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自我互补腺相关病毒6型介导的ADAMTS4基因敲低可长期有效增强退变人髓核细胞中聚集蛋白聚糖:一种治疗椎间盘疾病的新方法。

Self-complementary adeno-associated virus serotype 6 mediated knockdown of ADAMTS4 induces long-term and effective enhancement of aggrecan in degenerative human nucleus pulposus cells: A new therapeutic approach for intervertebral disc disorders.

作者信息

Mern Demissew Shenegelegn, Tschugg Anja, Hartmann Sebastian, Thomé Claudius

机构信息

Department of Neurosurgery, Innsbruck Medical University, Innsbruck, Austria.

出版信息

PLoS One. 2017 Feb 16;12(2):e0172181. doi: 10.1371/journal.pone.0172181. eCollection 2017.

Abstract

Inhibition of intervertebral disc (IVD) degeneration, which is often accompanied by painful inflammatory and immunopathological processes, is challenging. Current IVD gene therapeutic approaches are based on adenoviral gene delivery systems, which are limited by immune reactions to their viral proteins. Their applications in IVDs near to sensitive neural structure could provoke toxicity and immunological side-effects with neurological deficits. Self-complementary adeno-associated virus (scAAV) vectors, which do not express any viral gene and are not linked with any known disease in humans, are attractive therapeutic gene delivery vectors in degenerative IVDs. However, scAAV-based silencing of catabolic or inflammatory factor has not yet been investigated in human IVD cells. Therefore, we used scAAV6, the most suitable serotype for transduction of human nucleus pulposus (NP) cells, to knockdown the major catabolic gene (ADAMTS4) of IVD degeneration. IVD degeneration grades were determined by preoperative magnetic resonance imaging. Lumbar NP tissues of degeneration grade III were removed from 12 patients by nucleotomy. NP cells were isolated and cultured with low-glucose. Titre of recombinant scAAV6 vectors targeting ADAMTS4, transduction efficiencies, transduction units, cell viabilities and expression levels of target genes were analysed using quantitative PCR, fluorescence microscopy, fluorescence-activated cell sorting, 3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide assays, quantitative reverse transcription PCR, western blot and enzyme-linked immunosorbent assays during 48 days of post-transduction. Transduction efficiencies between 98.2% and 37.4% and transduction units between 611 and 245 TU/cell were verified during 48 days of post-transduction (p<0.001). scAAV6-mediated knockdown of ADAMTS4 with maximum 87.7% and minimum 40.1% was confirmed on day 8 and 48 with enhanced the level of aggrecan 48.5% and 30.2% respectively (p<0.001). scAAV6-mediated knockdown of ADAMTS4 showed no impact on cell viability and expression levels of other inflammatory catabolic proteins. Thus, our results are promising and may help to design long-term and less immunogenic gene therapeutic approaches in IVD disorders, which usually need prolonged therapeutic period between weeks and months.

摘要

抑制椎间盘(IVD)退变具有挑战性,因为其常伴有疼痛性炎症和免疫病理过程。目前的IVD基因治疗方法基于腺病毒基因递送系统,该系统受限于对其病毒蛋白的免疫反应。它们在靠近敏感神经结构的IVD中的应用可能引发毒性和免疫副作用,并导致神经功能缺损。自我互补腺相关病毒(scAAV)载体不表达任何病毒基因,且与人类任何已知疾病均无关联,是用于退变IVD的有吸引力的治疗性基因递送载体。然而,基于scAAV的分解代谢或炎症因子沉默在人IVD细胞中尚未得到研究。因此,我们使用最适合转导人髓核(NP)细胞的血清型scAAV6,来敲低IVD退变的主要分解代谢基因(ADAMTS4)。IVD退变分级通过术前磁共振成像确定。通过髓核切除术从12例患者中获取退变分级为III级 的腰椎NP组织。分离NP细胞并在低糖条件下培养。在转导后48天内,使用定量PCR、荧光显微镜、荧光激活细胞分选、3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐法、定量逆转录PCR、蛋白质印迹和酶联免疫吸附测定法分析靶向ADAMTS4的重组scAAV6载体的滴度、转导效率、转导单位、细胞活力和靶基因表达水平。在转导后48天内,验证了转导效率在98.2%至37.4%之间,转导单位在611至245 TU/细胞之间(p<0.001)。在第8天和第48天证实scAAV6介导的ADAMTS4敲低率最高为87.7%,最低为40.1%,同时聚集蛋白聚糖水平分别提高了48.5%和30.2%(p<0.001)。scAAV6介导的ADAMTS4敲低对细胞活力和其他炎症分解代谢蛋白的表达水平没有影响。因此,我们的结果很有前景,可能有助于设计针对IVD疾病的长期且免疫原性较低的基因治疗方法,IVD疾病通常需要数周 至数月的延长治疗期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e93c/5313142/ee2a98388178/pone.0172181.g001.jpg

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