Signaling Pathways Regulating Cartilage Formation

  • Faiza Ramzan
  • , Asmat Salim
  • , Irfan Khan

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

3 Citations (Scopus)

Abstract

Over the course of many years of investigation, the molecular processes that regulate the differentiation of chondrocytes throughout the development of carti-lage from their initial activation from mesenchymal progenitor cells to their eventual maturation into hypertrophic chondrocytes have been discovered. In this chapter, we take a glance at the interaction between a number of signaling molecules, mechanical cues, and morphological cell characteristics to activate a specific subset of crucial transcription factors that regulate the genetic program that triggers chondrogenesis and chondrocyte divergence, which leads to the formation of cartilage. We also discuss current research on how various signal transduction pathways regulate chondrocyte differentiation and multiplication in the articular surface. In adult normal cartilage, the anabolic and catabolic pro-cesses of chondrocyte maturation are delicately balanced. Due to the degradation of joint with age, the body’s ability to maintain homeostasis is compromised, catabolic pathways are triggered, and cartilage is acutely and severely prone to degeneration. Because the differentiation of cartilage and maintenance of cellular metabolism are intricately governed by a complex series of signal transduction and biophysical elements of the system, it appears that recognizing these pro-cesses will be beneficial for both exploring the molecular and biological methods for cartilage tissue engineering and identification of the disease-causing major elements for particular therapeutics for management of the disease progression. This chapter will emphasize on the key signaling pathways that can activate the cellular, subcellular, and biochemical mechanisms, controlling functional properties of the cartilage under normal circumstances. These pathways may have an impact on how various cartilage tissue compartments interact. Consequently, the study in this area may result in the development of more efficient cartilage regeneration therapies.

Original languageEnglish (UK)
Title of host publicationCartilage
Subtitle of host publicationFrom Biology to Biofabrication
PublisherSpringer Nature
Pages125-154
Number of pages30
ISBN (Electronic)9789819924523
ISBN (Print)9789819924516
DOIs
Publication statusPublished - 1 Jan 2023
Externally publishedYes

Keywords

  • BMP
  • Cartilage signaling pathways
  • Chondrocytes
  • FGF
  • GDF-5
  • Hedgehog signaling
  • IGF-1
  • Notch signaling

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