Evidence map›Paper›PMID 35883670›Full record

ArticleCells2022

VMP1 Regulated by chi-miR-124a Effects Goat Myoblast Proliferation, Autophagy, and Apoptosis through the PI3K/ULK1/mTOR Signaling Pathway.

Yufang Liu, Zuyang Zhou, Kunyu Li, Peng Wang, Yulin Chen, Shoulong Deng, Wenting Li, Kun Yu, Kejun Wang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 12 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

9 authors at 4 institutions in 1 country.

Yufang LiuCollege of Animal Sciences and Technology, Henan Agricultural University, Zhengzhou 450046, China.
Zuyang ZhouCollege of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056021, China.
Kunyu LiCollege of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056021, China.
Peng WangCollege of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056021, China.
Yulin ChenCollege of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056021, China.
Shoulong DengInstitute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100193, China.ORCID 0000-0003-1187-3037
Wenting LiCollege of Animal Sciences and Technology, Henan Agricultural University, Zhengzhou 450046, China.
Kun YuCollege of Animal Science and Technology, China Agricultural University, Beijing 100193, China.
Kejun WangCollege of Animal Sciences and Technology, Henan Agricultural University, Zhengzhou 450046, China.ORCID 0000-0003-4337-980X
Hebei University of Engineering · CNHenan Agricultural University · CNChina Agricultural University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of goat meat is determined by the growth speed of muscle fibers, and the autophagy and apoptosis of myoblast cells is a crucial process in the growth of muscle fibers. The rapid growth of muscle fibers occurs from one month old to nine months old in goats; however, the mechanisms of myoblast cells' autophagy and apoptosis in this process are still unknown. To identify candidate genes and signaling pathway mechanisms involved in myoblast apoptosis and autophagy, we compared the expression characteristics of longissimus dorsi tissues from Wu'an goats-a native goat breed of China-at 1 month old (mon1 group) and 9 months old (mon9 group). Herein, a total of 182 differentially expressed mRNAs (DEGs) in the mon1 vs. mon9 comparison, along with the KEGG enrichments, showed that the PI3K-Akt pathway associated with autophagy and apoptosis was significantly enriched. Among these DEGs, expression of vacuole membrane protein 1 (VMP1)-a key gene for the PI3K-Akt pathway-was significantly upregulated in the older goats relative to the 1-month-old goats. We demonstrated that VMP1 promotes the proliferation and autophagy of myoblasts, and inhibits their apoptosis. The integration analysis of miRNA-mRNA showed that miR-124a was a regulator of VMP1 in muscle tissue, and overexpression and inhibition of miR-124a suppressed the proliferation and autophagy of myoblasts. The PI3K/Akt/mTOR pathway was an important pathway for cell autophagy. Additionally, the activator of the PI3K/Akt/mTOR pathway, the expression of VMP1, and ULK1 were higher than the negative control, and the expression of mTOR was depressed. The expression of VMP1, ULK1, and mTOR was the opposite when the inhibitor was added to the myoblasts. These results show that the PI3K/Akt/mTOR pathway promoted the expression of VMP1 and ULK1. By using adenovirus-mediated apoptosis and proliferation assays, we found that that miR-124a inhibits myoblast proliferation and autophagy, and promotes their apoptosis by targeting VMP1. In conclusion, our results indicated that VMP1 was highly expressed in the LD muscle tissues of nine-month-old goats, and that it was regulated by miR-124a to inhibit myoblast cells' apoptosis through the PI3K/Akt/mTOR pathway, and to promote proliferation and autophagy. These findings contribute to the understanding of the molecular mechanisms involved in myoblast proliferation, autophagy, and apoptosis.

Indexed as

MicroRNAsPhosphatidylinositol 3-KinasesAnimalsApoptosisAutophagyCell ProliferationGoatsMyoblastsProto-Oncogene Proteins c-aktRNA, MessengerSignal TransductionTOR Serine-Threonine KinasesMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, MessengerTOR Serine-Threonine Kinasesapoptosisautophagygoatlongissimus dorsi tissuemiR-124aVMP1

Identifiers

PMID35883670
PMCPMC9319091
OpenAlexW4285802062

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.