Evidence map›Paper›PMID 38334628›Full record

ArticleCells2024

High Glucose Levels Promote Switch to Synthetic Vascular Smooth Muscle Cells via Lactate/GPR81.

Jing Yang, Glenn R Gourley, Adam Gilbertsen, Chi Chen, Lei Wang, Karen Smith, Marion Namenwirth, Libang Yang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Jing YangHubei Key Laboratory of Embryonic Stem Cell Research, Hubei University of Medicine, Shiyan 442000, China.
Glenn R GourleyDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Adam GilbertsenDepartment of Medicine, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Chi ChenDepartment of Food Science and Nutrition, CFANS, University of Minnesota, St Paul, MN 55108, USA.ORCID 0000-0001-9703-604X
Lei WangDepartment of Food Science and Nutrition, CFANS, University of Minnesota, St Paul, MN 55108, USA.
Karen SmithDepartment of Medicine, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Marion NamenwirthDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Libang YangDepartment of Medicine, University of Minnesota Medical School, Minneapolis, MN 55455, USA.ORCID 0000-0002-9318-6320
University of Minnesota · USUniversity of Minnesota Medical Center · USHubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperglycemia, lipotoxicity, and insulin resistance are known to increase the secretion of extracellular matrix from cardiac fibroblasts as well as the activation of paracrine signaling from cardiomyocytes, immune cells, and vascular cells, which release fibroblast-activating mediators. However, their influences on vascular smooth muscle cells (vSMCs) have not been well examined. This study aimed to investigate whether contractile vascular vSMCs could develop a more synthetic phenotype in response to hyperglycemia. The results showed that contractile and synthetic vSMCs consumed high glucose in different ways. Lactate/GPR81 promotes the synthetic phenotype in vSMCs in response to high glucose levels. The stimulation of high glucose was associated with a significant increase in fibroblast-like features: synthetic vSMC marker expression, collagen 1 production, proliferation, and migration. GPR81 expression is higher in blood vessels in diabetic patients and in the high-glucose, high-lipid diet mouse. The results demonstrate that vSMCs assume a more synthetic phenotype when cultured in the presence of high glucose and, consequently, that the high glucose could trigger a vSMC-dependent cardiovascular disease mechanism in diabetes via lactate/GPR81.

Indexed as

HyperglycemiaMuscle, Smooth, VascularAnimalsCell ProliferationCells, CulturedGlucoseHumansLactic AcidMiceReceptors, G-Protein-CoupledGlucoseHcar1 protein, mouseLactic AcidReceptors, G-Protein-CoupleddiabetesglucoseGPR81lactatephenotype changesmooth muscle cellsTallyHo mousevascular complication

Identifiers

PMID38334628
PMCPMC10854508
OpenAlexW4391254427

What OpenQuestion holds

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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.