Evidence map›Paper›PMID 31699966›Full record

ArticleCell death & disease2019

SPARCL1 promotes C2C12 cell differentiation via BMP7-mediated BMP/TGF-β cell signaling pathway.

YuXin Wang, ShuaiYu Liu, YunQin Yan, ShuFeng Li, HuiLi Tong

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. The oncogenic functions of SPARCL1 in bladder cancer.Journal of cellular and molecular medicine · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Sparcl1 and Atherosclerosis.Journal of inflammation research · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

YuXin WangThe Laboratory of Cell and Developmental Biology, Northeast Agricultural University, Harbin, Heilongjiang, 150030, China.
ShuaiYu LiuThe Laboratory of Cell and Developmental Biology, Northeast Agricultural University, Harbin, Heilongjiang, 150030, China.
YunQin YanThe Laboratory of Cell and Developmental Biology, Northeast Agricultural University, Harbin, Heilongjiang, 150030, China.
ShuFeng LiThe Laboratory of Cell and Developmental Biology, Northeast Agricultural University, Harbin, Heilongjiang, 150030, China.
HuiLi TongThe Laboratory of Cell and Developmental Biology, Northeast Agricultural University, Harbin, Heilongjiang, 150030, China. tonghuili2004@163.com.
Northeast Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extracellular matrix (ECM) is known to regulate tissue development and cell morphology, movement, and differentiation. SPARCL1 is an ECM protein, but its role in mouse cell differentiation has not been widely investigated. The results of western blotting and immunofluorescence showed that SPARCL1 is associated with the repair of muscle damage in mice and that SPARCL1 binds to bone morphogenetic protein 7 (BMP7) by regulating BMP/transforming growth factor (TGF)-β cell signaling. This pathway promotes the differentiation of C2C12 cells. Using CRISPR/Cas9 technology, we also showed that SPARCL1 activates BMP/TGF-β to promote the differentiation of C2C12 cells. BMP7 molecules were found to interact with SPARCL1 by immunoprecipitation analysis. Western blotting and immunofluorescence were performed to verify the effect of BMP7 on C2C12 cell differentiation. Furthermore, SPARCL1 was shown to influence the expression of BMP7 and activity of the BMP/TGF-β signaling pathway. Finally, SPARCL1 activation was accompanied by BMP7 inhibition in C2C12 cells, which confirmed that SPARCL1 affects BMP7 expression and can promote C2C12 cell differentiation through the BMP/TGF-β pathway. The ECM is essential for muscle regeneration and damage repair. This study intends to improve the understanding of the molecular mechanisms of muscle development and provide new treatment ideas for muscle injury diseases.

Indexed as

Cell DifferentiationGene Expression RegulationAnimalsBone Morphogenetic Protein 7Calcium-Binding ProteinsExtracellular Matrix ProteinsMaleMiceMice, Inbred ICRMuscle, SkeletalMyoblastsSignal TransductionTransforming Growth Factor betabmp7 protein, mouseBone Morphogenetic Protein 7Calcium-Binding ProteinsExtracellular Matrix ProteinsSparcl1 protein, mouseTransforming Growth Factor beta

Identifiers

PMID31699966
PMCPMC6838091
OpenAlexW2988746844

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.