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Extraction and purification of TGFβ and its effect on the induction of apoptosis of hepatocytes 被引量:15
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作者 Xiao-Hui Si Lian-Jun Yang Research Institute of Stomatology,the Ninth People’s Hospital,Shanghai Second Medical University,Shanghai 200011,ChinaDepartment of Pathology,Fourth Military Medical University,Xi’an 710033,Shaanxi Province,China 《World Journal of Gastroenterology》 SCIE CAS CSCD 2001年第4期527-531,共5页
AIM To extract and purify the transforming growth factor β (TGF β), and to demonstrate its biological activity in vivo and induction of apoptosis of hepatocytes in vitro.METHODS TGF β was isolated from fresh bovine... AIM To extract and purify the transforming growth factor β (TGF β), and to demonstrate its biological activity in vivo and induction of apoptosis of hepatocytes in vitro.METHODS TGF β was isolated from fresh bovine platelets by acid/ethanol extraction method and purified with ion exchange and gel chromatography. The extracted TGF β was injected subcutaneously to mice, and its biological activity in vivo was observed 72 hfs post-injection by HE staining. The morphological changes were observed by HE staining and the occurrence of apoptosis was detected by TUNEL method after the human normal hepatic cell line QZG was treated with 8 μg@L 1 TGFβ for 12 hrs in vitro.RESULTS The molecular mass 25 ku TGF β protein was successfully extracted. It was able to induce localized granulation tissue formation in vivo. TGF β-treated hepatocytes showed obvious apoptotic morphological changes, including the pyknosis and dense-stained nuclei and cytoplasm, the fragmentary, annular or crescent nuclei, and the "bubbling" cytoplasm. Moreover, its apoptotic rate was significantly higher than that of the control group (P<0.05).CONCLUSION Biological active TGF β protein is extracted and purified successfully from bovine platelets, and it is able to induce the apoptosis of hepatocytes. 展开更多
关键词 transforming growth factor beta/isolation & purification transforming growth factor beta/pharmacology liver/cytology APOPTOSIS
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重组人TGF-β1融合蛋白的克隆、表达、纯化及鉴定 被引量:4
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作者 姜昌丽 张英起 颜真 《第四军医大学学报》 北大核心 2006年第3期193-195,共3页
目的构建人转化生长因子-β1(TGF-β1)基因的原核表达载体,表达并纯化GST-hTGFβ1.方法应用RT-PCR获得人TGF-β1的基因片段,成功构建人TGF-β1原核表达载体,诱导表达人TGF-β1与GST的融合蛋白;应用亲和层析法纯化重组融合蛋白,对纯化产... 目的构建人转化生长因子-β1(TGF-β1)基因的原核表达载体,表达并纯化GST-hTGFβ1.方法应用RT-PCR获得人TGF-β1的基因片段,成功构建人TGF-β1原核表达载体,诱导表达人TGF-β1与GST的融合蛋白;应用亲和层析法纯化重组融合蛋白,对纯化产物进行SDS-PAGE电泳分析和Western Blot检测分析.结果成功构建了人TGF-β1重组融合表达质粒pGEX-4T-1-TGF-β1,表达的蛋白经SDS-PAGE电泳分析,在Mr约为39×103处出现了一条新生的蛋白条带,该表达蛋白具有与TGF-β1抗体特异性的结合能力.结论成功构建了人TGF-β1基因的原核表达载体并纯化了该基因的原核表达产物,为下一步的人TGF-β1自体疫苗的研制奠定了基础. 展开更多
关键词 转化生长因子-Β1 重组融合蛋白/分离与纯化 pGEX4T-1载体
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截短型人转化生长因子βⅡ型受体胞外域的表达及活性分析
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作者 韩瑞杰 王小花 +3 位作者 左魁阳 初彦辉 李桂芹 刘海峰 《广东医学》 CAS 2018年第8期1124-1128,共5页
目的构建截短型人转化生长因子βⅡ型受体胞外域(thTβRⅡ)原核表达载体,诱导表达纯化thTβRⅡ蛋白,并分析其生物学活性。方法以本实验室前期构建的TβRⅡ全长基因片段(p GEX-4T1-TβRⅡ)为模版,常规PCR扩增出带有Nde I和Bam HI酶切位点... 目的构建截短型人转化生长因子βⅡ型受体胞外域(thTβRⅡ)原核表达载体,诱导表达纯化thTβRⅡ蛋白,并分析其生物学活性。方法以本实验室前期构建的TβRⅡ全长基因片段(p GEX-4T1-TβRⅡ)为模版,常规PCR扩增出带有Nde I和Bam HI酶切位点的thTβRⅡ目的基因,并插入原核表达载体p ET28a,命名为p ET28a-thTβRⅡ。将经过PCR、双酶切和DNA测序正确的p ET28a-thTβRⅡ转化至大肠杆菌Rossta诱导表达,用Ni^(2+)亲和层析纯化获得高纯度thTβRⅡ目的蛋白,经SDS-PAGE进行纯度分析,MTT法观察其对转化生长因子-β1(TGF-β1)活化的人肝星状细胞LX-2增殖活性的影响,real-time RT-PCR及Western blot检测其对TGF-β1、纤连蛋白(FN)mRNA及FN、α-平滑肌肌动蛋白(α-SMA)蛋白表达的影响。结果 p ET28a-thTβRⅡ原核表达载体构建成功,宿主菌Rossta/p ET28a-thTβRⅡ在37℃经0.8mmol/L异丙基-β-D-硫代半乳糖苷诱导5 h获得目的蛋白thTβRⅡ的大量表达,目的蛋白主要以包涵体的形式存在,通过Ni^(2+)亲和层析成功获得高纯度thTβRⅡ,SDS-PAGE鉴定分子量约为18.0 kD,MTT显示150μg/mL的重组蛋白thTβRⅡ能明显抑制活化的人肝星状细胞LX-2增殖,real-time RT-PCR及Western blot显示200μg/mL的重组蛋白thTβRⅡ其能显著减少TGFβ1、FNmRNA;FN、α-SMA蛋白的表达。结论成功构建thTβRⅡ原核表达载体,诱导表达纯化并获得高纯度重组蛋白thTβRⅡ,其能抑制活化的LX-2细胞增殖并具有抗纤维化作用,为进一步体内外功能研究打下基础。 展开更多
关键词 TGFβⅡ型受体 包涵体 纯化
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