성(0.05 mg/L,30 d)화급성(5 mg/L,3 d)중금속력협박적치독궤제.재급만성력협박협박하,불부대탄도어체내적단백표체발생상응적변화,어체내배경적동태평형야피타파.저충변화초과대탄도어적자아해독화보호능력,취회사득간장세포적정상대사수도파배,인기세포조망.
The aim of the present study is to characterize differental protein exposure profiles in the liver of Boleophthalmus pectinirostris after cadmium (Cd) exposure through the proteomic approaches. For this purpose, we have developed a two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) technique for examining the response of the proteome from the liver tissue of Boleophthalmus pectinirostris to test its extremely severe cadmium toxicity. Actually, about 530 protein spots have been detected from the liver samples to a 2D-PAGE gel in the pH range 5-8. Fish of this sort exposed were supposed to be separated into three groups: an acute exposure group (5 mg/L for 3 days), a chronical exposure (0.05 mg/L for 30 days), and a control group (no Cd). The results of our examination show that the total amount of proteins found in the control group, the acute exposure group and chronical exposure group were 512±35, 509±29 and 532±22, respectively. The matching rate in average was 90%. For more specific purposes, 14 protein spots were found differentially exposed after the acute Cd exposure by two-dimensional gel electrophoresis (2-DE). The exposure of the 8 proteins among them were significantly down-regulated, with four of them being up-regulated, one merely seen in the control, and the one added. Seven of them were thern analyzed by using MALDI-TOF-MS. The results of our examination demonstrates that the proteins were K18, prohibitin, GTP-binding protein Ypt1, two-componential system response regulator, similar to T-complex protein 1 subunit theta (TCP-1-theta) (CCT-theta), transcriptional regulator, CopG family and mitogen-activated protein kinase homologue, respectively. The fifteen protein spots were found differentially exposed after the chronic Cd exposure, whereas eight spots among them were found significantly up-regulated,and five down-regulated, with one only noticed in control, and one added. In addition, 6 of them were analyzed by using MALDI-TOF-MS. The results of our examination suggest that the 6 proteins were GTP-binding protein Ypt1, the two-componential system response regulator, hypothetical protein BT_1634, keratin 9, and inscriptional regulator CopG family and mitogen-activated protein kinase homologue, respectively. Based on their variable levels and trends on the 2D-PAGE gel, this protein exposure examination suggestes that the finding can be utilized as biomarkers to investigate cadmium pollution degrees in the halobios survival, and evaluate the degree of risk of the human fatalities. In addition, the result of this research reveal that the element cadmium can not only result in differences in protein exposure profiles of Boleophthalmus pectinirostris, but also could induce the homeostasis, even further leading to the apoptosis.