The application of lentiviral vectors for the establishment of TGFβ2-induced ocular hypertension in C57BL/6J mice

• Published in: Experimental eye research 2022-08, Vol.221, p.109137-109137, Article 109137
• Main Authors: Peng, Michael, Margetts, Tyler J., Rayana, Naga Pradeep, Sugali, Chenna Kesavulu, Dai, Jiannong, Mao, Weiming
• Format: Article
• Language: English
• Subjects: Adenoviridae - genetics; Animals; Cytomegalovirus Infections; Female; Glaucoma, Open-Angle - chemically induced; Glaucoma, Open-Angle - genetics; Glaucoma, Open-Angle - metabolism; Intraocular Pressure; Lentivirus; Male; Mice; Mice, Inbred C57BL; Mouse model; Ocular hypertension; Ocular Hypertension - metabolism; TGFβ2; Trabecular meshwork; Trabecular Meshwork - metabolism; Transforming Growth Factor beta2 - metabolism
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1016/j.exer.2022.109137

Elevated levels of TGFβ2 in the aqueous humor is associated with the pathological changes in the trabecular meshwork (TM). These changes lead to ocular hypertension (OHT), the most important risk factor for the development and progression of primary open angle glaucoma (POAG), a leading cause of blindness worldwide. Therefore, TGFβ2 is frequently used to develop OHT models including in perfusion cultured eyes and in mouse eyes. Adenovirus-mediated overexpression of human mutant TGFβ2 has demonstrated great success in increasing intraocular pressure (IOP) in mouse eyes. However, adenoviruses have limited capacity for a foreign gene, induce transient expression, and may cause ocular inflammation. Here, we explored the potential of using lentiviral vectors carrying the mutant human TGFβ2C226S/C228S (ΔhTGFβ2C226S/C228S) gene expression cassette for the induction of OHT in C57BL/6J mice. Lentiviral vectors using CMV or EF1α promoter to drive the expression of ΔhTGFβ2C226S/C228S were injected into one of the mouse eyes and the fellow eye was injected with the same vector but expressing GFP/mCherry as controls. Both intravitreal and intracameral injection routes were tested in male and female mice. We did not observe significant IOP changes using either promoter or injection route at the dose of 8 × 105 PFU/eye. Immunostaining showed normal anterior chamber angle structures and a slight increase in TGFβ2 expression in the TM of the eyes receiving intracameral viral injection but not in those receiving intravitreal viral injection. At the dose of 2 × 106 PFU/eye, intracameral injection of the lentiviral vector with the CMV-ΔhTGFβ2C226S/C228S cassette induced significant IOP elevation and increased the expression of TGFβ2 and fibronectin isoform EDA in the TM. Our data suggest that lentiviral doses are important for establishing the TGFβ2-induced OHT model in the C57BL/6J strain. •Only high doses of lentiviral TGFβ2 expression vectors induced ocular hypertension in some mouse eyes.•Increased TGFβ2 expression was observed in intracamerally injected mouse eyes.•Lentiviral transduction did not induce severe inflammation in mouse eyes.