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1.
本试验以水牛卵母细胞为研究对象,通过基于双向电泳-质谱技术的蛋白质组学研究手段,鉴定卵母细胞成熟前后表达量存在变化的蛋白质并进行验证。通过优化方法建立水牛卵母细胞蛋白质双向电泳分离的技术体系,通过双向电泳(2-DE)获得成熟前后的卵母细胞蛋白质电泳图谱,软件分析得到差异表达蛋白质,对差异蛋白质进行飞行时间质谱(MALDI-TOF/TOF)分析,部分差异蛋白质合成抗体进行Western blot验证。结果表明,2组卵母细胞样品均获得约300个蛋白质斑点的双向电泳图谱。经ImageMaster软件比对分析,共发现在水牛卵母细胞成熟前后有27个差异蛋白质,其中表达上调15个,表达下调12个。将差异蛋白质斑点胶内酶解后用于MALDITOF/TOF飞行时间质谱鉴定,成功鉴定了6个蛋白质,包括主要穹窿蛋白(MVP)、热激蛋白60(HSP60)、Ras应答结合原件蛋白1(RREB1)等。Western blot结果表明,HSP60蛋白表达与双向电泳结果一致。本试验发现一批在卵母细胞成熟前后的差异表达蛋白质并进行表达量验证,推测HSP60蛋白可能在体外成熟时起到保护卵母细胞和物质转运的作用。  相似文献   

2.
本试验旨在比较分析雏鸡冷应激前后血清中蛋白质的表达差异,并对重点差异蛋白质进行鉴定。将30只雏鸡随机分为3组,分别为冷应激组、冷适应组和常温对照组,收集各组雏鸡的血液制备血清后进行双向凝胶电泳(2-DE),以获得血清蛋白质表达的2-DE图谱,对2-DE图谱进行差异分析(利用PDQuest 8.0软件),随后采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)技术对差异表达蛋白质进行鉴定,并利用蛋白质印迹(Western blot)方法进行验证。结果显示:通过2-DE对常温对照组、冷应激组和冷适应组雏鸡血清进行分析,得到了比较完整的差异蛋白质数据,共找到差异蛋白质点23个。采用MALDI-TOF-MS技术分析其中几个重复性好且较为明显的蛋白质点,成功鉴定出4个差异蛋白质,其中2个为果糖二磷酸醛缩酶C(ALDOC),是参与葡萄糖、能量代谢通路供能的相关蛋白;随后,对差异蛋白质ALDOC进行Western blot验证,所得结果与2-DE的结果相一致。结果表明,雏鸡冷应激前后血清中蛋白质的表达具有明显的差异,这些蛋白质的表达差异可能与冷应激有关。  相似文献   

3.
本研究以奶牛乳腺组织为对象,采用了普通离心、超速离心、2-D clean-up kit和TCA/丙酮沉淀方法制备蛋白质样品,经二维凝胶电泳(2-DE)获得蛋白表达图谱。根据凝胶图谱上蛋白质斑点判断图谱的质量,并运用PDQuest7.4软件分析图谱。结果显示:普通离心法制备的蛋白样品的凝胶图谱蛋白质斑点较为清晰,但横向条纹较多;超速离心法纯化蛋白样品的图谱,蛋白斑点清晰且可检测到较多的斑点;TCA/丙酮沉淀和2-D clean-up kit方法纯化蛋白样品的凝胶图谱条纹减少,蛋白斑点清晰,但可检测到的斑点数量有所减少。研究表明,超速离心方法纯化的蛋白质样品适合建立奶牛乳腺组织的蛋白质表达图谱。  相似文献   

4.
雏鸡法氏囊蛋白质组学双向电泳技术的建立及其初步分析   总被引:2,自引:2,他引:0  
为了建立并优化鸡法氏囊蛋白质组学的双向电泳技术体系,以不同日龄雏鸡的法氏囊组织为研究对象,用固相pH梯度胶条进行等电聚焦、SDS-PAGE垂直电泳,采用不同的样品制备方法,对上样量、水化、等电聚焦、胶条平衡和凝胶染色方法等进行一系列优化,并应用PDQuest8.0.1软件对图谱进行初步分析.结果显示法氏囊组织在pH 5~8范围、17 cm的2-DE胶上可以得到很好的分离,胶体考染后经PDQuest软件分析,在正常法氏囊组织可检测到800个以上蛋白点,不同2-DE图谱间蛋白点平均匹配率为83.5%,不同日龄雏鸡法氏囊存在有明显表达差异的蛋白质点37个,其中表达上调蛋白点17个,表达下调蛋白点11个,新增蛋白点5个,消失蛋白点4个,试验建立的鸡法氏囊组织蛋白质组双向电泳技术为法氏囊发育进化及其免疫功能的研究提供了新技术和方法.  相似文献   

