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肺神经内分泌细胞:呼吸功能和气道-神经通讯的关键参与者。

Pulmonary neuroendocrine cells: crucial players in respiratory function and airway-nerve communication.

作者信息

Thakur Abhimanyu, Mei Shuya, Zhang Noel, Zhang Kui, Taslakjian Boghos, Lian Jiacee, Wu Shuang, Chen Bohao, Solway Julian, Chen Huanhuan Joyce

机构信息

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.

Ben May Department for Cancer Research, The University of Chicago, Chicago, IL, United States.

出版信息

Front Neurosci. 2024 Aug 8;18:1438188. doi: 10.3389/fnins.2024.1438188. eCollection 2024.

Abstract

Pulmonary neuroendocrine cells (PNECs) are unique airway epithelial cells that blend neuronal and endocrine functions, acting as key sensors in the lung. They respond to environmental stimuli like allergens by releasing neuropeptides and neurotransmitters. PNECs stand out as the only lung epithelial cells innervated by neurons, suggesting a significant role in airway-nerve communication via direct neural pathways and hormone release. Pathological conditions such as asthma are linked to increased PNECs counts and elevated calcitonin gene-related peptide (CGRP) production, which may affect neuroprotection and brain function. CGRP is also associated with neurodegenerative diseases, including Parkinson's and Alzheimer's, potentially due to its influence on inflammation and cholinergic activity. Despite their low numbers, PNECs are crucial for a wide range of functions, highlighting the importance of further research. Advances in technology for producing and culturing human PNECs enable the exploration of new mechanisms and cell-specific responses to targeted therapies for PNEC-focused treatments.

摘要

肺神经内分泌细胞(PNECs)是独特的气道上皮细胞,兼具神经元和内分泌功能,是肺部的关键传感器。它们通过释放神经肽和神经递质对过敏原等环境刺激作出反应。PNECs是唯一受神经元支配的肺上皮细胞,这表明其在通过直接神经通路和激素释放进行气道-神经通讯中发挥着重要作用。哮喘等病理状况与PNECs数量增加和降钙素基因相关肽(CGRP)产生增加有关,这可能会影响神经保护和脑功能。CGRP还与包括帕金森病和阿尔茨海默病在内的神经退行性疾病有关,这可能是由于其对炎症和胆碱能活性的影响。尽管PNECs数量较少,但它们对多种功能至关重要,凸显了进一步研究的重要性。用于生产和培养人PNECs的技术进步,使得探索针对以PNECs为重点治疗的新机制和细胞特异性反应成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef26/11340541/7606c046ce17/fnins-18-1438188-g001.jpg

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