期刊
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
卷 184, 期 -, 页码 776-786出版社
ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.06.145
关键词
Cobra venom cytotoxin; Secretome; Necroptosis
资金
- Fundamental Research Grant Scheme [FRGS/1/2018/SKK08/MUSM/03/1]
- Ministry of Higher Education, Malaysia
The study found that Naja sumatrana venom cytotoxin (sumaCTX) induced membrane permeabilization in MCF-7 cells at high concentrations, altering the secretome composition. High concentrations of sumaCTX caused the release of intracellular proteins, triggering necroptotic response in the cells.
Naja sumatrana venom cytotoxin (sumaCTX) is a basic protein which belongs to three-finger toxin family. It has been shown to induce caspase-dependent, mitochondrial-mediated apoptosis in MCF-7 cells at lower concentrations. This study aimed to investigate the alteration of secretome in MCF-7 cells following membrane permeabilization by high concentrations of sumaCTX, using label-free quantitative (LFQ) approach. The degree of membrane permeabilization of sumaCTX was determined by lactate dehydrogenase (LDH) assay and calceinpropidium iodide (PI) assays. LDH and calcein-PI assays revealed time-dependent membrane permeabilization within a narrow concentration range. However, as toxin concentrations increased, prolonged exposure of MCF-7 cells to sumaCTX did not promote the progression of membrane permeabilization. The secretome analyses showed that membrane permeabilization was an event preceding the release of intracellular proteins. Bioinformatics analyses of the LFQ secretome revealed the presence of 105 significantly distinguished proteins involved in metabolism, structural supports, inflammatory responses, and necroptosis in MCF-7 cells treated with 29.8 mu g/mL of sumaCTX. Necroptosis was presumably an initial stress response in MCF-7 cells when exposed to high sumaCTX concentration. Collectively, sumaCTX-induced the loss of membrane integrity in a concentrationdependent manner, whereby the cell death pattern of MCF-7 cells transformed from apoptosis to necroptosis with increasing toxin concentrations.
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