Literature DB >> 33925349

Proteomic Changes during the Dermal Toxicity Induced by Nemopilema nomurai Jellyfish Venom in HaCaT Human Keratinocyte.

Indu Choudhary1, Duhyeon Hwang1,2, Jinho Chae3, Wonduk Yoon3, Changkeun Kang1,2, Euikyung Kim1,2.   

Abstract

Jellyfish venom is well known for its local skin toxicities and various lethal accidents. The main symptoms of local jellyfish envenomation include skin lesions, burning, prickling, stinging pain, red, brown, or purplish tracks on the skin, itching, and swelling, leading to dermonecrosis and scar formation. However, the molecular mechanism behind the action of jellyfish venom on human skin cells is rarely understood. In the present study, we have treated the human HaCaT keratinocyte with Nemopilema nomurai jellyfish venom (NnV) to study detailed mechanisms of actions behind the skin symptoms after jellyfish envenomation. Using two-dimensional gel electrophoresis (2-DE) and matrix-assisted laser desorption-ionization time-of-flight mass spectrometry (MALDI-TOF/MS), cellular changes at proteome level were examined. The treatment of NnV resulted in the decrease of HaCaT cell viability in a concentration-dependent manner. Using NnV (at IC50), the proteome level alterations were determined at 12 h and 24 h after the venom treatment. Briefly, 70 protein spots with significant quantitative changes were picked from the gels for MALDI-TOF/MS. In total, 44 differentially abundant proteins were successfully identified, among which 19 proteins were increased, whereas 25 proteins were decreased in the abundance levels comparing with their respective control spots. DAPs involved in cell survival and development (e.g., Plasminogen, Vinculin, EMILIN-1, Basonuclin2, Focal adhesion kinase 1, FAM83B, Peroxisome proliferator-activated receptor-gamma co-activator 1-alpha) decreased their expression, whereas stress or immune response-related proteins (e.g., Toll-like receptor 4, Aminopeptidase N, MKL/Myocardin-like protein 1, hypoxia up-regulated protein 1, Heat shock protein 105 kDa, Ephrin type-A receptor 1, with some protease (or peptidase) enzymes) were up-regulated. In conclusion, the present findings may exhibit some possible key players during skin damage and suggest therapeutic strategies for preventing jellyfish envenomation.

Entities:  

Keywords:  2-DE; HaCaT cell; MALDI-TOF/MS; Nemopilema nomurai jellyfish; dermal toxicity

Year:  2021        PMID: 33925349     DOI: 10.3390/toxins13050311

Source DB:  PubMed          Journal:  Toxins (Basel)        ISSN: 2072-6651            Impact factor:   4.546


  67 in total

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4.  Rapamycin Modulates Glucocorticoid Receptor Function, Blocks Atrophogene REDD1, and Protects Skin from Steroid Atrophy.

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6.  EMILIN-1 regulates the amount of oxytalan fiber formation in periodontal ligaments in vitro.

Authors:  Yuka Nakatomi; Eichi Tsuruga; Kazuki Nakashima; Yoshihiko Sawa; Hiroyuki Ishikawa
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8.  Cytokines and glucocorticoids differentially regulate APN/CD13 and DPPIV/CD26 enzyme activities in cultured human dermal fibroblasts.

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Authors:  H Tseng; H Green
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10.  Transcriptome and venom proteome of the box jellyfish Chironex fleckeri.

Authors:  Diane L Brinkman; Xinying Jia; Jeremy Potriquet; Dhirendra Kumar; Debasis Dash; David Kvaskoff; Jason Mulvenna
Journal:  BMC Genomics       Date:  2015-05-27       Impact factor: 3.969

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