Evidence map›Paper›PMID 29320716›Full record

ArticleMetabolism: clinical and experimental2018

Distinct roles of systemic and local actions of insulin on pancreatic β-cells.

Takumi Kitamoto, Kenichi Sakurai, Eun Young Lee, Koutaro Yokote, Domenico Accili, Takashi Miki

Open access · greenAbstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Misfolded proinsulin impairs processing of precursor of insulin receptor and insulin signaling in β cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  5. Diet-Induced Obese Mice and Leptin-DeficientInternational journal of molecular sciences · 2019
    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

6 authors at 2 institutions in 2 countries.

Takumi KitamotoDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan; Department of Clinical Cell Biology and Medicine, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan; Division of Endocrinology, Department of Medicine, Columbia University, New York 10032, USA.
Kenichi SakuraiCenter for Preventive Medical Sciences, Chiba University, Chiba 263-8522, Japan.
Eun Young LeeDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Koutaro YokoteDepartment of Clinical Cell Biology and Medicine, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Domenico AcciliDivision of Endocrinology, Department of Medicine, Columbia University, New York 10032, USA.
Takashi MikiDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan. Electronic address: tmiki@faculty.chiba-u.jp.
Chiba University · JPColumbia University · US

Funding

Translational Biomarker Analytical Core (TBAC)P30DK063608 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Anthony W Ferrante · 2003 to 2026
$36.7M
MECHANISMS OF BETA CELL FAILURER01DK064819 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ACCILI, DOMENICO · 2003 to 2025
$10.5M
NIDDK NIH HHS P30 DK063608NIDDK NIH HHS R01 DK064819
6 · The paper itself

Abstract

objectivePancreatic β-cell mass and function are critical in glucose homeostasis. Their regulatory mechanisms have been studied principally under experimental conditions of reduced β-cell numbers, such as β-cell ablation and partial pancreatectomy. In the present study, we generated an opposite mouse model with an excessive amount of ectopic β-cells, and analyzed its consequence on β-cell mass and survival.

methodsMice underwent sub-renal transplantation (SRT) of pseudo-islets generated from a pancreatic β-cell line MIN6 or intra-pancreatic transplantation (IPT) of MIN6 cells, and morphological and functional changes of their endocrine pancreata were analyzed. Cellular fate of pancreatic β-cells after transplantation was traced using RipCre:Rosa26-tdTomato mice. By using MIN6 cells, we evaluated the roles of extracellular glucose, membrane potential, and insulin signaling on β-cell survival.

resultsSRT mice developed severe, progressive hypoglycemia associated with marked reduction in insulin-positive (Ins

conclusionInsulin plays distinct roles in β-cell survival and β-cell mass regulation through its local and systemic actions on β-cells, respectively.

Indexed as

AnimalsCell LineCell SurvivalGlucoseHomeostasisHypoglycemiaInsulinInsulin-Secreting CellsMiceSignal TransductionGlucoseInsulinHypoglycemiaInsulin signalingβ-cell mass regulationβ-Cell survival

Identifiers

PMID29320716
PMCPMC7391221
OpenAlexW2782223966

What OpenQuestion holds

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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.