5.
Asia1型FMDV感染BHK-21细胞差异蛋白质点2-DE分析   总被引:1,自引:0,他引:1  
为研究Asia 1型口蹄疫病毒(FMDV)感染BHK-21细胞后蛋白质组的变化及差异,将FMDV接种于培养的单层BHK-21细胞,同时设未接毒的BHK-21细胞作对照组.待细胞病变后分别提取2组细胞总蛋白借助2-DE技术及PDQuest8.0软件进行细胞蛋白质组二维电泳图谱差异性分析.结果显示感染组有1 457个可见蛋白质点,而对照组可见的蛋白质点为1 427个.感染组蛋白点的表达量与对照组相比,二者具有统计学差异(P<0.05)的蛋白质点472个,其中表达上调251个点,表达下调221个点,新合成蛋白点30个.结果表明FMDV感染BHK-21细胞后弓l起了细胞蛋白质组表达模式的改变,这种变化是病毒与细胞相互作用的结果.本研究首次利用蛋白质组学技术研究Asia 1型FMDV感染BHK-21细胞后蛋白质组学差异,有助于深入研究Asia 1型FMDV和BHK-21细胞相互作用的分子机制.  相似文献   

6.
亚细胞蛋白质组的优点在于对低丰度蛋白的研究,运用亚细胞蛋白质组学的研究策略,可以提高低丰度蛋白质在双向电泳中的检出数量.通过分析奶牛乳腺炎乳腺与正常乳腺核蛋白组差异表达情况,为奶牛乳腺炎发病机理研究寻找尽可能多的生物标记分子.经超速离心法分离细胞核,双向凝胶电泳分离蛋白,用PDQuest7.4软件分析寻找差异蛋白质斑点,高效液相色谱串联离子阱质谱鉴定蛋白质.从核蛋白组2-DE图谱中筛选出22个差异表达的蛋白质斑点,质谱鉴定出17个差异表达的蛋白质,2个蛋白质在乳腺炎发病过程中下调,7个上调,5个只在正常情况下表达,3个只表达在乳腺炎组织中,筛选出的差异表达蛋白质涉及细胞骨架构成、代谢调节及凋亡调控等许多方面.表明奶牛乳腺炎发生时乳腺组织核结构和代谢状态都发生了的变化.  相似文献   

7.
运用亚细胞蛋白质组学的研究策略,分离纯化亚细胞结构再进行蛋白质组学研究,可提高低丰度蛋白在双向凝胶电泳中的检出率。通过对比分析乳腺炎奶牛乳腺与正常奶牛乳腺线粒体蛋白质组的表达变化,为奶牛乳腺炎的生物学治疗及抗病育种工作筛选出目基因和蛋白。超速离心法分离线粒体,双向凝胶电泳分离蛋白,PDQuest7.4软件分析差异蛋白斑点,高效液相色谱串联离子阱质谱鉴定差异蛋白。从奶牛乳腺线粒体蛋白2-DE图谱中筛选出17个差异表达的蛋白质斑点,质谱鉴定出17个差异表达蛋白(6个蛋白在奶牛乳腺炎发生过程中下调,8个上调,1个只在正常情况下表达,2个只在乳腺炎乳腺组织中表达)。筛选出的差异蛋白质涉及到细胞的能量代谢、蛋白质合成、mRNA的加工成熟及调亡调控等许多方面,表明奶牛乳腺炎发生时乳腺线粒体组织结构和代谢状态都发生了明显的变化。  相似文献   

