B16/F10黑色素瘤伴慢性神经性疼痛的尿激酶基因敲除小鼠脑组织中尿激酶受体及纤维蛋白溶解系统其他组分水平的变化

E. Frantsiyants, V. Bandovkina, I. Kaplieva, N. Cheryarina, E. Surikova, I. Neskubina, Y. Pogorelova, L. Nemashkalova
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引用次数: 1

摘要

研究目的:B16/F10黑色素瘤单独生长和伴慢性神经性疼痛(CNP)的尿激酶基因敲除小鼠(uPA-/-)脑内尿激酶系统成分变化分析材料和方法。该研究包括男性和女性C57BL/6-PlautmI。IBug-ThisPlau6FDhu/GFDhu小鼠(uPA-/-) (n = 48)和C57BL/6小鼠(uPA+/+) (n = 80)移植B16/F10黑色素瘤单独生长和与CNP一起生长。elisa法测定动物脑组织中尿激酶受体(uPAR)和纤溶酶(PAP)的水平及pai - 1抑制剂的活性和水平。大脑中uPAR、pai - 1和PAP的水平仅在完整的uPA-/-雄性中存在差异,平均比uPA+/+小鼠高1.6倍(p < 0.05)。在CNP组中,uPA-/-雄性小鼠的PAI-I升高了1.3倍(p < 0.05), PAP降低了2.6倍(p < 0.05),而uPA+/+雄性小鼠的PAI-I和PAP变化则相反;与uPA+/+组相比,uPA-/-组各指标升高1.6 ~ 2.1倍(p < 0.05)。在仅患有黑色素瘤的动物中,uPA-/-雄性小鼠脑组织中uPAR、pai - 1和PAP水平的变化与CNP组和uPA+/+雄性小鼠不同;uPA+/+组uPAR和PAP分别升高1.7倍和3.0倍(p < 0.05), uPA-/-组仅PAP升高3.2倍(p < 0.05)。在uPA-/-小鼠中,无论性别,与使用CNP的动物相比,联合使用CNP的uPAR和pai - 1水平平均分别下调1.5倍和2.0倍(p < 0.05), PAP水平平均上调2.2倍(p < 0.05);在uPA+/+动物中,只有雄性的uPAR下降了3.7倍(p < 0.05),而所有小鼠的pai - 1增加了2.0倍(p < 0.05)。尿激酶基因敲除动物脑组织中所研究参数在应激因素下的变化表明,脑尿激酶系统在对CNP和黑色素瘤生长的反应中发挥了作用,这些变化的性别特异性可能是皮肤黑色素瘤发生风险和病程性别差异的另一个因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in levels of urokinase receptor and other components of fibrinolytic system in brain tissues in urokinase gene-knockout mice with B16/F10 melanoma growing together with chronic neurogenic pain
Purpose of the study. An analysis of the changes in components of the urokinase system in the brain of urokinase gene-knockout mice (uPA-/-) with B16/F10 melanoma growing alone and together with chronic neurogenic pain (CNP).Materials and methods. The study included male and female C57BL/6-PlautmI.IBug-ThisPlau6FDhu/GFDhu mice (uPA-/-) (n = 48) and C57BL/6 mice (uPA+/+) (n = 80) with transplanted B16/F10 melanoma growing solitarily and together with CNP. Levels of the urokinase receptor (uPAR) and plasmin (PAP) and activity and levels of the PAI-I inhibitor were measured in the brain of animals by ELISA.Results. Levels of uPAR, PAI-I and PAP in the brain differed only in intact uPA-/- males, being on average 1.6 times higher (p < 0.05) than in uPA+/+ mice. Among animals with CNP, uPA-/- males showed increased PAI-I by 1.3 times (p < 0.05) and decreased PAP by 2.6 times (p < 0.05), while in uPA+/+ males, changes in PAI-I and PAP were opposite; in uPA-/- females, levels of all indicators increased by 1.6–2.1 times (p < 0.05), unlike uPA+/+ females. Among animals with melanoma only, changes in the levels of uPAR, PAI-I and PAP in the brain tissues in uPA-/- males differed from the group with CNP and from uPA+/+ males; in uPA+/+ females, levels of uPAR and PAP increased by 1.7 and 3.0 times (p < 0.05), and only PAP increased in uPA-/- females by 3.2 times (p < 0.05). Combination of CNP with melanoma in uPA-/- mice, regardless of their gender, down-regulated levels of uPAR and PAI-I on the average by 1.5 and 2.0 times, respectively (p < 0.05), and up-regulated PAP on the average by 2.2 times (p < 0.05) compared to the levels in animals with CNP; in uPA+/+ animals, similar decline of uPAR by 3.7 times (p < 0.05) was registered only in males, and an increase of PAI-I by 2.0 times (p < 0.05) was noted in all mice.Conclusion. Changes in the studied parameters in the brain tissue of urokinase gene-knockout animals in response to stress factors indicate the role of the brain urokinase system in the response to both CNP and melanoma growth, and the gender specificity of these changes may be another factor that conditions gender differences in the risk of occurrence and course of cutaneous melanoma. 
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