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Lei Cai

 

 

 

2015 SNI Interdisciplinary Scholars

Lei Cai, Stanford Neurosciences Institute

Lei Cai

SNI Interdisciplinary Scholar, Postdoctoral Research Fellow
Department of Materials Science & Engineering

 


Bio

Lei Cai is a postdoctoral fellow with Sarah Heilshorn in the Department of Materials Science and Engineering. He received PhD in Polymer Engineering from The University of Tennessee in August 2012. The goal of his research is to combine peptide and protein motifs with synthetic macromolecules to design novel injectable hydrogels that protect cells during transplantation and promote subsequent cell maintenance and functions, thereby enabling cell-based therapy of spinal cord injury.

Faculty Advisors

Sarah Heilshorn (Materials Science & Engineering), Giles Plant (Neurosurgery), and James Weimann (Neurosurgery)

Abstract

Enabling Cell-based Therapy of Spinal Cord Injury Through Injectable Hydrogels

Spinal cord injury (SCI) causes permanent damage to about 12,000 new patients in the US each year, primarily young adults. A common result of SCI is paralysis, and unfortunately, less than 1% of SCI patients have full neurological recovery by the time of hospital discharge. To develop a regenerative therapy for SCI, many researchers have been focusing on the stem cell transplantation therapies that have resulted in partial regeneration in preclinical animal models. However, the delivery of a sufficient number of stem cells remains a difficult and unmet challenge. Only about 5% of cells survive after injection, partly due to mechanical damage. To address this problem, we have designed a very soft hydrogel that can be injected together with cells to protect cells and enhance cell survival. Following injection, we hypothesize that a hydrogel mimicking the native tissue stiffness could best support cells towards tissue regeneration. Therefore, I propose a next-generation family of hydrogels that are soft during injection to protect cells and can be tuned to have a range of stiffnesses after injection to mimic native nerve tissue. I will customize these hydrogels to deliver human induced-pluripotent stem cell-derived neural progenitors (hiPSC-NPs), which have a great potential for cell-based therapy of SCI. Using this hydrogel-based strategy, I aim to enhance hiPSC-NP survival after injection, promote neurite extension, and improve functional recovery in a rat SCI model..