{"title":"安德氏隐孢子虫atp结合盒1基因的克隆与离子转运","authors":"Ju-hua Wang, Pan Wang, Chuan-huan Liu, Xiu-mei Sun, Qian-qian Xie, Xiu-heng Xue","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the transportation of intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) under the function of Cryptosporidium andersoni ATP-binding cassette (CaABC) 1 gene.</p><p><strong>Methods: </strong>CaABC1 gene was amplified by PCR using specifically designed primers. The eukaryotic expression plasmid pEGFP-C1-CaABC1 was constructed, and transfected into mouse intestinal epithelial cells via liposome transfection. The blank (with no transfection) and control groups (transfected with empty plasmid pEGFP-C1) were also set. Changes in intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) concentrations were examined by the ion concentration assay kit.</p><p><strong>Results: </strong>PCR amplification resulted in a 544 bp product. The recombinant plasmid pEGFP-C1-CaABC1 was successfully constructed. Green fluorescence was seen in the control and transfected groups, but not in the blank group. The concentrations of K(+), Ca(2+), Na(+) and Mg(2+) in intracellular fluid were (5.51 ± 0.51), (1.98 ± 0.06), (108.33 ± 1.33) and (0.93 ± 0.03) mmol/L in the blank group; (6.25 ± 0.70), (1.90 ± 0.13), (107.73 ± 1.79) and (0.87 ± 0.05) mmol/L in the control group; and (14.84 ± 0.90), (3.40 ± 0.14), (127.64 ± 1.49) and (1.72 ± 0.20) mmol/L in the transfected group. The concentrations of K+, Ca2+, Na+ and Mg2+ in extracellular fluid were (12.72 ± 0.83), (3.72 ± 0.03), (116.83 ± 1.04) and (2.02 ± 0.18) mmol/L in the blank group; (10.11 ± 0.90), (3.58 ± 0.06), (115.89 ± 1.86) and (1.71 ± 0.41) mmol/L in the control group; and (5.77 ± 0.21), (1.29 ± 0.18), (96.21 ± 1.19) and (0.64 ± 0.02) mmol/L in the transfected group. There were significant differences in K+, Ca2+ and Mg2+ concentrations between the transfected group and the control group.</p><p><strong>Conclusion: </strong>CaABC1 participates in the transportation of K+, Ca2+ and Mg2+.</p>","PeriodicalId":23981,"journal":{"name":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","volume":"34 4","pages":"326-30"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Cloning and Ion Transportation of Cryptosporidium andersoni ATP-binding Cassette 1 Gene].\",\"authors\":\"Ju-hua Wang, Pan Wang, Chuan-huan Liu, Xiu-mei Sun, Qian-qian Xie, Xiu-heng Xue\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the transportation of intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) under the function of Cryptosporidium andersoni ATP-binding cassette (CaABC) 1 gene.</p><p><strong>Methods: </strong>CaABC1 gene was amplified by PCR using specifically designed primers. The eukaryotic expression plasmid pEGFP-C1-CaABC1 was constructed, and transfected into mouse intestinal epithelial cells via liposome transfection. The blank (with no transfection) and control groups (transfected with empty plasmid pEGFP-C1) were also set. Changes in intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) concentrations were examined by the ion concentration assay kit.</p><p><strong>Results: </strong>PCR amplification resulted in a 544 bp product. The recombinant plasmid pEGFP-C1-CaABC1 was successfully constructed. Green fluorescence was seen in the control and transfected groups, but not in the blank group. The concentrations of K(+), Ca(2+), Na(+) and Mg(2+) in intracellular fluid were (5.51 ± 0.51), (1.98 ± 0.06), (108.33 ± 1.33) and (0.93 ± 0.03) mmol/L in the blank group; (6.25 ± 0.70), (1.90 ± 0.13), (107.73 ± 1.79) and (0.87 ± 0.05) mmol/L in the control group; and (14.84 ± 0.90), (3.40 ± 0.14), (127.64 ± 1.49) and (1.72 ± 0.20) mmol/L in the transfected group. The concentrations of K+, Ca2+, Na+ and Mg2+ in extracellular fluid were (12.72 ± 0.83), (3.72 ± 0.03), (116.83 ± 1.04) and (2.02 ± 0.18) mmol/L in the blank group; (10.11 ± 0.90), (3.58 ± 0.06), (115.89 ± 1.86) and (1.71 ± 0.41) mmol/L in the control group; and (5.77 ± 0.21), (1.29 ± 0.18), (96.21 ± 1.19) and (0.64 ± 0.02) mmol/L in the transfected group. There were significant differences in K+, Ca2+ and Mg2+ concentrations between the transfected group and the control group.</p><p><strong>Conclusion: </strong>CaABC1 participates in the transportation of K+, Ca2+ and Mg2+.</p>\",\"PeriodicalId\":23981,\"journal\":{\"name\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"volume\":\"34 4\",\"pages\":\"326-30\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Cloning and Ion Transportation of Cryptosporidium andersoni ATP-binding Cassette 1 Gene].
Objective: To investigate the transportation of intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) under the function of Cryptosporidium andersoni ATP-binding cassette (CaABC) 1 gene.
Methods: CaABC1 gene was amplified by PCR using specifically designed primers. The eukaryotic expression plasmid pEGFP-C1-CaABC1 was constructed, and transfected into mouse intestinal epithelial cells via liposome transfection. The blank (with no transfection) and control groups (transfected with empty plasmid pEGFP-C1) were also set. Changes in intracellular and extracellular K(+), Ca(2+), Na(+) and Mg(2+) concentrations were examined by the ion concentration assay kit.
Results: PCR amplification resulted in a 544 bp product. The recombinant plasmid pEGFP-C1-CaABC1 was successfully constructed. Green fluorescence was seen in the control and transfected groups, but not in the blank group. The concentrations of K(+), Ca(2+), Na(+) and Mg(2+) in intracellular fluid were (5.51 ± 0.51), (1.98 ± 0.06), (108.33 ± 1.33) and (0.93 ± 0.03) mmol/L in the blank group; (6.25 ± 0.70), (1.90 ± 0.13), (107.73 ± 1.79) and (0.87 ± 0.05) mmol/L in the control group; and (14.84 ± 0.90), (3.40 ± 0.14), (127.64 ± 1.49) and (1.72 ± 0.20) mmol/L in the transfected group. The concentrations of K+, Ca2+, Na+ and Mg2+ in extracellular fluid were (12.72 ± 0.83), (3.72 ± 0.03), (116.83 ± 1.04) and (2.02 ± 0.18) mmol/L in the blank group; (10.11 ± 0.90), (3.58 ± 0.06), (115.89 ± 1.86) and (1.71 ± 0.41) mmol/L in the control group; and (5.77 ± 0.21), (1.29 ± 0.18), (96.21 ± 1.19) and (0.64 ± 0.02) mmol/L in the transfected group. There were significant differences in K+, Ca2+ and Mg2+ concentrations between the transfected group and the control group.
Conclusion: CaABC1 participates in the transportation of K+, Ca2+ and Mg2+.