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肌肉特异性启动子用于基因治疗 - 增殖细胞和分化细胞的比较研究。

Muscle Specific Promotors for Gene Therapy - A Comparative Study in Proliferating and Differentiated Cells.

机构信息

Department of Human Medicine, Institute of Virology and Microbiology, Center for Biomedical Education and Research (ZBAF), Faculty of Health, Witten/Herdecke University, Witten, Germany.

Department of Neurology, University Hospital Bergmannsheil, Heimer Institute for Muscle Research, Bochum, Germany.

出版信息

J Neuromuscul Dis. 2023;10(4):575-592. doi: 10.3233/JND-221574.

Abstract

BACKGROUND

Depending on the therapy approach and disease background, the heterogeneity of muscular tissues complicates the development of targeted gene therapy, where either expression in all muscle types or restriction to only one muscle type is warranted. Muscle specificity can be achieved using promotors mediating tissue specific and sustained physiological expression in the desired muscle types but limited activity in non-targeted tissue. Several muscle specific promotors have been described, but direct comparisons between them are lacking.

OBJECTIVE

Here we present a direct comparison of muscle specific Desmin-, MHCK7, microRNA206- and Calpain3 promotor.

METHODS

To directly compare these muscle specific promotors we utilized transfection of reporter plasmids using an in vitro model based on electrical pulse stimulation (EPS) to provoke sarcomere formation in 2D cell culture for quantification of promotor activities in far differentiated mouse and human myotubes.

RESULTS

We found that Desmin- and MHCK7 promotors showed stronger reporter gene expression levels in proliferating and differentiated myogenic cell lines than miR206 and CAPN3 promotor. However, Desmin and MHCK7 promotor promoted gene expression also cardiac cells whereas miR206 and CAPN3 promotor expression was restricted to skeletal muscle.

CONCLUSIONS

Our results provides direct comparison of muscle specific promotors with regard to expression strengths and specificity as this is important feature to avoid undesired transgene expression in non-target muscle cells for a desired therapy approach.

摘要

背景

根据治疗方法和疾病背景的不同,肌肉组织的异质性使靶向基因治疗的发展变得复杂,靶向基因治疗需要在所有肌肉类型中表达或仅在一种肌肉类型中表达。可以使用启动子来实现肌肉特异性,启动子介导组织特异性和在所需肌肉类型中的持续生理表达,但在非靶向组织中的活性有限。已经描述了几种肌肉特异性启动子,但缺乏它们之间的直接比较。

目的

本文直接比较了肌特异性结蛋白(Desmin)、肌细胞特异性激活蛋白激酶 7(MHCK7)、微小 RNA206(miR206)和钙蛋白酶 3(Calpain3)启动子。

方法

为了直接比较这些肌肉特异性启动子,我们利用转染报告质粒,使用基于电脉冲刺激(EPS)的体外模型在 2D 细胞培养中诱导肌节形成,以量化在远分化的小鼠和人肌管中启动子活性。

结果

我们发现,与 miR206 和 CAPN3 启动子相比,结蛋白和 MHCK7 启动子在增殖和分化的肌源性细胞系中具有更强的报告基因表达水平。然而,结蛋白和 MHCK7 启动子也促进了心肌细胞的基因表达,而 miR206 和 CAPN3 启动子的表达则局限于骨骼肌。

结论

我们的结果提供了肌肉特异性启动子在表达强度和特异性方面的直接比较,因为这是避免所需治疗方法中在非靶肌肉细胞中产生不期望的转基因表达的重要特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089a/10357164/5cd0cbe249c1/jnd-10-jnd221574-g001.jpg

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