Fagan Amy, Sponchiado Mariana, Mata Luz, Amin Shanil, Aguirre J Ignacio, Prabhakaran Sreekala, Reznikov Leah R
Department of Physiological Sciences, University of Florida, Gainesville, FL, United States.
Department of Pediatrics, Pediatric Pulmonary Division, University of Florida, Gainesville, FL, United States.
Front Physiol. 2025 Jun 23;16:1578553. doi: 10.3389/fphys.2025.1578553. eCollection 2025.
Brain-derived neurotrophic factor (BDNF) is a neural plasticity molecule that is increasingly recognized for its role in airway pathophysiology, including diseases like asthma. Although many cells in the airway can produce BDNF, our understanding of epithelial-derived BDNF and its role in airway health and disease remains limited.
In the current study, we studied male and female mice with conditional loss of Bdnf in airway club cells and challenged them intranasally with saline (vehicle control) or interleukin 13 (IL-13) for 4 days. We measured pulmonary mechanics and the abundance and secretion characteristics of the major secreted mucin glycoproteins, mucin 5B () and mucin 5ac ().
Female mice with conditional loss of club cell showed increased Muc5b protein in the airway epithelia under basal and IL-13-stimulated conditions compared to female mice with intact . In contrast, conditional loss of club cell Bdnf in male mice augmented whole-lung mRNA levels under basal and IL-13-stimulated conditions. IL-13-treated female mice with conditional loss of club cell Bdnf showed decreased airway elastance in response to increasing concentrations of nebulized methacholine, suggesting that loss of club cell had a protective effect. No statistically significant differences were observed in pulmonary mechanics between male mice with or without conditional loss of epithelial cell , although treatment effects of IL-13 were noted. Mechanistic and complementary studies performed in NCI-H322 cells, a human cell line with "club cell-like" characteristics, failed to demonstrate a relationship among BDNF, IL-13 signaling, and at the mRNA level.
These data highlight sex-dependent differences and club cell-specific effects of in regulating airway physiology under inflammatory conditions in mice, suggesting that further studies are needed to understand potential translational implications.
脑源性神经营养因子(BDNF)是一种神经可塑性分子,其在气道病理生理学(包括哮喘等疾病)中的作用日益受到认可。尽管气道中的许多细胞都能产生BDNF,但我们对上皮来源的BDNF及其在气道健康和疾病中的作用的了解仍然有限。
在本研究中,我们对气道俱乐部细胞中条件性缺失Bdnf的雄性和雌性小鼠进行了研究,并通过鼻腔给予它们生理盐水(载体对照)或白细胞介素13(IL-13),持续4天。我们测量了肺力学以及主要分泌性粘蛋白糖蛋白、粘蛋白5B(Muc5b)和粘蛋白5AC(Muc5ac)的丰度和分泌特性。
与Bdnf完整的雌性小鼠相比,气道俱乐部细胞条件性缺失Bdnf的雌性小鼠在基础和IL-13刺激条件下,气道上皮中的Muc5b蛋白增加。相反,在基础和IL-13刺激条件下,雄性小鼠气道俱乐部细胞Bdnf的条件性缺失增加了全肺Muc5ac mRNA水平。经IL-13处理的气道俱乐部细胞Bdnf条件性缺失的雌性小鼠,随着雾化乙酰甲胆碱浓度的增加,气道弹性降低,这表明俱乐部细胞Bdnf的缺失具有保护作用。尽管注意到了IL-13的治疗效果,但在有或没有上皮细胞Bdnf条件性缺失的雄性小鼠之间,肺力学方面未观察到统计学上的显著差异。在具有“俱乐部细胞样”特征的人细胞系NCI-H322细胞中进行的机制和补充研究未能在mRNA水平上证明BDNF、IL-13信号传导和Muc5ac之间的关系。
这些数据突出了Bdnf在调节小鼠炎症条件下气道生理方面的性别依赖性差异和俱乐部细胞特异性作用,表明需要进一步研究以了解潜在的转化意义。