胶质细胞源性神经生长因子
神经营养因子
细胞生物学
GDNF配体家族
内质网
生物
免疫学
化学
内科学
医学
受体
作者
Li Y. Drake,B. Roos,J.J. Teske,Niyati A. Borkar,Savita Ayyalasomayajula,Courtney Klapperich,Maunick Lefin Koloko Ngassie,Christina M. Pabelick,Y. S. Prakash
出处
期刊:American Journal of Physiology-lung Cellular and Molecular Physiology
[American Physiological Society]
日期:2024-09-24
标识
DOI:10.1152/ajplung.00101.2024
摘要
Airway smooth muscle (ASM) cells play important roles in airway remodeling of asthma. Our previous studies show that in vivo administration of glial derived neurotrophic factor (GDNF) in mice induces thickening and collagen deposition in bronchial airways, while chelation of GDNF by GFRα1-Fc attenuates airway remodeling in the context of allergen exposure. To determine whether GDNF has direct effects on ASM, in this study, we examined GDNF in ASM cells from normal vs. asthmatic humans. We found that GDNF treatment of human ASM cells had only minor effects on cell proliferation, intracellular expression or extracellular deposition of collagen I, collagen III, and fibronectin. Endoplasmic reticulum (ER) stress response and mitochondrial function have been implicated in asthma. We investigated whether GDNF regulates these aspects in human ASM. We found that GDNF treatment did not affect ER stress protein expression in normal or asthmatic cells. However, GDNF treatment impaired mitochondrial morphology in ASM but without significant effects on mitochondrial respiration. Thus, it is likely that in vivo effects of GDNF on airway remodeling per se involve cell types other than those on ASM, and thus ASM may serve more as a source of GDNF rather than a target.
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