8.
郭宪  裴杰  褚敏  王宏博  丁学智  阎萍 《中国畜牧兽医》2015,42(11):3037-3043
从蛋白质水平了解牦牛季节性繁殖规律,利用双向电泳与质谱鉴定技术分析牦牛卵泡液与血浆蛋白质组分变化。以青海高原牦牛卵泡液与血浆为研究对象,采用双向电泳技术构建牦牛卵泡液与血浆蛋白质双向电泳图谱,银染后利用Image Master 2D Platinum软件分析并采用MALDI-TOF-MS进行质谱鉴定。用试剂盒ProteoExtract Albumin/IgG Removal Kit去除高丰度蛋白质后,利用2-DE技术获得了分辨率较高的卵泡液与血浆蛋白质电泳图谱,卵泡液与血浆蛋白质图谱对比分析共发现了24个差异表达蛋白质点,其中2个蛋白质点表达上调,22个蛋白质点表达下调。经质谱分析,最终成功鉴定出8个蛋白质点、5个未知蛋白质点。本研究成功构建了蛋白质图谱及分离鉴定的差异蛋白质,为从蛋白质水平揭示牦牛卵泡发育规律及了解卵母细胞发育的微环境提供了试验依据。  相似文献   

9.
利用双向电泳技术可以对体外培养的2型猪链球菌强毒株和无毒株进行胞外蛋白质组比较,寻找与毒力相关的蛋白质.2型猪链球菌强毒株和无毒株在无蛋白细菌培养液中37℃摇床培养16 h,从培养物上清中获得胞外蛋白.第一向电泳用pH4-7线性IPG胶条进行等电聚焦,第二向电泳用SDS-PAGE凝胶再分离蛋白,经过考马斯亮蓝R350染色,图像扫描后,利用软件分析处理图像.在2型猪链球菌强毒株和无毒株的胞外蛋白质图谱中都分别检测出180±10个蛋白质斑点,它们的蛋白质分子质量分布基本相似;在所检测到的差异蛋白质斑点中,其中有50个蛋白斑点只存在于无毒株中而强毒株中不存在,有52个蛋白斑点只存在于强毒株中而无毒株中不存在,有7个蛋白斑点的表达量相差达5倍以上.这为研究2型猪链球菌的致病机理提供了蛋白质组学方面的信息.  相似文献   

10.
应用差异蛋白质组学研究感染新型鸭呼肠孤病毒(NDRV)番鸭后的肝和正常番鸭肝的蛋白质组差异,为深入研究NDRV的致病机制奠定良好理论基础。通过二维双向凝胶电泳技术和MALDI-TOF-TOF质谱仪分析获取NDRV感染组与非感染对照组之间的差异表达蛋白质,并运用蛋白质搜索鉴定软件Mascot 2.3.02鉴定蛋白质。结果共鉴定出26个差异表达蛋白质。感染组和非感染对照组比较,感染组肝中有9个表达下调的蛋白质和12个表达上调的蛋白质,3个表达蛋白质仅出现在非感染组,2个表达蛋白质仅出现在感染组。NDRV感染组的番鸭肝有肝细胞受损现象。差异蛋白质组学为NDRV分子发病机制的分析提供了一个新途径。  相似文献   

11.
旨在探索高铜对大鼠肝组织损伤的作用机制。试验选取120只SD大鼠随机分为对照组、高铜I组、高铜II组、高铜III组和高铜IV组,分别连续每天按体重灌胃0、20、40、80、160 mg·kg-1铜63 d,采集肝组织。使用ICP-MS测定肝组织铜含量,病理切片观察肝组织病理变化,透射电镜观察线粒体形态和线粒体自噬小体,RT-qPCR和Western blot检测肝组织NLRP3、Caspase-1、GSDMD、IL-1β、IL-18、Pink1、Parkin、LCB3、p62的mRNA和蛋白表达水平。结果显示,随着灌胃铜水平的增加,蓄积在肝组织中的铜含量呈剂量依赖性增加,且长期高水平铜暴露会造成明显的肝组织结构破坏;随着铜暴露水平的增加,线粒体自噬和细胞焦亡水平呈先上升后下降趋势;与对照组相比,高铜Ⅱ组、Ⅲ组中PINK1和LC3II/LC3I的mRNA和蛋白表达水平显著上升(P<0.05),高铜Ⅱ组中p62的mRNA和蛋白表达水平显著降低(P<0.05),高铜Ⅲ组NLRP3、Caspase-1、GSDMD、IL-1β的mRNA和蛋白表达水平显著上升(P<0.05),高铜IV组表现为下调。高铜长期暴露可通过影响线粒体自噬和细胞焦亡诱导大鼠肝组织损伤。  相似文献   

