Transient receptor potential vanilloid 4 as a regulator of induced pluripotent stem cell chondrogenesis.
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2021-11
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Abstract
Transient receptor potential vanilloid 4 (TRPV4) is a polymodal calcium-permeable cation channel that is highly expressed in cartilage and is sensitive to a variety of extracellular stimuli. The expression of this channel has been associated with the process of chondrogenesis in adult stem cells as well as several cell lines. Here, we used a chondrogenic reporter (Col2a1-GFP) in murine induced pluripotent stem cells (iPSCs) to examine the hypothesis that TRPV4 serves as both a marker and a regulator of chondrogenesis. Over 21 days of chondrogenesis, iPSCs showed significant increases in Trpv4 expression along with the standard chondrogenic gene markers Sox9, Acan, and Col2a1, particularly in the green fluorescent protein positive (GFP+) chondroprogenitor subpopulation. Increased gene expression for Trpv4 was also reflected by the presence of TRPV4 protein and functional Ca2+ signaling. Daily activation of TRPV4 using the specific agonist GSK1016790A resulted in significant increases in cartilaginous matrix production. An improved understanding of the role of TRPV4 in chondrogenesis may provide new insights into the development of new therapeutic approaches for diseases of cartilage, such as osteoarthritis, or channelopathies and hereditary disorders that affect cartilage during development. Harnessing the role of TRPV4 in chondrogenesis may also provide a novel approach for accelerating stem cell differentiation in functional tissue engineering of cartilage replacements for joint repair.
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Willard, Vincent P, Holly A Leddy, Daniel Palmer, Chia-Lung Wu, Wolfgang Liedtke and Farshid Guilak (2021). Transient receptor potential vanilloid 4 as a regulator of induced pluripotent stem cell chondrogenesis. Stem cells (Dayton, Ohio), 39(11). pp. 1447–1456. 10.1002/stem.3440 Retrieved from https://hdl.handle.net/10161/32199.
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Holly Leddy
Holly A. Leddy, PhD
Holly Leddy holds a PhD in biomedical engineering from Duke University and an BA in biology from Bowdoin College. She is currently the Assistant Director of the Shared Materials and Instrumentation Facility (SMIF) at Duke University, where she leads both the Outreach and the Characterization teams. She has expertise in many types of microscopy and worked for many years in the field of cartilage mechanobiology. She has also created a vibrant outreach program at SMIF that brings the excitement of nanoscale science to thousands of people annually through both virtual and hands-on experiences.
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