Structural and functional failure of fibrillin‑1 in human diseases (Review)

Int J Mol Med. 2018 Mar;41(3):1213-1223. doi: 10.3892/ijmm.2017.3343. Epub 2017 Dec 22.

Abstract

Fibrillins (FBNs) are key relay molecules that form the backbone of microfibrils in elastic and non‑elastic tissues. Interacting with other components of the extracellular matrix (ECM), these ubiquitous glycoproteins exert pivotal roles in tissue development, homeostasis and repair. In addition to mechanical support, FBN networks also exhibit regulatory activities on growth factor signalling, ECM formation, cell behaviour and the immune response. Consequently, mutations affecting the structure, assembly and stability of FBN microfibrils have been associated with impaired biomechanical tissue properties, altered cell‑matrix interactions, uncontrolled growth factor or cytokine activation, and the development of fibrillinopathies and associated severe complications in multiple organs. Beyond a panoramic overview of structural cues of the FBN network, the present review will also describe the pathological implications of FBN disorders in the development of inflammatory and fibrotic conditions.

Publication types

  • Review

MeSH terms

  • Animals
  • Disease*
  • Elastin / metabolism
  • Extracellular Matrix / metabolism
  • Fibrillin-1 / chemistry*
  • Fibrillin-1 / metabolism*
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Signal Transduction

Substances

  • Fibrillin-1
  • Intercellular Signaling Peptides and Proteins
  • Elastin