目的 用慢病毒介导的方法抑制白细胞介素-10(IL-10)的RNA,观察IL-10通过乙二醛酶1(GLO1)影响大鼠脊髓损伤后运动功能恢复。 方法 SD大鼠66只,采用Allen’s法制备脊髓钝挫伤(spinal cord contusion,SCC)模型,随机分为Sham组(n=9)、SCC组(n=27)、Vector组(n=15)和IL-10 SH组(n=15),分别注射空质粒和包装IL-10 siRNA的质粒;每组再分为3 d、7 d和28 d 亚组。采用BBB(Basso,Beattie,Bresnahan)评分评估大鼠后肢运动功能;免疫组织化学和qRT-PCR技术定位和定量测定IL-10和GLO1的表达变化;用慢病毒包装的RNA构建IL-10的RNA干扰模型(IL-10-SH-LV)评估IL-10和GLO1在脊髓损伤后的功能,GeneMANIA生物信息学预测IL-10和GLO1的关系。 结果 SCC后大鼠双后肢截瘫,后肢运动功能消失,BBB评分在损伤后1 d,3 d,7 d,14 d逐渐恢复,但低于对照组。qRT-PCR结果显示IL-10在脊髓损伤后表达显著降低;SCC后,免疫组织化学结果显示IL-10主要在脊髓前角的神经元和神经胶质细胞中表达。慢病毒干扰IL-10的表达后,随着时间推移,GLO1表达增加,大鼠运动功能BBB评分也逐渐恢复。GeneMANIA结果显示GLO1和IL-10通过共表达的Hpd和Klk1c2、Kcns1、Proc相互作用。 结论 IL-10通过上调抗氧化应激因子GLO1的表达促进脊髓损伤大鼠运动功能恢复。
Abstract
Objective To inhibit the expression of IL-10 and to observe IL-10 affected the recovery of motor function of spinal cord contusion rats by glyoxalase-1 by using lentivirus mediated RNA. Methods The model of spinal cord contusion (SCC) was established in 66 Sprague-Dawley rats with Allen's method. The rats were randomized into a Sham group (n=9); a SCC group (n=27)、a Vector group (n=15) and a IL-10 SH group (n=15), which were injected blank lentivirus vector and vector of IL-10 siRNA respectively and then divided into 3 days, 7 days and 28 days subgroups. Basso, Beattie, Bresnahan (BBB) score was used to evaluate the motor function recovery of hind limbs in rats. The localization and expression of GLO1 were examined by immunohistochemistry and real-time quantitative polymerase chain reaction (qRT-PCR) respectively. The inhibition of IL-10 (IL-10-SH-LV) mediated by lentivirus transduction was used to elucidate the function of IL-10 and GLO1. GeneMANIA was used to predict the relationship between IL-10 and GLO1. Results The motor capability of hind limbs disappeared after SCC and followed by recovery at 1d, 3d, 7d and 14d as evaluated by BBB score, but it still could not reach the normal level. The expression of IL-10 decreased obviously in spinal cord tissue after SCC was detected by qRT-PCR, and the immunoreactive positive reactant of IL-10 was located in neurons and neuroglial cells of ventral horn in spinal cord by immunofluorescence. Inhibition of IL-10 mediated by lentivirus reduced motor function (evaluated by BBB score), but increased in the next time with the upregulation of GLO1. Futher more, GeneMANIA result showed that GLO1 contacted with IL-10 through Hpd and Klk1c2/Kcns1/Proc, which were co-expression in rats. Conclusions IL-10 promotes functional recovery of spinal cord contusion rats, which may be associated with upregulation of GLO1.
关键词
白细胞介素-10 /
乙二醛酶1 /
RNAi /
大鼠 /
脊髓钝挫伤
Key words
IL-10; GLO1 /
RNAi; Rats; Spinal cord contusion
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参考文献
[1] Li XZ, Nie Z, Yang Q, et al. Effect of valproic acid on oxidative stress after acute spinal cord injury in rats[J]. Orthopedic Journal of China, 2012, 20(14): 1323-1327.
[2] Liu Q, Xia YZ, Yan Y. Protease activated receptor 2(PAR2) regulates GFAP and vimentin expression at the early stage of glia scar formation after spinal cord injury[J]. Chinese Journal of Nervous and Mental Diseases, 2013, 39(7): 421-426.
[3] Rowland JW, Hawryluk GW, Kwon B, et al. Current status of acute spinal cord injury pathophysiology and emerging therapies: promise on the horizon[J]. Neurosurg Focus, 2008, 25(5): E2. DOI: 10.3171/FOC.2008.25.11.E2.
