Proteomic analysis of oxidative stress response in human umbilical vein endothelial cells (HUVECs) : role of heme oxygenase 1 (HMOX1) in hypoxanthine-induced oxidative stress in HUVECs
2020 Translational Andrology and Urology. All rights reserved..
BACKGROUND: Erectile dysfunction (ED) is a well-known complication of diabetes, affecting up to 75% of diabetic men. Although the etiology of diabetic ED is multifactorial, endothelial dysfunction is considered to be a pillar of its pathophysiology. Endothelial dysfunction is caused by the harmful effects of high glucose levels and increased oxidative stress on the endothelial cells that comprise the vascular endothelium. The aim of this study was to identify the proteomic changes caused by high glucose-induced oxidative stress and explore the role of heme oxygenase 1 (HMOX1) in it.
METHODS: The cellular proteomic response to hypoxanthine-induced oxidative stress in human umbilical vein endothelial cells (HUVECs) was analyzed by isobaric tags for relative and absolute quantitation (iTRAQ) combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Differentially expressed proteins (DEPs) were analyzed through Network and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. Further validation assays was performed to validate the role of HMOX1.
RESULTS: The results showed that 66 and 76 DEPs were markedly upregulated and downregulated, respectively, for HUVECs oxidative stress. Among these proteins, we verified eight dysregulated genes by quantitative reverse transcription PCR, including nucleolin (NCL), X-ray repair cross-complementing protein 6 (XRCC6), ubiquinol-cytochrome C reductase binding protein (UQCRB), non-POU domain containing octamer binding (NONO), heme oxygenase 1 (HMOX1), nucleobindin 1 (NUCB1), DEK, and chromatin target of prmt1 (CHTOP). Further, using overexpression and genetic knockdown approaches, we found that HMOX1 was critical for the oxidative stress response in HUVECs.
CONCLUSIONS: We found that HMOX1 was closely related to the oxidative stress response induced by hypoxanthine. To the best of our knowledge, this study is the first overview of the responses of HUVECs to oxidative stress. The findings will contribute to analyses of the detailed molecular mechanisms involved in the pathogenesis of endothelial dysfunction and related molecular mechanisms in ED patients.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2020 |
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| Erschienen: |
2020 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:9 |
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| Enthalten in: |
Translational andrology and urology - 9(2020), 2 vom: 12. Apr., Seite 218-231 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Zhu, Pei [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Revised 14.04.2022 published: Print Citation Status PubMed-not-MEDLINE |
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| doi: |
10.21037/tau.2020.03.11 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM310027624 |
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| 100 | 1 | |a Zhu, Pei |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Proteomic analysis of oxidative stress response in human umbilical vein endothelial cells (HUVECs) |b role of heme oxygenase 1 (HMOX1) in hypoxanthine-induced oxidative stress in HUVECs |
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| 500 | |a published: Print | ||
| 500 | |a Citation Status PubMed-not-MEDLINE | ||
| 520 | |a 2020 Translational Andrology and Urology. All rights reserved. | ||
| 520 | |a BACKGROUND: Erectile dysfunction (ED) is a well-known complication of diabetes, affecting up to 75% of diabetic men. Although the etiology of diabetic ED is multifactorial, endothelial dysfunction is considered to be a pillar of its pathophysiology. Endothelial dysfunction is caused by the harmful effects of high glucose levels and increased oxidative stress on the endothelial cells that comprise the vascular endothelium. The aim of this study was to identify the proteomic changes caused by high glucose-induced oxidative stress and explore the role of heme oxygenase 1 (HMOX1) in it | ||
| 520 | |a METHODS: The cellular proteomic response to hypoxanthine-induced oxidative stress in human umbilical vein endothelial cells (HUVECs) was analyzed by isobaric tags for relative and absolute quantitation (iTRAQ) combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Differentially expressed proteins (DEPs) were analyzed through Network and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. Further validation assays was performed to validate the role of HMOX1 | ||
| 520 | |a RESULTS: The results showed that 66 and 76 DEPs were markedly upregulated and downregulated, respectively, for HUVECs oxidative stress. Among these proteins, we verified eight dysregulated genes by quantitative reverse transcription PCR, including nucleolin (NCL), X-ray repair cross-complementing protein 6 (XRCC6), ubiquinol-cytochrome C reductase binding protein (UQCRB), non-POU domain containing octamer binding (NONO), heme oxygenase 1 (HMOX1), nucleobindin 1 (NUCB1), DEK, and chromatin target of prmt1 (CHTOP). Further, using overexpression and genetic knockdown approaches, we found that HMOX1 was critical for the oxidative stress response in HUVECs | ||
| 520 | |a CONCLUSIONS: We found that HMOX1 was closely related to the oxidative stress response induced by hypoxanthine. To the best of our knowledge, this study is the first overview of the responses of HUVECs to oxidative stress. The findings will contribute to analyses of the detailed molecular mechanisms involved in the pathogenesis of endothelial dysfunction and related molecular mechanisms in ED patients | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Erectile dysfunction (ED) | |
| 650 | 4 | |a heme oxygenase 1 (HMOX1) | |
| 650 | 4 | |a human umbilical vein endothelial cells (HUVECs) | |
| 650 | 4 | |a hypoxanthine | |
| 650 | 4 | |a isobaric tags for relative and absolute quantitation (iTRAQ) | |
| 650 | 4 | |a liquid chromatography-tandem mass spectrometry (LC-MS/MS) | |
| 650 | 4 | |a oxidative stress | |
| 700 | 1 | |a Qi, Tao |e verfasserin |4 aut | |
| 700 | 1 | |a Huang, Zhan-Sen |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Hao |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Bo |e verfasserin |4 aut | |
| 700 | 1 | |a Feng, Jia-Xin |e verfasserin |4 aut | |
| 700 | 1 | |a Ma, Shuai |e verfasserin |4 aut | |
| 700 | 1 | |a Xiao, Heng-Jun |e verfasserin |4 aut | |
| 700 | 1 | |a Tang, Yu-Xin |e verfasserin |4 aut | |
| 700 | 1 | |a Liu, Wei |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Jun |e verfasserin |4 aut | |
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