Dr. Sayan Basu

The Cornea Institute, LV. Prasad Eye Institute, Hyderabad, India

1 article

Dr. Sayan Basu is the Director, Prof. Brien Holden Eye Research Centre, Prof D Balasubramanian Chair of Eye Research, Director, Centre for Ocular Regeneration (CORE) & Virender Sangwan Chair of Regenerative Ophthalmology, LVPEI, Adjunct Associate Professor of Ophthalmology, School of Medicine and Dentistry, University of Rochester, New York, USA. Dr. Basu has received the Achievement Award from the American Academy of Ophthalmology and serves on the editorial board of several prestigious scientific journals such as the British Journal of Ophthalmology, The Ocular Surface, Seminars in Ophthalmology, Current Eye Research, and Indian Journal of Ophthalmology. He has published numerous highly cited papers and is held in high regard as a researcher by the ophthalmology and visual sciences community. He currently heads all research activities at LVPEI, and his specific research interests include developing novel therapies for dry eye disease, scarless corneal wound healing and stem cell therapies with renowned national and international collaborators.

  1. Articles 5 May 2021 23 min read

    Simple Limbal Epithelial Transplantation: A Review

    I. Introduction The cornea is lined by non-keratinized, stratified squamous epithelium. At the limbus, there is a gradual transition of these cells to non-keratinized, stratified columnar epithelial cells, along with mucin-secreting goblet cells, forming the conjunctival epithelium. The corneoscleral limbus lies between these two epithelia in a healthy eye. The limbus contains palisades of Vogt, the basal layer of which function as a repository for the corneal epithelial stem cells.(1, 2) These limbal epithelial stem cells (LESC’s) divide whenever the corneal epithelium is required to be replenished. As the stem cells divide, one of the daughter cells retains the primitive nature of the parent cell and functions to maintain the stem cell pool. The other daughter stem cell differentiates to acquire the physiological nature of a specific tissue, like the corneal epithelium. These cells are known as ‘transient amplifying cells’, which then divide and migrate centripetally, circumferential