华北农学报
華北農學報
화북농학보
ACTA AGRICULTURAE BOREALI-SINICA
2014年
3期
32-35
,共4页
王占美%赵园%陈健伟%国晓瞳%丛霞%姜忠玲%田文儒
王佔美%趙園%陳健偉%國曉瞳%叢霞%薑忠玲%田文儒
왕점미%조완%진건위%국효동%총하%강충령%전문유
热休克蛋白%葛根素%LLC-PK1%HSP70
熱休剋蛋白%葛根素%LLC-PK1%HSP70
열휴극단백%갈근소%LLC-PK1%HSP70
LLC-PK1%Puerarin%Heat stress%HSP70
为研究不同浓度葛根素对热应激诱导的LLC-PK1细胞HSP70 mRNA和蛋白表达的影响,筛选出葛根素诱导HSP70表达的最佳浓度。选取处于对数增长期的猪肾小管上皮细胞,分为37℃对照组和42℃热应激组,热应激组细胞先在加入不同浓度(0.01~100μmol/L不等)葛根素的培养基中培养,热应激之后,提取总RNA和总蛋白,用RT-PCR和Western Blot检测HSP70 mRNA和蛋白的相对表达量。结果显示,42℃热应激和不同浓度的葛根素均能显著诱导LLC-PK1细胞的HSP70 mRNA和蛋白的表达,并且,随葛根素浓度升高,HSP70表达量增加,在各浓度组中,10μmol/L的葛根素诱导HSP70的表达最显著(P<0.01)。上述结果证明,葛根素能够诱导热应激条件下LLC-PK1细胞 HSP70的表达,并且随葛根素浓度升高,HSP70表达量增加。
為研究不同濃度葛根素對熱應激誘導的LLC-PK1細胞HSP70 mRNA和蛋白錶達的影響,篩選齣葛根素誘導HSP70錶達的最佳濃度。選取處于對數增長期的豬腎小管上皮細胞,分為37℃對照組和42℃熱應激組,熱應激組細胞先在加入不同濃度(0.01~100μmol/L不等)葛根素的培養基中培養,熱應激之後,提取總RNA和總蛋白,用RT-PCR和Western Blot檢測HSP70 mRNA和蛋白的相對錶達量。結果顯示,42℃熱應激和不同濃度的葛根素均能顯著誘導LLC-PK1細胞的HSP70 mRNA和蛋白的錶達,併且,隨葛根素濃度升高,HSP70錶達量增加,在各濃度組中,10μmol/L的葛根素誘導HSP70的錶達最顯著(P<0.01)。上述結果證明,葛根素能夠誘導熱應激條件下LLC-PK1細胞 HSP70的錶達,併且隨葛根素濃度升高,HSP70錶達量增加。
위연구불동농도갈근소대열응격유도적LLC-PK1세포HSP70 mRNA화단백표체적영향,사선출갈근소유도HSP70표체적최가농도。선취처우대수증장기적저신소관상피세포,분위37℃대조조화42℃열응격조,열응격조세포선재가입불동농도(0.01~100μmol/L불등)갈근소적배양기중배양,열응격지후,제취총RNA화총단백,용RT-PCR화Western Blot검측HSP70 mRNA화단백적상대표체량。결과현시,42℃열응격화불동농도적갈근소균능현저유도LLC-PK1세포적HSP70 mRNA화단백적표체,병차,수갈근소농도승고,HSP70표체량증가,재각농도조중,10μmol/L적갈근소유도HSP70적표체최현저(P<0.01)。상술결과증명,갈근소능구유도열응격조건하LLC-PK1세포 HSP70적표체,병차수갈근소농도승고,HSP70표체량증가。
This experiment was to study the effect of puerarin on the thermal stress induced HSP70 expression in pig renal tubular epithelial cell (LLC-PK1),and to selected the optimal concentration of puerarin for inducing HSP70 expression. The LLC-PK1 in its logarithmic growth period was selected and divided into 37 ℃ control group and 42 ℃ heat stress group. The heat stress group of cell was incubated with various concentrations (from 0. 01-100 μmol/L ) of puerarin before the heat stress treatment,and then the total RNA and protein of the cells were ex-tracted and were detected by RT-PCR and Western Blot,respectively. The results showed that both thermal stress at 42 ℃ and puerarin with various concentrations significantly induced the HSP70 expression of LLC-PK1 (P<0. 01), and HSP70 expression increased as the puerarin concentration increased in the culture medium. The relative expres-sion of HSP70 in the heat stress group was the highest in the 10 μmol/L of puerarin group. The above results indi-cate that puerarin can induce HSP70 expression of LLC-PK1 under heat stress and this expressions increased as the puerarin concentration increased in the culture medium.