Bovine lactoferricin causes apoptosis in Jurkat T-leukemia cells by sequential permeabilization of the cell membrane and targeting of mitochondria

• Published in: Experimental cell research 2007-07, Vol.313 (12), p.2634-2650
• Main Authors: Mader, Jamie S., Richardson, Angela, Salsman, Jayme, Top, Deniz, de Antueno, Roberto, Duncan, Roy, Hoskin, David W.
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; Animals; APOPTOSIS; Apoptosis - drug effects; Biotinylation; Bovine lactoferricin; CATTLE; Cell Line, Transformed; Cell Membrane - drug effects; Cell Membrane - metabolism; Cell Membrane Permeability - drug effects; CELL MEMBRANES; Cellular biology; Cytochrome c; Cytochromes c - secretion; CYTOPLASM; DEATH; DNA Fragmentation - drug effects; ELECTRON MICROSCOPY; Endocytosis - drug effects; FIBROBLASTS; Fibroblasts - cytology; Fibroblasts - drug effects; Humans; Jurkat Cells; Lactoferrin - pharmacology; LEUKEMIA; Liposome; Membrane Potential, Mitochondrial - drug effects; MITOCHONDRIA; Mitochondria - drug effects; Mitochondria - secretion; Mitochondria - ultrastructure; Mitochondrion; Molecular biology; PEPTIDES; Receptors, Cell Surface - metabolism; T-leukemia; T-Lymphocytes - cytology; T-Lymphocytes - drug effects; T-Lymphocytes - ultrastructure; TOXICITY
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/j.yexcr.2007.05.015

Bovine lactoferricin (LfcinB) is a cationic antimicrobial peptide that kills Jurkat T-leukemia cells by the mitochondrial pathway of apoptosis. However, the process by which LfcinB triggers mitochondria-dependent apoptosis is not well understood. Here, we show that LfcinB-induced apoptosis in Jurkat T-leukemia cells was preceded by LfcinB binding to, and progressive permeabilization of the cell membrane. Colloidal gold electron microscopy revealed that LfcinB entered the cytoplasm of Jurkat T-leukemia cells prior to the onset of mitochondrial depolarization. LfcinB was not internalized by endocytosis because endocytosis inhibitors did not prevent LfcinB-induced cytotoxicity. Furthermore, intracellular delivery of LfcinB via fusogenic liposomes caused the death of Jurkat T-leukemia cells, as well as normal human fibroblasts. Collectively, these findings suggest that LfcinB caused damage to the cell membrane that allowed LfcinB to enter the cytoplasm of Jurkat T-leukemia cells and mediate cytotoxicity. In addition, confocal microscopy showed that intracellular LfcinB co-localized with mitochondria in Jurkat T-leukemia cells, while flow cytometry and colloidal gold electron microscopy showed that LfcinB rapidly associated with purified mitochondria. Furthermore, purified mitochondria treated with LfcinB rapidly lost transmembrane potential and released cytochrome c. We conclude that LfcinB-induced apoptosis in Jurkat T-leukemia cells resulted from cell membrane damage and the subsequent disruption of mitochondrial membranes by internalized LfcinB.