| Literature DB >> 26615056 |
Karen Y Torrejon1, Ellen L Papke1, Justin R Halman1, Judith Stolwijk1, Cula N Dautriche1, Magnus Bergkvist1, John Danias2, Susan T Sharfstein1, Yubing Xie3.
Abstract
Intraocular pressure (IOP) is mostly regulated by aqueous humor outflow through the human trabecular meshwork (HTM) and represents the only modifiable risk factor of glaucoma. The lack of IOP-modulating therapeutics that targets HTM underscores the need of engineering HTM for understanding the outflow physiology and glaucoma pathology in vitro. Using a 3D HTM model that allows for regulation of outflow in response to a pharmacologic steroid, a fibrotic state has been induced resembling that of glaucomatous HTM. This disease model exhibits HTM marker expression, ECM overproduction, impaired HTM cell phagocytic activity and outflow resistance, which represent characteristics found in steroid-induced glaucoma. In particular, steroid-induced ECM alterations in the glaucomatous model can be modified by a ROCK inhibitor. Altogether, this work presents a novel in vitro disease model that allows for physiological and pathological studies pertaining to regulating outflow, leading to improved understanding of steroid-induced glaucoma and accelerated discovery of new therapeutic targets. Biotechnol. Bioeng. 2016;113: 1357-1368.Entities:
Keywords: 3D culture; SU-8; intraocular pressure; outflow; steroid-induced glaucoma; trabecular meshwork
Mesh:
Year: 2015 PMID: 26615056 PMCID: PMC4854669 DOI: 10.1002/bit.25899
Source DB: PubMed Journal: Biotechnol Bioeng ISSN: 0006-3592 Impact factor: 4.530