School of Optometry 眼科視光學院
Home About Us What's New Subscribe eNewsletter Contact Us My School 繁體 简体 Text Only Print
About us
Message from Interim Head of School
Vision & Mission
Our People
Academic Staff
Affiliate Faculty Members
Honorary & Adjunct Professor
Visiting Staff & Academic Visitors
Optometry Clinic Staff
Research Staff
Research Students
Our Research
About us > Our People > Research Students > Ms Rong LI
Our People
Mr Samuel ABOKYI | Ms Jingfang Jennifer BIAN | Mr Shashi Kant CHAUDHARY | Mr Ka Wai Jimmy CHEUNG | Ms Sin Wan Peggy CHEUNG | Mr Man Pan Bruce CHIN | Mr Kai Yip CHOI | Mr Byung Soo Jeremy KANG | Ms Yamunadevi LAKSHMANAN | Ms Hang I Christie LAM | Mr Ki Kit LAU | Ms Hoi Lam LI | Ms Zhechuang Serena LI | Ms Sonal Aswin VYAS | Mr Kin Ken WAN | Mr Hu XIAO | Ms Ning Jenny ZHANG | Ms Biyue GUO | Ms Li PAN | Ms Qi TAN | Mr Mezbah UDDIN | Ms Meng CHENG | Mr Bing Yuan KONG | Ms Rong LI | Ms Yuanyuan LIANG | Ms Anqi LYU | Mr Ying Hon SZE | Ms Qin WANG | Ms Seema BANERJEE | Ms Hangyu ZHANG | Ms Wei YANG | Ms Mei ZHAO | Ms Yajing YANG

Ms Rong LI

Ms Rong LI

Title of project:
Exploring the functional role of CD33 in a mouse model of retinitis pigmentosa

Retinitis pigmentosa (RP) is an inherited eye disease that causes the progressive degeneration of photoreceptor cells in the retina and subsequent severe vision impairment. There are no effective treatments available to reverse the disease. It has been reported that microglia-mediated neuroinflammation contributes to neurodegeneration in RP. Therefore, reducing the microglia-mediated neuroinflammation in RP could be a meaningful therapeutic approach for RP patients.

The transmembrane protein CD33, one of the sialic acid-binding immunoglobulin (Ig) like family, is extensively expressed in microglia in the brain and regulates innate immunity. Sialic acid containing glycans and glycolipids adhered in the surface of mammalian cells and immune cells can distinguish themselves from others via CD33 by blinding to these kinds of endogenous glycans and glycolipids. Recent genome-wide association studies have identified CD33 as a risk factor for Alzheimer's disease (AD). CD33 is reported to contribute to the pathogenesis of AD by impairing microglial phagocytosis. However, the functional role of CD33 in RP remains unknown.

In this study, we would like to explore the important function of CD33 in regulating neuroinflammation and photoreceptor apoptosis in a mouse model of RP with hope to develop a novel therapeutic approach centered around CD33 inhibition for the treatment of RP patients