Wellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK; Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Semin Cell Dev Biol. 2019 May;89:109-117. doi: 10.1016/j.semcdb.2018.07.016. Epub 2018 Jul 20.
Fibrillin microfibrils are extensible polymers that endow connective tissues with long-range elasticity and have widespread distributions in both elastic and non-elastic tissues. They act as a template for elastin deposition during elastic fibre formation and are essential for maintaining the integrity of tissues such as blood vessels, lung, skin and ocular ligaments. A reduction in fibrillin is seen in tissues in vascular ageing, chronic obstructive pulmonary disease, skin ageing and UV induced skin damage, and age-related vision deterioration. Most mutations in fibrillin cause Marfan syndrome, a genetic disease characterised by overgrowth of the long bones and other skeletal abnormalities with cardiovascular and eye defects. However, mutations in fibrillin and fibrillin-binding proteins can also cause short-stature pathologies. All of these diseases have been linked to dysregulated growth factor signalling which forms a major functional role for fibrillin.
原纤维微纤维是可伸展的聚合物,为结缔组织提供长程弹性,并在弹性组织和非弹性组织中广泛分布。它们在弹性纤维形成过程中充当弹性蛋白沉积的模板,对于维持血管、肺、皮肤和眼韧带等组织的完整性至关重要。在血管老化、慢性阻塞性肺病、皮肤老化和紫外线引起的皮肤损伤以及与年龄相关的视力恶化等组织中,原纤维的减少可见。原纤维中的大多数突变导致马凡综合征,这是一种遗传疾病,其特征是长骨和其他骨骼异常过度生长,伴有心血管和眼部缺陷。然而,原纤维和原纤维结合蛋白的突变也可导致身材矮小的病理。所有这些疾病都与失调的生长因子信号有关,这是原纤维的主要功能作用。