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Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation

Purpose: To examine the differences in gene expression between ruptured and non-ruptured nucleus pulposus tissues of the intervertebral discs using gene chip technology. Methods: A total of 8 patients with nucleus pulposus from a lumbar disc herniation (LDH) undergoing discectomy in our hospital wer...

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Autores principales: Li, Xiaochun, Shen, Xueqiang, Wang, Zhiqiang, Jiang, Hong, Ma, Zhijia, Yu, Pengfei, Yu, Zhenhan, Qian, Xiang, Liu, Jintao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732013/
https://www.ncbi.nlm.nih.gov/pubmed/36506585
http://dx.doi.org/10.3389/fphar.2022.892594
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author Li, Xiaochun
Shen, Xueqiang
Wang, Zhiqiang
Jiang, Hong
Ma, Zhijia
Yu, Pengfei
Yu, Zhenhan
Qian, Xiang
Liu, Jintao
author_facet Li, Xiaochun
Shen, Xueqiang
Wang, Zhiqiang
Jiang, Hong
Ma, Zhijia
Yu, Pengfei
Yu, Zhenhan
Qian, Xiang
Liu, Jintao
author_sort Li, Xiaochun
collection PubMed
description Purpose: To examine the differences in gene expression between ruptured and non-ruptured nucleus pulposus tissues of the intervertebral discs using gene chip technology. Methods: A total of 8 patients with nucleus pulposus from a lumbar disc herniation (LDH) undergoing discectomy in our hospital were selected, including 4 ruptured and 4 non-ruptured herniated nucleus pulposus cases. Total RNA was extracted from cells by using TRIzol reagent. Nucleus pulposus cDNA probes of the two groups were obtained by the single marker method and hybridized with a human gene expression profiling chip (Agilent). The fluorescence signal images were scanned by a laser, and the obtained genes were analyzed by bioinformatics. Results: There were 75 differentially expressed genes with more than 2-fold-changes, of which 56 were up-regulated and 19 were down-regulated. The differential expression of THSD7A, which was up-regulated 18 times, was the most significant, followed by CCL5, AQP3 and SDC4. Conclusion: THSD7A can be used as a characteristic differentially expressed gene in human ruptured nucleus pulposus. Moreover, CCL5, AQP3 and SDC4 may improve the chemotaxis of stem cell migration for self-healing of damaged disc tissue, increase water uptake by nucleus accumbens cells, and inhibit the inflammatory response, thus delaying the process of intervertebral disc degeneration.
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spelling pubmed-97320132022-12-10 Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation Li, Xiaochun Shen, Xueqiang Wang, Zhiqiang Jiang, Hong Ma, Zhijia Yu, Pengfei Yu, Zhenhan Qian, Xiang Liu, Jintao Front Pharmacol Pharmacology Purpose: To examine the differences in gene expression between ruptured and non-ruptured nucleus pulposus tissues of the intervertebral discs using gene chip technology. Methods: A total of 8 patients with nucleus pulposus from a lumbar disc herniation (LDH) undergoing discectomy in our hospital were selected, including 4 ruptured and 4 non-ruptured herniated nucleus pulposus cases. Total RNA was extracted from cells by using TRIzol reagent. Nucleus pulposus cDNA probes of the two groups were obtained by the single marker method and hybridized with a human gene expression profiling chip (Agilent). The fluorescence signal images were scanned by a laser, and the obtained genes were analyzed by bioinformatics. Results: There were 75 differentially expressed genes with more than 2-fold-changes, of which 56 were up-regulated and 19 were down-regulated. The differential expression of THSD7A, which was up-regulated 18 times, was the most significant, followed by CCL5, AQP3 and SDC4. Conclusion: THSD7A can be used as a characteristic differentially expressed gene in human ruptured nucleus pulposus. Moreover, CCL5, AQP3 and SDC4 may improve the chemotaxis of stem cell migration for self-healing of damaged disc tissue, increase water uptake by nucleus accumbens cells, and inhibit the inflammatory response, thus delaying the process of intervertebral disc degeneration. Frontiers Media S.A. 2022-11-25 /pmc/articles/PMC9732013/ /pubmed/36506585 http://dx.doi.org/10.3389/fphar.2022.892594 Text en Copyright © 2022 Li, Shen, Wang, Jiang, Ma, Yu, Yu, Qian and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Li, Xiaochun
Shen, Xueqiang
Wang, Zhiqiang
Jiang, Hong
Ma, Zhijia
Yu, Pengfei
Yu, Zhenhan
Qian, Xiang
Liu, Jintao
Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title_full Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title_fullStr Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title_full_unstemmed Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title_short Gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
title_sort gene expression profiling in nucleus pulposus of human ruptured lumbar disc herniation
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732013/
https://www.ncbi.nlm.nih.gov/pubmed/36506585
http://dx.doi.org/10.3389/fphar.2022.892594
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