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

• Published in: International journal of molecular medicine Vol. 41; no. 3; pp. 1213 - 1223
• Main Authors: Schrenk, Sandra, Cenzi, Carola, Bertalot, Thomas, Conconi, Maria Teresa, Di Liddo, Rosa
• Format: Journal Article
• Language: English
• Published: Greece Spandidos Publications 01.03.2018; Spandidos Publications UK Ltd
• Subjects: Binding sites; Collagen; Disease susceptibility; Epidermal growth factor; Gene mutation; Genetic aspects; Genotype & phenotype; Glycoproteins; Health aspects; Homeostasis; Inflammation; Inflammatory bowel disease; Proteins
• ISSN: 1107-3756; 1791-244X
• DOI: 10.3892/ijmm.2017.3343

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.