2006
DOI: 10.1016/j.bcp.2006.01.012
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Investigation of the cytotoxicity of eukaryotic and prokaryotic antimicrobial peptides in intestinal epithelial cells in vitro

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Cited by 221 publications
(172 citation statements)
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“…National Clinical Laboratory standards), it is paramount that such an equally rapid cytotoxicity screen can be employed to detect selective toxicity for bacterial over human cells Cytotoxicity of melittin is well established in a range of mammalian cells, notably erythrocytes [12]. Its toxicity has also been detected in hepatocytes [16], enterocytes [13], intestinal goblet cells [13], and astrocytomas [29]. Incubation of Caco-2 cells for 24…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…National Clinical Laboratory standards), it is paramount that such an equally rapid cytotoxicity screen can be employed to detect selective toxicity for bacterial over human cells Cytotoxicity of melittin is well established in a range of mammalian cells, notably erythrocytes [12]. Its toxicity has also been detected in hepatocytes [16], enterocytes [13], intestinal goblet cells [13], and astrocytomas [29]. Incubation of Caco-2 cells for 24…”
Section: Discussionmentioning
confidence: 99%
“…For example, structure activity studies on the AMP, melittin, have generated large numbers of structural analogues [11]. Melittin is an amphipathic cationic linear 26-mer α-peptide that has cell penetrating activity as well as well-known cytotoxicity in erythrocytes [12] and enterocytes [13] and other mammalian cells [14]. Alongside phospholipase A2, it is a major constituent of the venom of Apis Mellifera, and has been found to cause apoptosis and necrosis in different cells [15,16], as well as agonist and antagonist actions on many cellular proteins including phospholipase A2 and ATPases (reviewed in [14]).…”
Section: Introductionmentioning
confidence: 99%
“…The number of dead cells was determined by an MTT cell proliferation assay after 24 h of incubation with the complexes. [15] This method is a colorimetric assay system which measures the reduction of a tetrazolium component (MTT) to an insoluble formazan product by the mitochondria of viable cells. The amount of color produced is directly proportional to the number of viable cells.…”
Section: Cytotoxic Effectmentioning
confidence: 99%
“…The number of living cells was determined using methyl thiazolyldiphenyl-tetrazolium bromide (MTT) assay (Sigma, Germany) based on the reduction of the tetrazolium salt, methyl thiazolyldiphenyl-tetrazolium bromide into a crystalline blue formazan product by the cellular oxidoreductases of viable cells (Maher and McClean, 2006). The resultant formazan crystal formation is proportional to the number of living cells.…”
Section: Cell Viabilitymentioning
confidence: 99%