Human airway smooth muscle cell proliferation from asthmatics is negatively regulated by semaphorin3A

Oncotarget. 2016 Dec 6;7(49):80238-80251. doi: 10.18632/oncotarget.12884.

Abstract

Airway smooth muscle (ASM) hyperplasia is a key feature of airway remodeling in development of lung diseases such as asthma. Anomalous proliferation of ASM cells directly contributes to ASM hyperplasia. However, the molecular mechanisms controlling ASM cell proliferation are not completely understood. Semaphorins are versatile regulators of various cellular processes including cell growth and proliferation. The role of semaphorins in ASM cell proliferation has remained to be addressed. Here, we report that semaphorin 3A (Sema3A) receptor, neuropilin 1 (Nrp1), is expressed on human ASM cells (HASMC) isolated from healthy and asthmatic donors and treatment of these cells with exogenous Sema3A inhibits growth factor-induced proliferation. Sema3A inhibitory effect on HASMC proliferation is associated with decreased tyrosine phosphorylation of PDGFR, downregulation of Rac1 activation, STAT3 and GSK-3β phosphorylation. Bronchial sections from severe asthmatics displayed immunoreactivity of Nrp1, suggestive of functional contribution of Sema3A-Nrp1 axis in airway remodeling. Together, our data suggest Sema3A-Nrp1 signaling as a novel regulatory pathway of ASM hyperplasia.

Keywords: Pathology Section; airway remodeling; asthma; neuropilin 1; platelet-derived growth factor; semaphorin 3A.

MeSH terms

  • Adult
  • Airway Remodeling*
  • Asthma / genetics
  • Asthma / metabolism*
  • Asthma / pathology
  • Asthma / physiopathology
  • Bronchi / metabolism*
  • Bronchi / pathology
  • Bronchi / physiopathology
  • Case-Control Studies
  • Cell Line
  • Cell Proliferation*
  • Female
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Humans
  • Hyperplasia
  • Male
  • Muscle, Smooth / metabolism*
  • Muscle, Smooth / pathology
  • Muscle, Smooth / physiopathology
  • Myocytes, Smooth Muscle / metabolism*
  • Myocytes, Smooth Muscle / pathology
  • Neuropilin-1 / genetics
  • Neuropilin-1 / metabolism
  • Phosphorylation
  • Receptors, Platelet-Derived Growth Factor / metabolism
  • STAT3 Transcription Factor / metabolism
  • Semaphorin-3A / metabolism*
  • Signal Transduction
  • Time Factors
  • Young Adult
  • rac1 GTP-Binding Protein / metabolism

Substances

  • RAC1 protein, human
  • SEMA3A protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Semaphorin-3A
  • Neuropilin-1
  • Receptors, Platelet-Derived Growth Factor
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • rac1 GTP-Binding Protein