Use of human pluripotent stem cells to define initiating molecular mechanisms of cataract for anti-cataract drug discovery

Chitra Umala Dewi, Michael D. O’Connor

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Cataract is a leading cause of blindness worldwide. Currently, restoration of vision in cataract patients requires surgical removal of the cataract. Due to the large and increasing number of cataract patients, the annual cost of surgical cataract treatment amounts to billions of dollars. Limited access to functional human lens tissue during the early stages of cataract formation has hampered efforts to develop effective anti-cataract drugs. The ability of human pluripotent stem (PS) cells to make large numbers of normal or diseased human cell types raises the possibility that human PS cells may provide a new avenue for defining the molecular mechanisms responsible for different types of human cataract. Towards this end, methods have been established to differentiate human PS cells into both lens cells and transparent, light-focusing human micro-lenses. Sensitive and quantitative assays to measure light transmittance and focusing ability of human PS cell-derived micro-lenses have also been developed. This review will, therefore, examine how human PS cell-derived lens cells and micro-lenses might provide a new avenue for development of much-needed drugs to treat human cataract.
Original languageEnglish
Article number1269
Number of pages11
JournalCells
Volume8
Issue number10
DOIs
Publication statusPublished - 2019

Open Access - Access Right Statement

© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Keywords

  • cataract
  • lenses
  • pluripotent stem cells

Fingerprint

Dive into the research topics of 'Use of human pluripotent stem cells to define initiating molecular mechanisms of cataract for anti-cataract drug discovery'. Together they form a unique fingerprint.

Cite this