Title Information
Title
Cartilage Derived Progenitor Cells Exhibit Paracrine Effects that Direct the Healing Process
Type of Resource (primo)
dissertations
Name: Personal
Name Part
Lin, Yu Ting
Role
Role Term: Text
creator
Name: Personal
Name Part
Jayasuriya, Chathuraka
Role
Role Term: Text
Advisor
Name: Personal
Name Part
Wei, Lei
Role
Role Term: Text
Reader
Name: Personal
Name Part
Fleming, Braden
Role
Role Term: Text
Reader
Name: Corporate
Name Part
Brown University. Department of Molecular Pharmacology, Physiology and Biotechnology
Role
Role Term: Text
sponsor
Origin Information
Copyright Date
2022
Physical Description
Extent
vii, 33 p.
digitalOrigin
born digital
Note: thesis
Thesis (Sc. M.)--Brown University, 2022
Genre (aat)
theses
Abstract
Meniscal tearing is one of the most common types of orthopedics injuries and found in people of all ages. Meniscal tearing is also a risk factor of knee osteoarthritis. Tears that occur in the inner white zone of the meniscus, which has no vascularity, presents a significant clinical challenge due to intrinsically poor healing capacity of this region. Mesenchymal stem/progenitor cell (MSC)-based repair is an emerging and effective preclinical strategy that is being explored to augment and ultimately improve clinical approaches that are commonplace for treating these injuries. Current research involving exogenous cell-based meniscus tissue repair and regeneration utilizes cells from various tissue sources, including bone marrow, adipose (fat), synovium, and cartilage. As a phenotypically similar connective tissue to meniscal fibrocartilage, articular cartilage derived progenitor cells (CPCs) have been used to stimulate meniscal tissue healing. It has been reported that CPCs have elevated expression of the transcription factor SOX9, which is central for chondrogenic matrix synthesis. However, the way CPC interact with native meniscal fibro chondrocytes to promote their cell proliferation and tissue remodeling to aid in meniscal healing remain unknown. This study examines the role of extracellular vesicles (EVs) as a potential mechanism for the observed cell mediated anabolic effects of CPCs. Our results show that CPCs do produce EVs under normal conditions. Conditioned media collected from CPC cultures stimulated increased meniscal cell migration. Further, co-culturing CPCs with meniscal fibro chondrocytes directly regulate expressions of SOX9 and aggrecan in the meniscal cells. Overall, this study provides insight into the mechanism of action of this promising progenitor cell population, which can play an active role in the cartilaginous tissue repair.
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/01763304")
Topic
Mesenchymal stem cells
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/00817187")
Topic
Articular cartilage
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/01016164")
Topic
Meniscus (Anatomy)--Wounds and injuries
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/01132975")
Topic
Stem cells
Language
Language Term (ISO639-2B)
English
Record Information
Record Content Source (marcorg)
RPB
Record Creation Date (encoding="iso8601")
20220706