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纸质出版:2010
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李芙蓉,王跃.双歧杆菌脂磷壁酸对B16荷瘤小鼠Fas/FasL表达的影响[J].陆军军医大学学报(原第三军医大学学报),2010,32(12):1308-1311.
Li Furong,Wang Yue.Effects of lipoteichoic acid of bifidobacterium on Fas/FasL expression in B16 tumor-bearing mice[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(12):1308-1311.
目的 探讨双歧杆菌脂磷壁酸(lipoteichoic acid of bifidobacterium,BLTA)对黑色素瘤B16小鼠Fas/FasL表达的影响。 方法 将黑色素瘤B16细胞接种于C57BL/6小鼠(n=40)皮下,待触及肿块后于荷瘤小鼠瘤周注射不同剂量的BLTA。实验动物分为4组,每组10只:生理盐水(对照)组、低浓度BLTA(50 mg/L BLTA)组、中浓度BLTA(100 mg/L BLTA)组、高浓度BLTA(150 mg/L BLTA)组。采用MTT法检测荷瘤小鼠CTL杀伤活性;免疫组织化学染色检测肿瘤组织浸润的CD4
+
、CD8
+
淋巴细胞的表达情况;用RT-PCR检测肿瘤组织和脾脏组织Fas、FasL mRNA 的表达变化;免疫组织化学染色和Western blot检测肿瘤组织和脾脏淋巴细胞Fas、FasL 蛋白的表达变化。 结果 与对照组比较,BLTA处理各组荷瘤小鼠的CTL杀伤率明显增加(P0.05),肿瘤组织内Fas、FasL mRNA和蛋白表达明显增加(P0.05),而荷瘤小鼠脾脏组织的Fas 、FasL mRNA和蛋白表达明显下调(P0.05),肿瘤组织内CD8
+
淋巴细胞的浸润增多(P0.05),并具有剂量依赖性。 CD4
+
淋巴细胞的浸润无明显增加(P0.05)。 结论 BLTA能够通过调节Fas/FasL系统,增强CTL细胞的杀伤活性,促进肿瘤细胞的凋亡,逆转荷瘤小鼠的肿瘤免疫逃逸现象,进而提高机体的抗肿瘤作用。
Objective To investigate the effect of lipoteichoic acid of bifidobacterium (BLTA) on the expressions of Fas/FasL in bearing melanoma B16 cancer mice. Methods Forty C57BL/6 mice were randomly divided into 4 groups (n=10)
normal saline group (NS group)
low-dose BLTA group (50 mg/L)
middledose BLTA group (100 mg/L)
and highdose BLTA group (150 mg/L). Melanoma
B16 cells (0.2 ml 5×10
9
/L) were subcutaneously injected into the mice of the later 3 groups
and then
0.2 ml BLTA at corresponding doses was injected subcutaneously at the sites around the mass once a day for 10 d when the tumor (at least 2 mm×2 mm) was palpable. The NS group was given normal saline at same volume as in BLTA group. The changes of the killing activity of CTL was examined by MTT assay. The expression of the tumor-infiltrating CD4
+
and CD8
+
lymphocytes in tumor tissue were detected by immunohistochemistry. RT-PCR was used to detect the mRNA expression variance of the Fas and FasL in tumor and spleen tissue. The protein expression of Fas
FasL in tumor tissue and lymphocytes of spleen were detected by immunohistochemistry and Western blotting. Results Compared with the control group
BLTA significantly improved the CTL killing activity (P0.05). The mRNA and protein expression of Fas and FasL were significantly up-regulated in the tumor tissue (P0.05) whereas they were downregulated in spleen tissue (P0.05). There were significantly more CD8+ lymphocyte infiltration in the tumor tissue in a dose-dependent manner (P0.05)
however
the infiltration of CD4+ lymphocyte was not significantly increased(P0.05). Conclusion BLTA enhances the killing activity of CTL by regulating Fas/FasL system
and thus
promotes apoptosis of tumor cells to suppress tumor immune escape in tumor-bearing mice
thereby it exerts anti-tumor effect further.
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