12.
试验的目的是考查以硫酸铜、碱式氯化铜、蛋氨酸铜、纳米铜和纳米小肽螯合铜等不同铜源供给形式对小白鼠铜排泄和血液免疫指标的影响。试验将120只18日龄小白鼠随机分为Ⅰ(小肽+硫酸铜组)、Ⅱ(硫酸铜组)、Ⅲ(碱式氯化铜组)、Ⅳ(蛋氨酸铜组)、Ⅴ(纳米铜组)和Ⅵ(纳米小肽螯合铜)等6个处理组,每个处理组设4个重复,每个重复5只小白鼠。饲喂试验分0~56、~121、3~192、0~26和27~33 d 5个阶段。其中0~5 d为预饲期,后4个阶段为试验期。预饲期和试验期各处理组采用相同的基础日粮。试验期Ⅰ~Ⅵ组饲粮铜的含量(以铜计)在6~12、13~19、20~26和27~33 d 4个阶段分别为2.5、5、10及15 mg/kg。结果表明,纳米小肽螯合铜组小鼠的铜排泄量显著低于其它各组。饲喂第2、3、4阶段,纳米小肽螯合铜组小鼠的血清免疫蛋白IgGI、gMI、gA、胰岛素样生长因子-1(IGF-1)及白介素-2(IL-2)均极显著(P<0.01)高于其它各组。  相似文献   

13.
试验旨在观察蟾酥微丸对小鼠急性毒性和大鼠长期毒性作用,评价其安全性,为临床用药提供理论依据。急性毒性试验选取昆明小鼠,2次灌服蟾酥微丸,测定蟾酥微丸的急性毒性。亚慢性毒性试验选取120只SD大鼠,平均分为低、中、高蟾酥微丸药物组和空白组(给予等体积的蒸馏水),灌胃给药,分别在连续给药28 d后和停药2周后称重,随机选取每组20只大鼠(停药后余下10只)心脏采血处死,检测血液学、血液生化指标并做病理组织学检查。急性毒性试验用药死亡时间集中在1~4 h,经计算LD50为13.21 g/kg。亚慢性毒性试验中,连续给药28 d后,高、中剂量组雄性大鼠的体重与空白组差异极显著(P<0.01);高剂量组的谷草转氨酶与碱性磷酸酶与空白组相比差异极显著(P<0.01);高、中剂量组的肾脏系数与空白组相比差异极显著(P<0.01)。经过2周停药恢复,高剂量组的生化指标恢复不佳,而中、低剂量组则恢复良好。病理学检查结果表明,高、中剂量组大鼠的肝脏、肾脏出现肿胀淤血,高剂量大鼠的肝脏表面有水泡样病灶。结果表明,蟾酥微丸的急性毒性较小,安全性较高;大剂量长期使用可导致肝脏、肾脏损伤,故临床应用要注意剂量和疗程。  相似文献   

14.
The aim of the experiment was to observe the acute toxicity and the long-term toxicity of Chansu pellets in mice, and to evaluate its safety and provide the theoretical basis for clinical use. Kunming mice were selected for acute toxicity test. The acute toxicity of Chansu pellets was determined by oral administration to mice twice. In the sub-chronic toxicity test, 120 SD rats were divided into low, middle and high dose groups and the control group (the same volume of distilled water) intragastric administration. Respectively, after 28 d of continuous administration and 2 weeks after drug withdrawal, the rats were weighed, and 20 rats (10 mice remaining after cessation of administration) in each group were sacrificed at random. The hematological and biochemical parameters were measured and the histopathological examination was performed. In the acute toxicity, time of death concentrated in 1 to 4 h. LD50 was 13.21 g/kg. In the sub-chronic, after 28 d of continuous dosing, the body weights of male rats of high dose group and the control group were extremely significantly different (P <0.01). Aspartate aminotransferase and alkaline phosphatase of high dose group were extremely significantly different (P <0.01) compared with control group. Kidneys coefficients of high and middle dose groups compared with control group were extremely significantly different (P <0.01). After two weeks the withdrawal recovery, biochemical indicators of high dose group's recovery was not good. Middle and low dose groups had good recovery. Pathological examination showed that high and middle dose groups' rat liver and kidney swelling congestion. High dose rat liver surface were blister-like lesions. The results showed that Chansu pellets were less acute toxicity. Long-term use of large doses could cause liver and kidney damage. Therefore, we should pay attention to dose and duration of treatment in clinical application.  相似文献   

