scholarly journals Chromogranin A, the Major Lumenal Protein in Chromaffin Granules, Controls Fusion Pore Expansion

2019 ◽  
Vol 116 (3) ◽  
pp. 524a ◽  
Author(s):  
Prabhodh S. Abbineni ◽  
Mary A. Bittner ◽  
Daniel Axelrod ◽  
Ronald W. Holz
2018 ◽  
Vol 151 (2) ◽  
pp. 118-130 ◽  
Author(s):  
Prabhodh S. Abbineni ◽  
Mary A. Bittner ◽  
Daniel Axelrod ◽  
Ronald W. Holz

Upon fusion of the secretory granule with the plasma membrane, small molecules are discharged through the immediately formed narrow fusion pore, but protein discharge awaits pore expansion. Recently, fusion pore expansion was found to be regulated by tissue plasminogen activator (tPA), a protein present within the lumen of chromaffin granules in a subpopulation of chromaffin cells. Here, we further examined the influence of other lumenal proteins on fusion pore expansion, especially chromogranin A (CgA), the major and ubiquitous lumenal protein in chromaffin granules. Polarized TIRF microscopy demonstrated that the fusion pore curvature of granules containing CgA-EGFP was long lived, with curvature lifetimes comparable to those of tPA-EGFP–containing granules. This was surprising because fusion pore curvature durations of granules containing exogenous neuropeptide Y-EGFP (NPY-EGFP) are significantly shorter (80% lasting <1 s) than those containing CgA-EGFP, despite the anticipated expression of endogenous CgA. However, quantitative immunocytochemistry revealed that transiently expressed lumenal proteins, including NPY-EGFP, caused a down-regulation of endogenously expressed proteins, including CgA. Fusion pore curvature durations in nontransfected cells were significantly longer than those of granules containing overexpressed NPY but shorter than those associated with granules containing overexpressed tPA, CgA, or chromogranin B. Introduction of CgA to NPY-EGFP granules by coexpression converted the fusion pore from being transient to being longer lived, comparable to that found in nontransfected cells. These findings demonstrate that several endogenous chromaffin granule lumenal proteins are regulators of fusion pore expansion and that alteration of chromaffin granule contents affects fusion pore lifetimes. Importantly, the results indicate a new role for CgA. In addition to functioning as a prohormone, CgA plays an important role in controlling fusion pore expansion.


2014 ◽  
Vol 107 (1) ◽  
pp. 26-33 ◽  
Author(s):  
Annita Ngatchou Weiss ◽  
Arun Anantharam ◽  
Mary A. Bittner ◽  
Daniel Axelrod ◽  
Ronald W. Holz

1996 ◽  
Vol 271 (45) ◽  
pp. 28533-28540 ◽  
Author(s):  
Jean-Marc Strub ◽  
Yannick Goumon ◽  
Karine Lugardon ◽  
Calliope Capon ◽  
Michel Lopez ◽  
...  

1990 ◽  
Vol 138 (4) ◽  
pp. 565-574 ◽  
Author(s):  
K. B. HELLE ◽  
R. K. REED ◽  
M. EHRHART ◽  
D. AUNIS ◽  
R. HOGUE ANGELETTI

2019 ◽  
Vol 699 ◽  
pp. 134-139 ◽  
Author(s):  
Prabhodh S. Abbineni ◽  
Kevin P. Bohannon ◽  
Mary A. Bittner ◽  
Daniel Axelrod ◽  
Ronald W. Holz

2017 ◽  
Vol 149 (10) ◽  
pp. 893-896
Author(s):  
Meyer B. Jackson

Slow fusion pore expansion could retain molecules within vesicles, enabling a chemical reaction that modifies secreted products.


2014 ◽  
Vol 306 (9) ◽  
pp. C831-C843 ◽  
Author(s):  
Prattana Samasilp ◽  
Kyle Lopin ◽  
Shyue-An Chan ◽  
Rajesh Ramachandran ◽  
Corey Smith

Adrenal neuroendocrine chromaffin cells receive excitatory synaptic input from the sympathetic nervous system and secrete hormones into the peripheral circulation. Under basal sympathetic tone, modest amounts of freely soluble catecholamine are selectively released through a restricted fusion pore formed between the secretory granule and the plasma membrane. Upon activation of the sympathoadrenal stress reflex, elevated stimulation drives fusion pore expansion, resulting in increased catecholamine secretion and facilitating release of copackaged peptide hormones. Thus regulated expansion of the secretory fusion pore is a control point for differential hormone release of the sympathoadrenal stress response. Previous work has shown that syndapin 1 deletion alters transmitter release and that the dynamin 1-syndapin 1 interaction is necessary for coupled endocytosis in neurons. Dynamin has also been shown to be involved in regulation of fusion pore expansion in neuroendocrine chromaffin cells through an activity-dependent association with syndapin. However, it is not known which syndapin isoform(s) contributes to pore dynamics in neuroendocrine cells. Nor is it known at what stage of the secretion process dynamin and syndapin associate to modulate pore expansion. Here we investigate the expression and localization of syndapin isoforms and determine which are involved in mediating fusion pore expansion. We show that all syndapin isoforms are expressed in the adrenal medulla. Mutation of the SH3 dynamin-binding domain of all syndapin isoforms shows that fusion pore expansion and catecholamine release are limited specifically by mutation of syndapin 3. The mutation also disrupts targeting of syndapin 3 to the cell periphery. Syndapin 3 exists in a persistent colocalized state with dynamin 1.


FEBS Letters ◽  
1988 ◽  
Vol 231 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Thomas Wohlfarter ◽  
Reiner Fischer-Colbrie ◽  
Ruth Hogue-Angeletti ◽  
Lee E. Eiden ◽  
Hans Winkler

2015 ◽  
Vol 8 (2) ◽  
pp. e1018496 ◽  
Author(s):  
Kathrin Neuland ◽  
Manfred Frick
Keyword(s):  

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