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pmid:35990856

Identification of miRNA-mRNA Pairs in Relation to TNF-α/IL-1β Induced Inflammatory Response in Intervertebral Disc Degeneration.

Ye Wei · Yulin Chen · Han Su · Chunyan Ling · Guangtian Huang · Dongling Wang · Guanghui Chen

Evidence-based complementary and alternative medicine : eCAM · 2022 doi:10.1155/2022/3374091

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Identification of miRNA-mRNA Pairs in Relation to TNF-α/IL-1β Induced Inflammatory Response in Intervertebral Disc Degeneration.
doi
10.1155/2022/3374091
pmid
35990856
authors array · 7 items
[0]
Ye Wei
[1]
Yulin Chen
[2]
Han Su
[3]
Chunyan Ling
[4]
Guangtian Huang
[5]
Dongling Wang
[6]
Guanghui Chen
journal
Evidence-based complementary and alternative medicine : eCAM
year
2022
abstract
Objective: The determination of miRNA-mRNA pairs for intervertebral disc degeneration (IVDD) regulated by pro-inflammatory cytokines were investigated. Methods: Two dataset (accession number GSE27494 and GSE41883 from platform GPL1352) of expression profiling was downloaded from Gene Expression Omnibus (GEO). The annulus cells were isolated from annulus fibrosus in patients with degenerative disc disease. The cells were then cultured in a three-dimensional (3D) collagen containing with/without proinflammatory cytokines (tumor necrosis factor alpha (TNF-α) or interleukin beta (IL-1β)). After being cultured for 14 days, the isolated total RNA was analyzed via microarray, and the expression array data were obtained using BRB-Array Tools followed by analyzing the differentially expressed genes (DEGs) and the prediction of potential miRNA targets of hub genes through online database. Results: Firstly, 52 and 296 DEGs were found in IL-1β- and TNF-α-induced annulus cells, respectively, of these there had 42 common DEGs (co-DEGs) with 34 increased transcripts and 8 reduced ones. Based on the GO and KEGG software, these co-DEGs were mainly enriched in the response to lipopolysaccharide (LPS) and molecule of bacterial origin, the regulation of receptor ligand activity and signaling receptor activator activity, as well as the following signaling pathways, including TNF signaling pathway, IL-17 signaling pathway, and NF-κB signaling pathway. Top hub genes (CXCL1, CXCL2, CXCL8, IL1Β and PTGS2) regulated by several potential microRNAs were involved in TNF-α/IL-1β treated annulus cells. Conclusions: Several candidate genes regulated by miRNAs caused by TNF-α/IL-1β in the annulus cells were found, which will guide diagnosis and treatment for degenerative disc disease.
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Using the unpaired t-test with statistical significance as the threshold of adjusted P value < 0.05 and log fold change (Log2FC) ≥ 1.5, the DEGs were screened, followed by generating a volcano plot of DEGs with statistical significance using BRB Array Tools (version 3.7) strictly according to the user's manual.
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Using the unpaired t-test with statistical significance as the threshold of adjusted P value < 0.05 and log fold change (Log2FC) ≥ 1.5, the DEGs were screened, followed by generating a volcano plot of DEGs with statistical significance using BRB Array Tools (version 3.7) strictly according to the user's manual.
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IL-1β treatment produced 52 DEGs, TNF-α treatment produced 296 DEGs, and the treatments shared 42 co-DEGs, including 34 upregulated and 8 downregulated genes.
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Firstly, 52 and 296 DEGs were found in IL-1β- and TNF-α-induced annulus cells, respectively, of these there had 42 common DEGs (co-DEGs) with 34 increased transcripts and 8 reduced ones.
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IL-1 Exposure Significantly increases gene expression of BDNF, NTF3 and NRP2 as well as NGF Production in Human Annulus Cells
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Using the unpaired t-test with statistical significance as the threshold of adjusted P value < 0.05 and log fold change (Log2FC) ≥ 1.5, the DEGs were screened, followed by generating a volcano plot of DEGs with statistical significance using BRB Array Tools (version 3.7) strictly according to the user's manual.
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Complete file
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The annulus cells were isolated from annulus fibrosus in patients with degenerative disc disease. The cells were then cultured in a three-dimensional (3D) collagen containing with/without proinflammatory cytokines (tumor necrosis factor alpha (TNF-α) or interleukin beta (IL-1β)). After being cultured for 14 days, the isolated total RNA was analyzed via microarray, and the expression array data were obtained using BRB-Array Tools followed by analyzing the differentially expressed genes (DEGs) and the prediction of potential miRNA targets of hub genes through online database.\nResults: Firstly, 52 and 296 DEGs were found in IL-1β- and TNF-α-induced annulus cells, respectively, of these there had 42 common DEGs (co-DEGs) with 34 increased transcripts and 8 reduced ones. 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