15.
The amounts of DNA single strand breaks that are oxidative damage produced by copper were examined by comet assay in the liver cells of an inbred strain of Long-Evans Cinnamon (LEC) rats that spontaneously develops fulminant hepatitis. At 4 weeks of age, copper contents in the liver of LEC rats were approximately 30-fold higher than those of WKAH rats that are control rats used in the present study. Copper accumulated in the liver of LEC rats in an age-dependent manner and no significant differences were observed between copper contents in the livers of males and females at each week of age from 4 to 15 weeks. No significant amounts of DNA strand breaks were found in the liver cells of both male and female WKAH rats from 4 to 15 weeks of age. DNA strand breaks were produced in the substantial population of LEC rat liver cells at 10 weeks of age and induced in an age-dependent manner from 10 to 15 weeks of age. The amounts of DNA strand breaks produced by copper accumulation in the liver cells of female LEC rats are not more abundant than those in the cells of male rats, although it has been reported that hepatitis in female rats is more serious than that in male rats.  相似文献   

16.
In order to evaluate the toxicity of Wu Jin granules for the guidance of clinical treatment, the acute and sub-chronic toxicity were assessed in KM mice and Wistar rats, respectively.The results of acute toxicity test suggested that the LD50 of Wu Jin granules was >40 g/(kg·BW), maximal tolerance dose was 160 g/(kg·BW), equivalent to 80 times of clinical dosage.In sub-chronic toxicity test, the growth and general behavior of the animals appeared normal.Compared with the control group, weight gain and feed consumption of Wistar rats in the treatment groups had no significant difference (P>0.05).In high dose group, serum bilirubin (T-BIL), total protein (TP), albumin (ALB), urea nitrogen (BUN) and creatinine (CREA) of female Wistar rats, whereas CREA levels and liver index of male Wistar rats were significant difference (P<0.05), and the differences in other indexes were not significant (P>0.05); Hematological indexes, biochemical indexes of blood and organ index of Wistar rats in low dose group and medium dose group were not significantly different compared to the control group (P>0.05).Pathological examination results showed that mild granular degeneration existed in liver of Wistar rats in high dose group, whereas appeared clear and normal organizational structure of liver in Wistar rats in other groups.Wu Jin granules could inhibit intake of free bilirubin and hepatic synthesis protein in high dosage, whereas this results were not observed in other groups.Thus, the Wu Jin granules were safe in clinical treatment.  相似文献   

17.
本研究旨在评价乌锦颗粒剂的毒性,为临床安全用药提供理论依据。试验分别以昆明小鼠和Wistar大鼠为研究对象,进行急性毒性试验和亚慢性毒性试验研究。急性毒性试验结果显示,乌锦颗粒剂的半数致死量(LD50)>40 g/kg体重,最大给药量为160 g/kg体重,相当于临床用药量的80倍;在亚慢性毒性试验中,动物一般情况正常,试验组Wistar大鼠增重和饲料消耗量与对照组相比无显著差异(P>0.05);与对照组相比,高剂量组中雌鼠血清胆红素(T-BIL)、总蛋白(TP)、白蛋白(ALB)、尿素氮(BUN)和肌酐(CREA)及雄鼠CREA和肝脏指数均有显著差异(P<0.05),而其他指标与对照组相比差异均不显著(P>0.05);低剂量组和中剂量组Wistar大鼠血常规、血液生化指标和脏器指数与对照组相比差异均不显著(P>0.05);病理学检查发现高剂量组Wistar大鼠肝脏出现轻微颗粒变性,其他组Wistar大鼠组织结构清晰正常。结果表明,高剂量的乌锦颗粒剂能抑制肝脏对游离胆红素的摄入及蛋白质的合成;低剂量和中剂量乌锦颗粒剂此作用不明显。综合分析,乌锦颗粒剂临床用药是安全的。  相似文献   

