2020
DOI: 10.1016/j.bioelechem.2020.107550
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Correlation between the loss of intracellular molecules and cell viability after cell electroporation

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Cited by 29 publications
(15 citation statements)
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“…Therefore, the factors released from irreversibly electroporated cells presumably play several roles, including promotion of cell viability and enhancement of cell migration. Similar results were obtained by our recent study, where we showed that some irreversibly electroporated cells can be rescued by supplementing the medium with compounds obtained from irreversibly electroporated cells [ 24 ]. We determined that the intracellular molecules that contribute to the increase in cell viability are larger than 30 kDa.…”
Section: Discussionsupporting
confidence: 90%
See 1 more Smart Citation
“…Therefore, the factors released from irreversibly electroporated cells presumably play several roles, including promotion of cell viability and enhancement of cell migration. Similar results were obtained by our recent study, where we showed that some irreversibly electroporated cells can be rescued by supplementing the medium with compounds obtained from irreversibly electroporated cells [ 24 ]. We determined that the intracellular molecules that contribute to the increase in cell viability are larger than 30 kDa.…”
Section: Discussionsupporting
confidence: 90%
“…Interestingly, the rate and magnitude of the IRE-induced release of DAMPs, namely ATP and HMGB1, were reported to be much greater than those induced by other treatment modalities, such as ionizing radiation and chemotherapy [ 21 ]. Our previous study also demonstrated that cell death following cell electroporation is at least partially related to leakage of intracellular molecules [ 24 ].…”
Section: Introductionmentioning
confidence: 99%
“…The damage caused to the tissue by EP-related therapies can elicit ICD and promote a proinflammatory milieu and the recruitment of antigen presenting cells (APC) where tumor-specific antigens (TSA) and tumor associated antigens (TAA) might be captured and presented by APCs to T cells, leading to adaptive immune responses [ 112 , 113 , 114 , 115 , 116 , 117 ]. In fact, RE alone or in combination with bleomycin can lead to the leakage of cytoplasmatic molecules related to ICD and the activation of proinflammatory markers [ 114 , 118 , 119 , 120 ]. The main immunostimulatory molecules related to RE include: adenosine triphosphate (ATP) release, calreticulin (CRT) translocation to cell membrane, release of the non-histone, protein high mobility group box 1 (HMGB1), induction of heat shock protein family (HSP70) stress response and other proinflammatory genes [ 114 , 121 , 122 ].…”
Section: Immunological Aspects Of Reversible Electroporation and Electrochemotherapymentioning
confidence: 99%
“…When the cells loaded with the indicator are electroporated with the interest ions, fluorescence increase can be observed using a fluorescence microscope or flow cytometry. Monitoring the extracellular release of membrane-impermeable intracellular molecules can detect electroporation [ 28 , 29 , 30 ]. The efflux of cell-impermeable small molecules can be analyzed by appropriate methods.…”
Section: Introductionmentioning
confidence: 99%