TY - JOUR
T1 - The cytotoxic and hemolytic potential of karmitoxin from Karlodinium armiger and how it interacts with sterols
AU - Prause, Hélène-Christine
AU - Hochmayr, Nadine
AU - Yu, Yanan
AU - Larsen, Thomas Ostenfeld
AU - Hansen, Per Juel
AU - Del Favero, Giorgia
AU - Marko, Doris
AU - Place, Allen
AU - Varga, Elisabeth
PY - 2025
Y1 - 2025
N2 - Karmitoxin, produced by Karlodinium armiger, is structurally related to karlotoxin and amphidinols, two potent ichthyotoxic hemolysins with high affinity for sterols. Given these structural similarities, karmitoxin is believed to exhibit comparable toxic effects. Cytotoxicity was assessed in the fish gill cell line RTgill-W1 and the human epithelial colon cell line HCEC-1CT. The hemolytic potential with and without added sterols was tested on fish erythrocytes to investigate possible impacts of toxin-sterol interactions. Sterol interactions were further evaluated using surface plasmon resonance. A 3-h incubation returned an EC50 of 111 and 175 nM in RTgill-W1 and in HCEC-1CT cells, respectively. Lactate dehydrogenase (LDH) release increased with toxin concentration, reaching 11 % in the fish and 40 % in the human cell line. Extended exposure (24 h) increased the toxicity in RTgill-W1 cells (EC50 74 nM, 40 % LDH release). In parallel, hemolytic potential of karmitoxin was confirmed, as well as its interaction with free sterols. Interaction kinetics revealed complex stabilities with kd(s−1) constants of 1.13 × 10−2 (cholesterol), 5.48 × 10−3 (epicholesterol), and 4.72 × 10−3 (ergosterol). Interaction with cholesterol followed the single-exponential model well, while data indicated more complex binding with epicholesterol and ergosterol. Altering the RTgill-W1 cholesterol content did not impact cytotoxicity at the tested concentration. Overall, karmitoxin showed potent cytotoxic and hemolytic properties in human and fish models. Complex formation with sterols may play a role in membrane targeting, yet cellular cholesterol quantity might not affect cytotoxicity.
AB - Karmitoxin, produced by Karlodinium armiger, is structurally related to karlotoxin and amphidinols, two potent ichthyotoxic hemolysins with high affinity for sterols. Given these structural similarities, karmitoxin is believed to exhibit comparable toxic effects. Cytotoxicity was assessed in the fish gill cell line RTgill-W1 and the human epithelial colon cell line HCEC-1CT. The hemolytic potential with and without added sterols was tested on fish erythrocytes to investigate possible impacts of toxin-sterol interactions. Sterol interactions were further evaluated using surface plasmon resonance. A 3-h incubation returned an EC50 of 111 and 175 nM in RTgill-W1 and in HCEC-1CT cells, respectively. Lactate dehydrogenase (LDH) release increased with toxin concentration, reaching 11 % in the fish and 40 % in the human cell line. Extended exposure (24 h) increased the toxicity in RTgill-W1 cells (EC50 74 nM, 40 % LDH release). In parallel, hemolytic potential of karmitoxin was confirmed, as well as its interaction with free sterols. Interaction kinetics revealed complex stabilities with kd(s−1) constants of 1.13 × 10−2 (cholesterol), 5.48 × 10−3 (epicholesterol), and 4.72 × 10−3 (ergosterol). Interaction with cholesterol followed the single-exponential model well, while data indicated more complex binding with epicholesterol and ergosterol. Altering the RTgill-W1 cholesterol content did not impact cytotoxicity at the tested concentration. Overall, karmitoxin showed potent cytotoxic and hemolytic properties in human and fish models. Complex formation with sterols may play a role in membrane targeting, yet cellular cholesterol quantity might not affect cytotoxicity.
KW - Ichthyotoxin
KW - Mode of action
KW - Lysis
KW - Cholesterol
KW - RTgill-W1
KW - HCEC-1CT
U2 - 10.1016/j.hal.2025.102817
DO - 10.1016/j.hal.2025.102817
M3 - Journal article
SN - 1568-9883
VL - 143
JO - Harmful Algae
JF - Harmful Algae
M1 - 102817
ER -