[4] Knoller N, Auerbach G, Fulga V, et al. Clinical experience using incubated autologous macrophages as a treatment for complete spinal cord injury: phase I study results[J]. J Neurosurg Spine, 2005, 3(3): 173-181. DOI: 10.3171/spi.2005.3.3.0173.
[5] Bethea JR, Nagashima H, Acosta MC, et al. Systemically administered IL-10 reduces TNF-α production and significantly improves functional recovery following traumatic spinal cord injury in rats[J]. J Neurotrauma, 1999, 16(10): 851-863. DOI: 10.1089/neu.1999.16.851.
[6] Octavio JG, Javier C, Antonio I, et al. Early effects of modulating nuclear factor-kB activation on traumatic spinal cord injury in rats[J]. Ann N Y Acad Sci, 2005, 1053(1): 148-150. DOI: 10.1196/annals.1344.012.
[7] Rulli A, Antognelli C, Prezzi E, et al. A possible regulatory roleof 17beta-estradiol and tamoxifen on glyoxalase I and glyoxalase II genes expression in MCF7 and BT20 human breast cancer cells[J]. Breast Cancer Res Treat, 2006, 96(2): 187-196. DOI: 10.1007/s10549-005-9078-7.
[8] Kim KM, Kim YS, Jung DH, et al. Increased glyoxalase I levels inhibit accumulation of oxidative stress and an advanced glycation end product in mouse mesangial cells cultured in high glucose[J]. Exp Cell Res, 2012, 318(2): 152-159. DOI: 10.1016/j.yexcr.2011.10.013.
[9] Cheng WL, Tsai MM, Tsai CY, et al. Glyoxalase-I is a novel prognosis factor associated with gastric cancer progression[J]. PLoS One, 2012, 7(3): e34352. DOI: 10.1371/journal.pone.0034352.
[10] Megan J, Douglas W. Role of advanced glycation endproducts and glyoxalase I in diabetic peripheral sensory neuropathy[J]. Transl Res, 2012, 159(5): 355-365. DOI: 10.1016/j.trsl.2011.12.004.
[11] Bethea JR, Dietrich WD. Targeting the host inflammatory response in traumatic spinal cord injury[J]. Curr Opin Neurol, 2002, 15(3):355-360. DOI: 10.1097/00019052-200206000-00021.
[12] Ndisang JF, Vannacci A, Rastogi S. Oxidative stress and inflammation in obesity, diabetes, hypertension, and related cardiometabolic complications[J]. Oxid Med Cell Longev, 2014, 2014(S): 506948. DOI: 10.1155/2014/506948.
[13] Hellenbrand DJ, Reichl KA, Travis BJ, et al. Sustained interleukin-10 delivery reduces inflammation and improves motor function after spinal cord injury[J]. J Neuroinflammation, 2019, 16(1): 93-107. DOI: 10.1186/s12974-019-1479-3.
[14]Koushki D, Latifi S, Javidan AN, et al. Efficacy of some non-conventional herbal medications (sulforaphane, tanshinone IIA, and tetramethylpyrazine) in inducing neuroprotection in comparison with interleukin-10 after spinal cord injury: a meta-analysis[J]. J Spinal Cord Med, 2015, 38(1): 13-22. DOI: 10.1179/2045772314Y. 0000000 215.
[15]Badner A, Vidal PM, Hong J, et al. Endogenous interleukin-10 deficiency exacerbates vascular pathology in traumatic cervical spinal cord injury[J]. J Neurotrauma, 2019, 36(15): 2298-2307. DOI: 10.1089/neu.2018.6081.
[16] Ni GY, Chen S, Yuan JW, et al. Comparative proteomic study reveals the enhanced immune response with the blockade of interleukin 10 with anti-IL-10 and anti-IL-10 receptor antibodies in human U937 cells[J]. PloS One, 2019, 14(3): e0213813. DOI: 10.1371/journal.pone.0213813.
[17]Brewer KL, Bethea JR, Yezierski RP. Neuropretective effects of interleukin-10 following excitotoxic spinal cord injury[J]. Exp Neurol, 1999, 159(2): 484-493. DOI: 10.1006/exnr.1999.7173.
[18]Oruckaptan HH, Ozisik P, Atilla P, et al. Systemic administration of interleukin-10 attenuates early ischemic response following spinal cord ischemia reperfusion injury in rats[J]. J Surg Res, 2009, 155(2): 345-356. DOI: 10.1016/j.jss.2008.07.013.
基金
四川省大学生创新创业训练项目(201813705061)