i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
ICBAS-Instuto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, 4030-313 Porto, Portugal.
Biomolecules. 2023 Feb 24;13(3):425. doi: 10.3390/biom13030425.
Cystic fibrosis is a monogenic disease with a multisystemic phenotype, ranging from predisposition to chronic lung infection and inflammation to reduced bone mass. The exact mechanisms unbalancing the maintenance of an optimal bone mass in cystic fibrosis patients remain unknown. Multiple factors may contribute to severe bone mass reduction that, in turn, have devastating consequences in the patients' quality of life and longevity. Here, we will review the existing evidence linking the CFTR dysfunction and cell-intrinsic bone defects. Additionally, we will also address how the proinflammatory environment due to CFTR dysfunction in immune cells and chronic infection impairs the maintenance of an adequate bone mass in CF patients.
囊性纤维化是一种单基因疾病,具有多系统表型,从易患慢性肺部感染和炎症到骨量减少不等。导致囊性纤维化患者骨量维持失衡的确切机制尚不清楚。多种因素可能导致严重的骨量减少,进而对患者的生活质量和寿命产生毁灭性的影响。在这里,我们将回顾现有的证据,将 CFTR 功能障碍与细胞内骨缺陷联系起来。此外,我们还将讨论由于免疫细胞中 CFTR 功能障碍和慢性感染导致的促炎环境如何损害 CF 患者维持足够骨量的能力。