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用于基因治疗实时体内评估的角膜生物发光小鼠的开发。

Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies.

作者信息

Fu Dun Jack, Allen Edwin H A, Hickerson Robyn P, Leslie Pedrioli Deena M, McLean W H Irwin

机构信息

Centre for Dermatology and Genetic Medicine, Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee, Scotland, UK.

School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, UK.

出版信息

Transl Vis Sci Technol. 2020 Dec 29;9(13):44. doi: 10.1167/tvst.9.13.44. eCollection 2020 Dec.

Abstract

PURPOSE

The purpose of this study was to develop and characterize a novel bioluminescence transgenic mouse model that facilitates rapid evaluation of genetic medicine delivery methods for inherited and acquired corneal diseases.

METHODS

Corneal expression of the firefly luciferase transgene () was achieved via insertion into the locus, a type I intermediate filament keratin that is exclusively expressed in the cornea, to generate the mouse. The transgene includes a multiple target cassette with human pathogenic mutations in K3 and K12.

RESULTS

The mouse exclusively expresses in the corneal epithelium under control of the keratin K12 promoter. The luc2 protein is enzymatically active, can be readily visualized, and exhibits a symmetrically consistent readout. Moreover, structural integrity of the corneal epithelium is preserved in mice that are heterozygous for the transgene ().

CONCLUSIONS

This novel mouse model represents a potentially ideal in vivo system for evaluating the efficacies of cornea-targeting gene therapies and for establishing and/or validating new delivery modalities. Importantly, the multiple targeting cassette that is included in the transgene will greatly reduce mouse numbers required for in vivo therapy evaluation.

摘要

目的

本研究的目的是开发并表征一种新型生物发光转基因小鼠模型,该模型有助于快速评估遗传性和获得性角膜疾病的基因药物递送方法。

方法

通过将萤火虫荧光素酶转基因()插入基因座,一种仅在角膜中表达的I型中间丝角蛋白,实现萤火虫荧光素酶转基因在角膜中的表达,从而产生小鼠。该转基因包括一个在K3和K12中带有人类致病突变的多靶点盒。

结果

小鼠在角蛋白K12启动子的控制下,仅在角膜上皮中表达。luc2蛋白具有酶活性,易于可视化,并呈现出对称一致的读数。此外,对于转基因()杂合的小鼠,角膜上皮的结构完整性得以保留。

结论

这种新型小鼠模型代表了一种潜在的理想体内系统,用于评估角膜靶向基因治疗的疗效以及建立和/或验证新的递送方式。重要的是,转基因中包含的多靶点盒将大大减少体内治疗评估所需的小鼠数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fcc/7774114/b8c0d2fc1bd8/tvst-9-13-44-f001.jpg

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