18.
本研究旨在探究恩诺沙星与磺胺二甲嘧啶的联合毒性。选取SD大鼠为试验对象,将其分成6组,每组12只,分别为高剂量联合用药组(500 mg/kg体重)、中剂量联合用药组(250 mg/kg体重)、低剂量联合用药组(50 mg/kg体重)、恩诺沙星单药组(250 mg/kg体重)、磺胺二甲嘧啶单药组(250 mg/kg体重)及对照组(等量0.5%羧甲基纤维素钠溶液),配制相应的药物进行灌胃,最后一次给药1 d后对大鼠进行称重、麻醉、心脏采血并剖检取肝脏组织,然后对大鼠增重率、血常规指标、血清生化指标及肝脏病理学变化几个方面进行分析,并利用SPSS 22.0软件评估2种药物的联合作用效果。结果显示,在雌性大鼠中,高、中剂量联合用药组使大鼠增重率显著下降(P<0.05),雄性大鼠增重率无显著变化(P>0.05);雄性大鼠给药组白细胞数量均显著增加(P<0.05),高剂量联合用药组中性粒细胞和淋巴细胞占比分别表现为显著升高及下降(P<0.05);高、中剂量联合用药组大鼠外周血中谷草转氨酶含量显著增加(P<0.05),且高、中剂量联合用药组肝脏病理切片视野可见不同程度的炎性细胞浸润,并伴有不同程度的损伤。本研究结果表明,恩诺沙星和磺胺二甲嘧啶联用可使毒性增加,对大鼠的免疫系统状态有一定的影响,且能造成一定程度的肝脏损伤,剂量越高影响越大。本研究为恩诺沙星和磺胺二甲嘧啶联合用药机制的研究提供数据支持,并为二者的临床应用提供参考,提示新的食品安全评估应考虑药物联合暴露带来的影响。  相似文献   

19.
Chronic copper toxicity was diagnosed in a Jersey herd in the Waikato region of New Zealand following an investigation into the deaths of six cattle from a herd of 250 dry cows. Clinical signs and post-mortem examination results were consistent with a hepatopathy, and high concentrations of copper in liver and blood samples of clinically affected animals confirmed copper toxicity. Liver copper concentrations and serum gamma-glutamyl transferase activities were both raised in a group of healthy animals sampled at random from the affected herd, indicating an ongoing risk to the remaining cattle; these animals all had serum copper concentrations within normal limits. Serum samples and liver biopsies were also collected and assayed for copper from animals within two other dairy herds on the same farm; combined results from all three herds showed poor correlation between serum and liver copper concentrations.To reduce liver copper concentrations the affected herd was drenched with 0.5 g ammonium molybdate and 1 g sodium sulphate per cow for five days, and the herd was given no supplementary feed or mineral supplements. Liver biopsies were repeated 44 days after the initial biopsies (approximately 1 month after the end of the drenching program); these showed a significant 37.3% decrease in liver copper concentrations (P <0.02). Also there were no further deaths after the start of the drenching program. Since there was no control group it is impossible to quantify the effect of the drenching program in this case, and dietary changes were also made that would have depleted liver copper stores.Historical analysis of the diet was difficult due to poor record keeping, but multiple sources of copper contributed to a long term copper over supplementation of the herd; the biggest source of copper was a mineral supplement. The farmer perceived this herd to have problems with copper deficiency prior to the diagnosis of copper toxicity, so this case demonstrates the importance of monitoring herd copper status regularly. Also the poor correlation between liver and serum copper concentrations in the three herds sampled demonstrates the importance of using liver copper concentration to assess herd copper status.  相似文献   

20.
旨在探讨高铜对大鼠心肌细胞线粒体自噬的影响。将32只8月龄健康大鼠随机分为4组,每组8只,饲喂不同铜含量日粮(对照组:15 mg·kg-1;高铜Ⅰ组:30 mg·kg-1;高铜Ⅱ组:60 mg·kg-1;高铜Ⅲ组:120 mg·kg-1),连续饲喂6个月后采集心。检测心组织铜含量及其病理变化;荧光定量检测线粒体自噬相关基因LC3A、LC3B、Parkin、PINK1、p62的mRNA水平;蛋白印迹检测Parkin、PINK1、LC3B/LC3A的蛋白表达水平;免疫组化和免疫荧光检测LC3B的定位及表达。结果显示,高铜各组大鼠心组织内的铜含量均高于对照组。高铜各组出现心肌纤维排列疏松、无规则的现象。与对照组相比,高铜各组LC3A、LC3B mRNA表达量增加;高铜Ⅱ组、高铜Ⅲ组p62的mRNA表达量极显著降低;高铜各组PINK1 mRNA表达量显著升高,而Parkin mRNA的表达量有上升趋势但不显著。随着日粮中铜含量的增加,PINK1、Parkin、LC3B/LC3A的蛋白的表达量显著上调。LC3B定位于细胞质中,且高铜Ⅰ、Ⅱ、Ⅲ组LC3B表达量均显著增加。试验结果表明,高铜可诱导大鼠心肌细胞线粒体自噬的发生。  相似文献   

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