Evidence map›Paper›PMID 38977335›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2024

[Cell membrane-penetrating capacity of hPP10-Cu, Zn-SOD fusion protein and its antioxidant and anti-inflammatory activity].

J Zhang, J Yao, Y Yang, F Wang, Q Zheng, X Li, C Liu

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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

J ZhangYuncheng Vocational Nursing College, Yuncheng 04400, China.
J YaoAnesthesia Surgery Center, Shenzhen Hospital of Southern Medical University, Shenzhen 518100, China.
Y YangDepartment of Urology, Shenzhen Hospital of Southern Medical University, Shenzhen 518100, China.
F WangDepartment of Urology, Hainan Provincial People's Hospital, Haikou 570100, China.
Q ZhengDepartment of Urology, Shenzhen Hospital of Southern Medical University, Shenzhen 518100, China.
X LiClinical Innovation and Research Center, Shenzhen Hospital of Southern Medical University, Shenzhen 518100, China.
C LiuChina Three Gorges University, Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, Yichang 443002, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the cell membrane-penetrating capacity of human cell-penetrating peptide hPP10 carrying human antioxidant protein Cu-Zn superoxide dismutase (Cu, Zn-SOD) and assess the antioxidant and anti-inflammatory activity of these fusion proteins.

methodsThe fusion protein hPP10-Cu, Zn-SOD was obtained by genetic engineering and identified by Western blotting. The membrane-penetrating ability of the fusion protein was evaluated by immunofluorescence assay, fluorescence colocalization assay and Western blotting, its SOD enzyme activity was detected using a commercial kit, and its effect on cell viability was assessed with MTT assay. In a HEK293 cell model of H2O2-induced oxidative stress, the effect of hPP10-Cu, Zn-SOD on cell apoptosis was analyzed with flow cytometry and RT-qPCR, and its antioxidant effect was assessed using reactive oxygen species (ROS) assay; its anti-inflammatory effect was evaluated in mouse model of TPA-induced ear inflammation by detecting expression of the inflammatory factors using RT-qPCR, Western blotting and immunohistochemistry.

resultsThe fusion protein hPP10-Cu, Zn-SOD was successfully obtained. Immunofluorescence assay confirmed obvious membrane penetration of this fusion protein in HEK293 cells, localized both in the cell membrane and the cell nuclei after cell entry. hPP10-Cu, Zn-SOD at the concentration of 5 μmol/L exhibited strong antioxidant activity with minimal impact on cell viability at the concentration up to 10 μmol/L. The fusion protein obviously inhibited apoptosis and decreased intracellular ROS level in the oxidative stress cell model and significantly reduced mRNA and protein expression of the inflammatory factors in the mouse model of ear inflammation.

conclusionThe fusion protein hPP10-Cu, Zn-SOD capable of penetrating the cell membrane possesses strong antioxidant and anti-inflammatory activities with only minimal cytotoxicity, demonstrating the value of hPP10 as an efficient drug delivery vector and the potential of hPP10-Cu, Zn-SOD in the development of skincare products.

Indexed as

Anti-Inflammatory AgentsAntioxidantsApoptosisCell-Penetrating PeptidesOxidative StressSuperoxide DismutaseAnimalsCell MembraneCell SurvivalHEK293 CellsHumansHydrogen PeroxideInflammationMiceReactive Oxygen SpeciesRecombinant Fusion ProteinsAnti-Inflammatory AgentsAntioxidantsCell-Penetrating PeptidesHydrogen PeroxideReactive Oxygen SpeciesRecombinant Fusion ProteinsSuperoxide Dismutaseanti-inflammatoryantioxidantCu-Zn superoxide dismutase Cu, Zn-SODenzyme activity assayhuman cell membrane penetrating peptide hPP10

Identifiers

PMID38977335
PMCPMC11237297

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