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抗菌肽LL-37的原核表达、纯化及其对白色念珠菌的抑制作用

[Prokaryotic expression and purification of antimicrobial peptide LL-37 and the inhibiting effect against Candida albicans].

作者信息

Huo Y, Wang F, Sun B, Yin L R, Zhang P P, Zhang Y J, Zhang B M

机构信息

Department of Family Planning, the Second Hospital of Tianjin Medical University, Tianjin 300211, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2016 Feb;51(2):120-5. doi: 10.3760/cma.j.issn.0529-567X.2016.02.008.

Abstract

OBJECTIVE

To study the inhibitory effect of antimicrobial peptide LL-37 on Candida albicans through its ability to promote the secretion of immune factors by vaginal epithelial cells.

METHODS

(1) LL-37 prokaryotic expression vector pET-Duet/LL-37 was constructed and its expression was induced in Escherichia coli M15. The expressed LL-37 fusion protein was purified and identified by western blot. Antifungal activity of the purified protein was initially identified by Kirby-Bauer (K-B) method. (2) Purified LL-37 protein was added to human vaginal epithelial cells co-cultured with Candida, and inhibitory effect on Candida growth was determined by the glucose consumption method. Interferon γ (IFN-γ), interleukin 10 (IL-10) concentration and IFN-γ/IL-10 ratio were measured by ELISA at different time points.

RESULTS

(1) LL-37 fusion protein was purified to 96% purity at a concentration of 433.92 μg/ml, and was shown to possess anti-fungal activity confirmed by the K-B method. (2) A Candida-vaginal epithelial cells co-culture system was successfully constructed. LL-37 recombinant protein inhibited the growth of Candida with absorbance values significantly higher in the treatment group compared to the control group at all measured time points (12-hour: 3.008±0.003 versus 2.967±0.003, 24-hour: 2.941±0.003 versus 2.601±0.003, 48-hour: 2.893 ± 0.004 versus 2.409 ± 0.003; all P<0.01). Furthermore, the rate of decrease was also much slower compared to the control group. In both control and experimental groups, IFN-γ and IL-10 secretion levels were observed to rise at first peaking at 24 hours and subsequently decrease. For each time period, IFN-γ concentration in the experimental group was significantly higher at 24 hours compared to the control group [(104.00 ± 1.07) versus (85.17 ± 0.28) pg/ml,P<0.01]. In contrast, IL-10 concentrations were significantly lower than the control group at all time points (P<0.01). IFN-γ/IL-10 ratio was also observed to be significantly higher than the control group at all measured time points (P<0.01).

CONCLUSIONS

(1) Recombinant protein LL-37 could significantly inhibit the growth of Candida. (2) By influencing the secretion of immune factors such as IFN-γ, IL-10, etc, recombinant protein LL-37 is able to adjust vaginal epithelial cells local immunity, and enhance resistance to Candida infection.

摘要

目的

通过抗菌肽LL - 37促进阴道上皮细胞分泌免疫因子的能力,研究其对白色念珠菌的抑制作用。

方法

(1)构建LL - 37原核表达载体pET - Duet/LL - 37,并在大肠杆菌M15中诱导表达。对表达的LL - 37融合蛋白进行纯化,并用蛋白质免疫印迹法进行鉴定。采用K - B法初步鉴定纯化蛋白的抗真菌活性。(2)将纯化的LL - 37蛋白加入与念珠菌共培养的人阴道上皮细胞中,采用葡萄糖消耗法测定其对念珠菌生长的抑制作用。在不同时间点用酶联免疫吸附测定法(ELISA)检测干扰素γ(IFN - γ)、白细胞介素10(IL - 10)浓度及IFN - γ/IL - 10比值。

结果

(1)LL - 37融合蛋白纯化后纯度达96%,浓度为433.92μg/ml,K - B法证实其具有抗真菌活性。(2)成功构建念珠菌 - 阴道上皮细胞共培养体系。LL - 37重组蛋白抑制念珠菌生长,在所有检测时间点,治疗组吸光度值均显著高于对照组(12小时:3.008±0.003对2.967±0.003,24小时:2.941±0.003对2.601±0.003,48小时:2.893±0.004对2.409±0.003;均P<0.01)。此外,下降速率也比对照组慢得多。在对照组和实验组中,均观察到IFN - γ和IL - 10分泌水平先升高,在24小时达到峰值,随后下降。在每个时间段,实验组24小时的IFN - γ浓度均显著高于对照组[(104.00±1.07)对(85.17±0.28)pg/ml,P<0.01]。相反,IL - 10浓度在所有时间点均显著低于对照组(P<0.01)。在所有检测时间点,IFN - γ/IL - 10比值也显著高于对照组(P<0.01)。

结论

(1)重组蛋白LL - 37可显著抑制念珠菌生长。(2)重组蛋白LL - 37通过影响IFN - γ、IL - 10等免疫因子的分泌,能够调节阴道上皮细胞局部免疫,增强对念珠菌感染的抵抗力。

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