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Am J Physiol Lung Cell Mol Physiol (April 28, 2006). doi:10.1152/ajplung.00501.2005
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Submitted on November 26, 2005
Accepted on March 21, 2006

NEUROTROPHIN EFFECTS ON INTRACELLULAR Ca2+ AND FORCE IN AIRWAY SMOOTH MUSCLE

Y.S. Prakash1*, Adeyemi Iyanoye2, Binnaz Ay3, Carlos B. Mantilla1, and Christina M Pabelick4

1 Department of Anesthesiology, Mayo Clinic College of Medicine, Rochester, Minnesota, United States; Department of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine, Rochester, Minnesota, United States
2 Department of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine, Rochester, Minnesota, United States
3 Department of Anesthesiology, Marmara University, Istanbul, Turkey
4 Department of Anesthesiology, Mayo Clinic College of Medicine, Rochester, Minnesota, United States

* To whom correspondence should be addressed. E-mail: prakash.ys{at}mayo.edu.

Neurotrophins (e.g. brain derived neurotrophic factor (BDNF), neurotrophin 4 (NT4)) known to affect neuronal structure and function, are expressed in non-neuronal tissues including the airway. However, their function is unclear. We examined the effect of acute vs. prolonged neurotrophin exposure on regulation of airway smooth muscle (ASM) intracellular Ca2+ ([Ca2+]i): sarcoplasmic reticulum (SR) Ca2+ release and Ca2+ influx (specifically store-operated Ca2+ entry; SOCE). Human ASM cells were incubated for 30 min in medium (control) or 1 or 10 nM BDNF, NT3 or NT4 (acute exposure) or overnight in 1 nM BDNF, NT3 or NT4 (prolonged exposure), and imaged after loading with the Ca2+ indicator fura-2/AM. [Ca2+]i responses to ACh, histamine, bradykinin and caffeine, and SOCE following SR Ca2+ depletion were compared across cell groups. Force measurements were performed in human bronchial strips exposed to NTs. Basal [Ca2+]i, peak responses to all agonists, SOCE, and force responses to ACh and histamine, were all significantly enhanced by both acute and prolonged BDNF exposure (smaller effect of NT4), but decreased by NT3. Inhibition of the BDNF/NT4 receptor trkB by K252a prevented enhancement of [Ca2+]i responses. ASM cells showed positive immunostaining for BDNF, NT3, NT4,trkB and trkC (NT3 receptor). These novel data demonstrate that neurotrophins influence ASM [Ca2+]i and force regulation, and suggest a potential role for neurotrophins in airway diseases.




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