Ca2+-independent but voltage-dependent quantal catecholamine secretion (CiVDS) in the mammalian sympathetic nervous system

Author:

Huang Rong,Wang Yuan,Li Jie,Jiang Xiaohan,Li Yinglin,Liu Bing,Wu Xi,Du Xingyu,Hang Yuqi,Jin Mu,Zhu Feipeng,Wang ChangheORCID,Chai Zuying,Zhou Zhuan

Abstract

Action potential-induced vesicular exocytosis is considered exclusively Ca2+dependent in Katz’s Ca2+hypothesis on synaptic transmission. This long-standing concept gets an exception following the discovery of Ca2+-independent but voltage-dependent secretion (CiVDS) and its molecular mechanisms in dorsal root ganglion sensory neurons. However, whether CiVDS presents only in sensory cells remains elusive. Here, by combining multiple independent recordings, we report that [1] CiVDS robustly presents in the sympathetic nervous system, including sympathetic superior cervical ganglion neurons and slice adrenal chromaffin cells, [2] uses voltage sensors of Ca2+channels (N-type and novel L-type), and [3] contributes to catecholamine release in both homeostatic and fight-or-flight like states; [4] CiVDS-mediated catecholamine release is faster than that of Ca2+-dependent secretion at the quantal level and [5] increases Ca2+currents and contractility of cardiac myocytes. Together, CiVDS presents in the sympathetic nervous system with potential physiological functions, including cardiac muscle contractility.

Funder

National Natural Science Foundation of China

NATIONAL KEY RESEARCH AND DEVELOPMENT PROGRAM OF CHIAN

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference75 articles.

1. B. Katz , “Nobel lecture: On the quantal mechanism of neural transmitter release” in Nobel Lectures, Physiology or Medicine 1963-1970 (Elsevier, Amsterdam, 1972).

2. Ion channels for communication between and within cells

3. The Molecular Machinery of Neurotransmitter Release (Nobel Lecture)

4. Calcium Control of Neurotransmitter Release

5. Synaptotagmin: A Ca2+ sensor that triggers exocytosis?

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