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TRPV4 as a therapeutic target for joint diseases.

Publication ,  Journal Article
McNulty, AL; Leddy, HA; Liedtke, W; Guilak, F
Published in: Naunyn Schmiedebergs Arch Pharmacol
April 2015

Biomechanical factors play a critical role in regulating the physiology as well as the pathology of multiple joint tissues and have been implicated in the pathogenesis of osteoarthritis. Therefore, the mechanisms by which cells sense and respond to mechanical signals may provide novel targets for the development of disease-modifying osteoarthritis drugs (DMOADs). Transient receptor potential vanilloid 4 (TRPV4) is a Ca(2+)-permeable cation channel that serves as a sensor of mechanical or osmotic signals in several musculoskeletal tissues, including cartilage, bone, and synovium. The importance of TRPV4 in joint homeostasis is apparent in patients harboring TRPV4 mutations, which result in the development of a spectrum of skeletal dysplasias and arthropathies. In addition, the genetic knockout of Trpv4 results in the development of osteoarthritis and decreased osteoclast function. In engineered cartilage replacements, chemical activation of TRPV4 can reproduce many of the anabolic effects of mechanical loading to accelerate tissue growth and regeneration. Overall, TRPV4 plays a key role in transducing mechanical, pain, and inflammatory signals within joint tissues and thus is an attractive therapeutic target to modulate the effects of joint diseases. In pathological conditions in the joint, when the delicate balance of TRPV4 activity is altered, a variety of different tools could be utilized to directly or indirectly target TRPV4 activity.

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Published In

Naunyn Schmiedebergs Arch Pharmacol

DOI

EISSN

1432-1912

Publication Date

April 2015

Volume

388

Issue

4

Start / End Page

437 / 450

Location

Germany

Related Subject Headings

  • TRPV Cation Channels
  • Pharmacology & Pharmacy
  • Pain
  • Joints
  • Joint Diseases
  • Humans
  • Cartilage
  • Bone and Bones
  • Animals
  • 3214 Pharmacology and pharmaceutical sciences
 

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McNulty, A. L., Leddy, H. A., Liedtke, W., & Guilak, F. (2015). TRPV4 as a therapeutic target for joint diseases. Naunyn Schmiedebergs Arch Pharmacol, 388(4), 437–450. https://doi.org/10.1007/s00210-014-1078-x
McNulty, Amy L., Holly A. Leddy, Wolfgang Liedtke, and Farshid Guilak. “TRPV4 as a therapeutic target for joint diseases.Naunyn Schmiedebergs Arch Pharmacol 388, no. 4 (April 2015): 437–50. https://doi.org/10.1007/s00210-014-1078-x.
McNulty AL, Leddy HA, Liedtke W, Guilak F. TRPV4 as a therapeutic target for joint diseases. Naunyn Schmiedebergs Arch Pharmacol. 2015 Apr;388(4):437–50.
McNulty, Amy L., et al. “TRPV4 as a therapeutic target for joint diseases.Naunyn Schmiedebergs Arch Pharmacol, vol. 388, no. 4, Apr. 2015, pp. 437–50. Pubmed, doi:10.1007/s00210-014-1078-x.
McNulty AL, Leddy HA, Liedtke W, Guilak F. TRPV4 as a therapeutic target for joint diseases. Naunyn Schmiedebergs Arch Pharmacol. 2015 Apr;388(4):437–450.
Journal cover image

Published In

Naunyn Schmiedebergs Arch Pharmacol

DOI

EISSN

1432-1912

Publication Date

April 2015

Volume

388

Issue

4

Start / End Page

437 / 450

Location

Germany

Related Subject Headings

  • TRPV Cation Channels
  • Pharmacology & Pharmacy
  • Pain
  • Joints
  • Joint Diseases
  • Humans
  • Cartilage
  • Bone and Bones
  • Animals
  • 3214 Pharmacology and pharmaceutical sciences