Evidence map›Paper›PMID 36696024›Full record

ArticleMolecular biology reports2023

Comparative transcriptome analysis provides insight into the molecular targets and signaling pathways of deer TGF-1 regulating chondrocytes proliferation and differentiation.

Zhenwei Zhou, Jinghong Zhong, Jingcheng Zhang, Jie Yang, Xiangyang Leng, Baojin Yao, Xukai Wang, Haisi Dong

Abstract read
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In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 6 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 1 institution in 1 country.

Zhenwei Zhou *Northeast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Jinghong Zhong *Northeast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Jingcheng ZhangNortheast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Jie YangCollege of traditional Chinese medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Xiangyang LengNortheast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Baojin YaoNortheast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China.
Xukai WangAffiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China. wangxukai_2003@163.com.
Haisi DongNortheast Asia Institute of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, 130000, Jilin, China. adonghaisi@163.com.
Changchun University of Chinese Medicine · CN

Funding

Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine ZYYCXTD-D-202001Jilin Province Young and Middle-aged Science and Technology Innovation and Entrepreneurship Outstanding Talent (team) Project 20210509001RQNational Natural Science Foundation of China 81973887
6 · The paper itself

Abstract

backgroundChondrocytes are the only cell components in the cartilage, which has the poor regeneration ability. Thus, repairing damaged cartilage remains a huge challenge. Sika deer antlers are mainly composed of cartilaginous tissues that have an astonishing capacity for repair and renewal. Our previous study has demonstrated the transforming growth factor β (TGF-β1) is considered to be a key molecule involved in rapid growth, with the strongest expression in the cartilage layer. However, it remains to be clarified whether deer TGF-β1 has significantly different function from other species such as mouse, and what is the molecular mechanism of regulating cartilage growth.

methodsPrimary chondrocytes was collected from new born mouse rib cartilage. The effect of TGF-β1 on primary chondrocytes viability was elucidated by RNA sequencing (RNA-seq) technology combined with validation methods such as quantitative real-time polymerase chain reaction (qRT-PCR) and immunofluorescence assay (IFA). Differential expression genes were identified using the DEGseq package.

resultsOur results demonstrated that the overexpression of deer TGF-β1 possibly promoted chondrocyte proliferation and extracellular matrix (ECM) synthesis, while simultaneously suppressing chondrocyte differentiation through regulating transcription factors, growth factors, ECM related genes, proliferation and differentiation marker genes, such as Comp, Fgfr3, Atf4, Stat1 etc., and signaling pathways such as the MAPK signaling pathway, inflammatory mediator regulation of TRP channels etc. In addition, by comparing the amino acid sequence and structures between the deer TGF-β1 and mouse TGF-β1, we found that deer TGF-β1 and mouse TGF-β1 proteins are mainly structurally different in arm domains, which is the main functional domain. Phenotypic identification results showed that deer TGF-β1 may has stronger function than mouse TGF-β1.

conclusion​These results suggested that deer TGF-β1 has the ability to promote chondrogenesis by regulating chondrocyte proliferation, differentiation and ECM synthesis. This study provides insights into the molecular mechanisms underlying the effects of deer TGF-β1 on chondrocyte viability.

Indexed as

ChondrocytesDeerAnimalsCell DifferentiationCell ProliferationCells, CulturedChondrogenesisGene Expression ProfilingMiceSignal TransductionTransforming Growth Factor beta1Transforming Growth Factor beta1ChondrogenesisDeer TGF-β1Mouse TGF-β1Primary chondrocytesRNA-Seq

Identifiers

PMID36696024
OpenAlexW4317941588

What Socratic holds

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Registered trials

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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 Socratic graph.