Evidence map›Paper›PMID 25915053›Full record

ArticlePloS one2015

Transcription Factor CREB3L1 Regulates Endoplasmic Reticulum Stress Response Genes in the Osmotically Challenged Rat Hypothalamus.

Mingkwan Greenwood, Michael Paul Greenwood, Julian F R Paton, David Murphy

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  4. Review
  5. Osmosensitive transcription factors in the prolactin cell of a euryhaline teleost.Comparative biochemistry and physiology. Part A, Molecular & integrative physiology · 2023
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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

4 authors at 2 institutions in 2 countries.

Mingkwan GreenwoodSchool of Clinical Sciences, University of Bristol, Bristol, England.
Michael Paul GreenwoodSchool of Clinical Sciences, University of Bristol, Bristol, England.
Julian F R PatonSchool of Physiology and Pharmacology, University of Bristol, Bristol, England.
David MurphySchool of Clinical Sciences, University of Bristol, Bristol, England; Department of Physiology, University of Malaya, Kuala Lumpur, Malaysia.
University of Bristol · GBUniversity of Malaya · MY

Funding

Biotechnology and Biological Sciences Research Council BB/G006156/1Biotechnology and Biological Sciences Research Council BB/J015415/1British Heart Foundation RG/12/6/29670
6 · The paper itself

Abstract

Arginine vasopressin (AVP) is synthesised in magnocellular neurons (MCNs) of supraoptic nucleus (SON) and paraventricular nucleus (PVN) of the hypothalamus. In response to the hyperosmotic stressors of dehydration (complete fluid deprivation, DH) or salt loading (drinking 2% salt solution, SL), AVP synthesis increases in MCNs, which over-burdens the protein folding machinery in the endoplasmic reticulum (ER). ER stress and the unfolded protein response (UPR) are signaling pathways that improve ER function in response to the accumulation of misfold/unfold protein. We asked whether an ER stress response was activated in the SON and PVN of DH and SL rats. We observed increased mRNA expression for the immunoglobulin heavy chain binding protein (BiP), activating transcription factor 4 (Atf4), C/EBP-homologous protein (Chop), and cAMP responsive element binding protein 3 like 1 (Creb3l1) in both SON and PVN of DH and SL rats. Although we found no changes in the splicing pattern of X box-binding protein 1 (Xbp1), an increase in the level of the unspliced form of Xbp1 (Xbp1U) was observed in DH and SL rats. CREB3L1, a novel ER stress inducer, has been shown to be activated by ER stress to regulate the expression of target genes. We have previously shown that CREB3L1 is a transcriptional regulator of the AVP gene; however, a role for CREB3L1 in the response to ER stress has yet to be investigated in MCNs. Here, we used lentiviral vectors to introduce a dominant negative form of CREB3L1 (CREB3L1DN) in the rat SON. Expression of CREB3L1DN in the SON decreased Chop and Xbp1U mRNA levels, but not BiP and Atf4 transcript expression. CREB3L1 is thus implicated as a transcriptional mediator of the ER stress response in the osmotically stimulated SON.

Indexed as

Endoplasmic Reticulum StressOsmotic PressureActivating Transcription Factor 4AnimalsCyclic AMP Response Element-Binding ProteinDNA-Binding ProteinsEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHypothalamusMaleOrgan SpecificityRatsRats, Sprague-DawleyRegulatory Factor X Transcription FactorsRNA, MessengerTranscription Factor CHOPActivating Transcription Factor 4Atf4 protein, ratCREB3L1 protein, ratCyclic AMP Response Element-Binding ProteinDNA-Binding ProteinsEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsRegulatory Factor X Transcription FactorsRNA, MessengerTranscription Factor CHOPTranscription FactorsX-Box Binding Protein 1Xbp1 protein, rat

Identifiers

PMID25915053
PMCPMC4411032
OpenAlexW2085289756

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.