دورية أكاديمية

ATP Release Channels

التفاصيل البيبلوغرافية
العنوان: ATP Release Channels
المؤلفون: Akiyuki Taruno
المصدر: International Journal of Molecular Sciences, Vol 19, Iss 3, p 808 (2018)
بيانات النشر: MDPI AG, 2018.
سنة النشر: 2018
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: ATP, purinergic signaling, ion channel, connexin, pannexin, CALHM, VRAC, VSOR, maxi-anion channel, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: Adenosine triphosphate (ATP) has been well established as an important extracellular ligand of autocrine signaling, intercellular communication, and neurotransmission with numerous physiological and pathophysiological roles. In addition to the classical exocytosis, non-vesicular mechanisms of cellular ATP release have been demonstrated in many cell types. Although large and negatively charged ATP molecules cannot diffuse across the lipid bilayer of the plasma membrane, conductive ATP release from the cytosol into the extracellular space is possible through ATP-permeable channels. Such channels must possess two minimum qualifications for ATP permeation: anion permeability and a large ion-conducting pore. Currently, five groups of channels are acknowledged as ATP-release channels: connexin hemichannels, pannexin 1, calcium homeostasis modulator 1 (CALHM1), volume-regulated anion channels (VRACs, also known as volume-sensitive outwardly rectifying (VSOR) anion channels), and maxi-anion channels (MACs). Recently, major breakthroughs have been made in the field by molecular identification of CALHM1 as the action potential-dependent ATP-release channel in taste bud cells, LRRC8s as components of VRACs, and SLCO2A1 as a core subunit of MACs. Here, the function and physiological roles of these five groups of ATP-release channels are summarized, along with a discussion on the future implications of understanding these channels.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1422-0067
Relation: http://www.mdpi.com/1422-0067/19/3/808; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms19030808
URL الوصول: https://doaj.org/article/bf2327ac3ef14aa68efbe0254c5c30fd
رقم الأكسشن: edsdoj.bf2327ac3ef14aa68efbe0254c5c30fd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14220067
DOI:10.3390/ijms19030808