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editorial
. 2016 May 15;193(10):1075–1077. doi: 10.1164/rccm.201512-2454ED

Figure 1.

Figure 1.

Effects of cystic fibrosis transmembrane conductance regulator (CFTR) defect on integrin activation. Absence or mutations in CFTR cause reduced Ras homolog gene family member A (RhoA) and cell division control protein 42 (Cdc42) activation, resulting in impaired α4 and β2 integrin activation and monocyte function. CF = cystic fibrosis.