Evidence map›Paper›PMID 33098866›Full record

ArticleBiophysical journal2020

Cell-Type-Specific Expression Pattern of Proton-Sensing Receptors and Channels in Pituitary Gland.

Kai Wang, Karla Kretschmannova, Rafael M Prévide, Kosara Smiljanic, Qing Chen, Patrick A Fletcher, Arthur Sherman, Stanko S Stojilkovic

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. FOXO1 regulates expression of Neurod4 in the pituitary gland.Molecular and cellular endocrinology · 2024
    Article
  4. 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

8 authors at 2 institutions in 1 country.

Kai WangSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Karla KretschmannovaSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Rafael M PrévideSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Kosara SmiljanicSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Qing ChenSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Patrick A FletcherLaboratory of Biological Modeling, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
Arthur ShermanLaboratory of Biological Modeling, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
Stanko S StojilkovicSection on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland. Electronic address: stojilks@mail.nih.gov.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institutes of Health · US

Funding

INTRACELLULAR SIGNALING IN ENDOCRINE CELLSZ01HD000195 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STOJILKOVIC, STANKO S. · 1994 to 2008
$2.4M
Mathematical Modeling of Neurons and Endocrine CellsZIADK013028 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SHERMAN, ARTHUR · 2009 to 2025
$1.7M
Mathematical Modeling of Neurons and Endocrine CellsZ01DK013028 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SHERMAN, ARTHUR · 2007 to 2008
$208k
Intramural NIH HHS Z01 DK013028Intramural NIH HHS Z01 HD000195
6 · The paper itself

Abstract

In mammalian cells, extracellular protons act as orthosteric and allosteric ligands for multiple receptors and channels. The aim of this study is to identify proton sensors in the rat pituitary gland. qRT-PCR analysis indicated the expression of G-protein-coupled receptor 68 gene (Gpr68) and acid-sensing ion channel (ASIC) genes Asic1, Asic2, and Asic4 in anterior pituitary cells and Asic1 and Asic2 in immortalized GH3 pituitary cells. Asic1a and Asic2b were the dominant splice isoforms. Single anterior pituitary cell RNA sequencing and immunocytochemical analysis showed that nonexcitable folliculostellate cells express GPR68 gene and protein, whereas excitable secretory cells express ASIC genes and proteins. Asic1 was detected in all secretory cell types, Asic2 in gonadotrophs, thyrotrophs, and somatotrophs, and Asic4 in lactotrophs. Extracellular acidification activated two types of currents in a concentration-dependent manner: a fast-developing, desensitizing current with an estimated EC

Indexed as

Acid Sensing Ion ChannelsProtonsAnimalsNeuronsPituitary GlandProtein IsoformsRatsAcid Sensing Ion ChannelsProtein IsoformsProtons

Identifiers

PMID33098866
PMCPMC7732776
OpenAlexW3094186928

What OpenQuestion holds

Textmetadata
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.