Xueqi Ma
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Xueqi Ma has a total of 30 co-authors. Here are the top co-authors by number of shared publications:
Juan Höfer
Escuela de Ciencias del Mar Pontificia Universidad Cato ´lica de Valparaı ´so Valparaı ´so Regio ´n de Valparaı ´so Chile
2 shared publications- Liang Xiao
Faculty of Naval Medicine, Naval Medical University, Shanghai, 200433, China
2 shared publications Xuecun Liu
Department of Occupational and Environmental Health Faculty of Naval Medicine Naval Medical University (Second Military Medical University) Shanghai China
2 shared publicationsFangbing Li
National Key Laboratory of Medical Immunology &Institute of Immunology, Navy Medical University, Shanghai, China
1 shared publicationHaiyan Zhang
Department of Healthcare Changhai Hospital Naval Medical University (Second Military Medical University) Shanghai China
1 shared publication- Jinggang Mo
Department of General Surgery Taizhou Central Hospital (Taizhou University Hospital) Taizhou University 318001 Taizhou Zhejiang Province P. R. China
1 shared publication
Latest Publications
- Open Access
- 15 April 2025
- Published by Frontiers Media SA in Frontiers in Marine Science
- Vol. 12, 1563258
Targeting metzincins to mitigate jellyfish blooms: a novel approach for conservation
Introduction: The modification of the marine ecological environment has led to the frequent occurrence of jellyfish blooms, causing global hazards. The budding reproduction of jellyfish polyps is a critical factor in their population size, yet there is limited understanding of the molecular mechanisms involved in this process. This study aims to explore the intrinsic regulatory factors of the budding of jellyfish Aurelia coerulea (A. coerulea) polyps from the perspective of jellyfish biotoxin and to develop new strategies for the management of jellyfish abundance.Methods: The main biological toxins of the A. coerulea polyp were screened through the integrated analysis of transcriptomic and proteomic data. The broad-spectrum metalloproteinase inhibitor, ethylenediaminetetraacetic acid (EDTA), was employed to treat polyps for observing its effect on the budding of A. coerulea polyps. Through conducting the detection of metzincin proteolytic activity, molecular docking and kinetic analysis, as well as transcriptomic analysis and RT-qPCR verification before and after EDTA treatment of the polyp, the key biological toxins and the mechanisms influencing polyp budding were clarified.Results: Four types of the metzincin family of metalloproteinases constituted the main biotoxins in the A. coerulea polyp. Among them, astacins (NAS) were the predominant metzincins of the A. coerulea polyp. We discovered that EDTA significantly inhibited the activity of metzincins and the budding of A. coerulea polyps. EDTA was capable of stably binding to the zinc-binding active sites of the four major types of metzincins in the A. coerulea polyp and could down-regulate the expression levels of key metzincin molecules and enrich multiple pathways related to development.Conclusion: This study elucidates the effects of metzincins on the budding of jellyfish polyps, providing a potential target for mitigating jellyfish blooms.
- 15 April 2025
- Published by Frontiers Media SA in Frontiers in Marine Science
- Vol. 12, 1563258
Open AccessTargeting metzincins to mitigate jellyfish blooms: a novel approach for conservation
Introduction: The modification of the marine ecological environment has led to the frequent occurrence of jellyfish blooms, causing global hazards. The budding reproduction of jellyfish polyps is a critical factor in their population size, yet there is limited understanding of the molecular mechanisms involved in this process. This study aims to explore the intrinsic regulatory factors of the budding of jellyfish Aurelia coerulea (A. coerulea) polyps from the perspective of jellyfish biotoxin and to develop new strategies for the management of jellyfish abundance.Methods: The main biological toxins of the A. coerulea polyp were screened through the integrated analysis of transcriptomic and proteomic data. The broad-spectrum metalloproteinase inhibitor, ethylenediaminetetraacetic acid (EDTA), was employed to treat polyps for observing its effect on the budding of A. coerulea polyps. Through conducting the detection of metzincin proteolytic activity, molecular docking and kinetic analysis, as well as transcriptomic analysis and RT-qPCR verification before and after EDTA treatment of the polyp, the key biological toxins and the mechanisms influencing polyp budding were clarified.Results: Four types of the metzincin family of metalloproteinases constituted the main biotoxins in the A. coerulea polyp. Among them, astacins (NAS) were the predominant metzincins of the A. coerulea polyp. We discovered that EDTA significantly inhibited the activity of metzincins and the budding of A. coerulea polyps. EDTA was capable of stably binding to the zinc-binding active sites of the four major types of metzincins in the A. coerulea polyp and could down-regulate the expression levels of key metzincin molecules and enrich multiple pathways related to development.Conclusion: This study elucidates the effects of metzincins on the budding of jellyfish polyps, providing a potential target for mitigating jellyfish blooms.
- Open Access
- 26 September 2024
- Published by Elsevier in Ecotoxicology and Environmental Safety
- Vol. 285, 117112
Copper-induced oxidative stress inhibits asexual reproduction of Aurelia coerulea polyps
- 26 September 2024
- Published by Elsevier in Ecotoxicology and Environmental Safety
- Vol. 285, 117112
Open AccessCopper-induced oxidative stress inhibits asexual reproduction of Aurelia coerulea polyps