Evidence map›Paper›PMID 24266713›Full record

ArticleJournal of neurochemistry2014

Chromogranin B: intra- and extra-cellular mechanisms to regulate catecholamine storage and release, in catecholaminergic cells and organisms.

Kuixing Zhang, Nilima Biswas, Jiaur R Gayen, Jose Pablo Miramontes-Gonzalez, C Makena Hightower, Maja Mustapic, Manjula Mahata, Chun-Teng Huang, Vivian Y Hook, Sushil K Mahata and 2 more

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 22 citations in OpenAlex.

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  11. NRSF: an angel or a devil in neurogenesis and neurological diseases.Journal of molecular neuroscience : MN · 2015
    Review
  12. Article
  13. The granin VGF promotes genesis of secretory vesicles, and regulates circulating catecholamine levels and blood pressure.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Kuixing ZhangDepartments of Medicine and Pharmacology, and Institute for Genomic Medicine (IGM), University of California at San Diego, La Jolla, California, USA; VA San Diego Healthcare System, La Jolla, California, USA.
Nilima Biswas
Jiaur R Gayen
Jose Pablo Miramontes-Gonzalez
C Makena Hightower
Maja Mustapic
Manjula Mahata
Chun-Teng Huang
Vivian Y Hook
Sushil K Mahata
Sucheta Vaingankar
Daniel T O'Connor
VA San Diego Healthcare System · USUniversity of California, San Diego · US

Funding

Trafficking of catecholamine storage vesicle proteinsP01HL058120 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI O'CONNOR, DANIEL T · 1999 to 2009
$18.5M
Homeostatic regulation of autonomic physiology by chromogranin AR01HL108629 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VAINGANKAR, SUCHETA M · 2012 to 2015
$1.5M
Hypertensive kidney disease: Novel pathogenic and therapeutic pathwayR01DK094894 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VAINGANKAR, SUCHETA M · 2012 to 2015
$1.4M
Sympathetic Outflow to Catecholamine Storage VesiclesR01DK060702 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI O'CONNOR, DANIEL T · 2002 to 2006
$1.4M
NHLBI NIH HHS P01 HL058120NHLBI NIH HHS R01 HL108629NIDDK NIH HHS R01 DK060702NIDDK NIH HHS R01 DK094894
6 · The paper itself

Abstract

Chromogranin B (CHGB) is the major matrix protein in human catecholamine storage vesicles. CHGB genetic variation alters catecholamine secretion and blood pressure. Here, effective Chgb protein under-expression was achieved by siRNA in PC12 cells, resulting in ~ 48% fewer secretory granules on electron microscopy, diminished capacity for catecholamine uptake (by ~ 79%), and a ~ 73% decline in stores available for nicotinic cholinergic-stimulated secretion. In vivo, loss of Chgb in knockout mice resulted in a ~ 35% decline in chromaffin granule abundance and ~ 44% decline in granule diameter, accompanied by unregulated catecholamine release into plasma. Over-expression of CHGB was achieved by transduction of a CHGB-expressing lentivirus, resulting in ~ 127% elevation in CHGB protein, with ~ 122% greater abundance of secretory granules, but only ~ 14% increased uptake of catecholamines, and no effect on nicotinic-triggered secretion. Human CHGB protein and its proteolytic fragments inhibited nicotinic-stimulated catecholamine release by ~ 72%. One conserved-region CHGB peptide inhibited nicotinic-triggered secretion by up to ~ 41%, with partial blockade of cationic signal transduction. We conclude that bi-directional quantitative derangements in CHGB abundance result in profound changes in vesicular storage and release of catecholamines. When processed and released extra-cellularly, CHGB proteolytic fragments exert a feedback effect to inhibit catecholamine secretion, especially during nicotinic cholinergic stimulation.

Indexed as

Amino Acid SequenceAnimalsCatecholaminesChromaffin GranulesChromogranin BExtracellular FluidHumansIntracellular FluidMiceMice, KnockoutMolecular Sequence DataRatsCatecholaminesChromogranin Bchromogranin B, ratadrenalcatecholamineschromaffinchromogranin Bhypertension

Identifiers

PMID24266713
PMCPMC3992281
OpenAlexW2041201675

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.