Engineered sensor actuator modulator as aqueous humor outflow actuator for gene therapy of primary open-angle glaucoma.

Bibliographic Details
Title: Engineered sensor actuator modulator as aqueous humor outflow actuator for gene therapy of primary open-angle glaucoma.
Authors: Mohanty, Samarendra, Batabyal, Subrata, Idigo, Chinenye, Narcisse, Darryl, Kim, Sanghoon, Al-Saad, Houssam, Carlson, Michael, Tchedre, Kissaou, Dibas, Adnan
Source: Journal of Translational Medicine; 8/28/2024, Vol. 22 Issue 1, p1-13, 13p
Subject Terms: BILAYER lipid membranes, AQUEOUS humor, EYE infections, OPEN-angle glaucoma, INTRAOCULAR pressure
Abstract (English): Glaucoma, a blinding eye disease with optic neuropathy, is usually associated with elevated intraocular pressure (IOP). The currently available pharmacological and surgical treatments for glaucoma have significant limitations and side effects, which include systemic reactions to medications, patient non-compliance, eye infections, surgical device failure, and damage to the eye. Here, we present Sensor-Actuator-Modulator (SAM), an engineered double mutant version of the bacterial stretch-activated mechanosensitive channel of large conductance (MscL) that directly senses tension in the membrane lipid bilayer of cells and in response, transiently opens its large nonspecific pore to release cytoplasmic fluid. The heterologously expressed mechanosensitive SAM channel acts as a tension-activated pressure release valve in trabeculocytes. In the trabecular meshwork (TM), SAM is activated by membrane stretch caused by elevated IOP. We have identified several SAM variants that are activated at physiologically relevant pressures. Using this barogenetic technology, we have demonstrated that SAM is functional in cultured TM cells, and successfully transduced in vivo in TM cells by use of AAV2/8. Further, it is effective in enhancing aqueous humor outflow facility leading to lowering the IOP in a mouse model of ocular hypertension. [ABSTRACT FROM AUTHOR]
Abstract (French): One sentence summary: Autoregulation of intraocular pressure via expression of a mechanosensitive channel of large conductance in trabecular meshwork serves as a mutation-agnostic gene therapy for glaucoma. [ABSTRACT FROM AUTHOR]
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Database: Complementary Index
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ISSN:14795876
DOI:10.1186/s12967-024-05581-1
Published in:Journal of Translational Medicine
Language:English