Evidence map›Paper›PMID 32423812›Full record

ArticleBiochemical and biophysical research communications2020

UGGT1 retains proinsulin in the endoplasmic reticulum in an arginine dependent manner.

Jaeyong Cho, Masaki Hiramoto, Yuka Masaike, Satoshi Sakamoto, Yoichi Imai, Yumi Imai, Hiroshi Handa, Takeshi Imai

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. UDP-Glucose: A Cereblon-Dependent Glucokinase Protein Degrader.International journal of molecular sciences · 2022
    Article
  4. Review
  5. Chorionic gonadotropin stimulates maternal hepatocyte proliferation during pregnancy.Biochemical and biophysical research communications · 2021
    Article
  6. 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 5 institutions in 2 countries.

Jaeyong ChoDepartment Aging Intervention, National Center for Geriatrics and Gerontology, Obu, Aichi, 474-8511, Japan. Electronic address: jaeyong420@gmail.com.
Masaki HiramotoDepartment Aging Intervention, National Center for Geriatrics and Gerontology, Obu, Aichi, 474-8511, Japan; Department of Biochemistry, Tokyo Medical University, Shinjyuku, Tokyo 160-8402, Japan. Electronic address: hiramoto@tokyo-med.ac.jp.
Yuka MasaikeDepartment of Nanoparticle Translational Research, Tokyo Medical University, Shinjyuku, Tokyo, 160-8402, Japan. Electronic address: yukamasaike@gmail.com.
Satoshi SakamotoSchool of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Kanagawa, 223-8503, Japan. Electronic address: ssakamoto@bio.titech.ac.jp.
Yoichi ImaiDepartment of Hematology/Oncology, Research Hospital, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan. Electronic address: imaiyo-tky@umin.ac.jp.
Yumi ImaiDepartment of Internal Medicine, Fraternal Order of Eagles Diabetes Research Center, University of Iowa Carver College of Medicine, Iowa City, IA, 52242, USA. Electronic address: yumi-imai@uiowa.edu.
Hiroshi HandaDepartment of Nanoparticle Translational Research, Tokyo Medical University, Shinjyuku, Tokyo, 160-8402, Japan. Electronic address: hhanda@tokyo-med.ac.jp.
Takeshi ImaiDepartment Aging Intervention, National Center for Geriatrics and Gerontology, Obu, Aichi, 474-8511, Japan. Electronic address: timai@ncgg.go.jp.
Tokyo Medical University · JPNational Center for Geriatrics and Gerontology · JPTokyo Institute of Technology · JPTokyo University of Science · JPUniversity of Iowa · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Amy Leanne Ryan · 1998 to 2026
$30.5M
Role of Lipid Droplet Proteins in Islet Function in Diabetes and ObesityR01DK090490 · NIDDK · UNIVERSITY OF IOWA · PI IMAI, YUMI · 2011 to 2025
$5.0M
NIDDK NIH HHS P30 DK054759NIDDK NIH HHS R01 DK090490
6 · The paper itself

Abstract

We sought to clarify a pathway by which L- and dD-arginine simulate insulin secretion in mice and cell lines and obtained the following novel two findings. (1) Using affinity magnetic nanobeads technology, we identified that proinsulin is retained in the endoplasmic reticulum (ER) through UDP-glucose:glycoprotein glucosyltransferase 1 (UGGT1) when arginine availability is limited. (2) L- and d-arginine release proinsulin from UGGT1 through competition with proinsulin and promote exit of proinsulin from the ER to Golgi apparatus. The ability of arginine to release proinsulin from UGGT1 closely correlates with arginine-induced insulin secretion in several models of β cells indicating that UGGT1-proinsulin interaction regulates arginine-induced insulin secretion.

Indexed as

AnimalsArginineCells, CulturedEndoplasmic ReticulumGlucosyltransferasesHEK293 CellsHumansInsulin-Secreting CellsInsulin SecretionMaleMiceMice, TransgenicModels, MolecularProinsulinArginineGlucosyltransferasesProinsulinUGGT1 protein, mouseArginineEndoplasmicInsulinReticulumUGGT1

Identifiers

PMID32423812
PMCPMC7863631
OpenAlexW3025432733

What OpenQuestion holds

Textmetadata
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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.