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Toxicity and Side Effects of Cell-Penetrating Peptides 259
6. Boman, H.G., Gene-encoded peptide antibiotics and the concept of innate immunity:
an update review, Scand. J. Immunol., 48, 15, 1998.
7. Dathe, M. and Wieprecht, T., Structural features of helical antimicrobial peptides:
their potential to modulate activity on model membranes and biological cells, Biochim.
Biophys. Acta, 1462, 71, 1999.
8. Oehlke, J. et al., Cellular uptake of an alpha-helical amphipathic model peptide with
the potential to deliver polar compounds into the cell interior nonendocytically,
Biochim. Biophys. Acta, 1414, 127, 1998.
9. Derossi, D. et al., Cell internalization of the third helix of the Antennapedia homeodomain
is receptor-independent. J. Biol. Chem., 271, 18188, 1996.
10. Du, C. et al., Conformational and topological requirements of cell-permeable peptide
function, J. Pept. Res., 51, 235, 1998.
11. Oehlke, J. et al., Extensive cellular uptake into endothelial cells of an amphipathic
beta-sheet forming peptide, FEBS Lett., 415, 196, 1997.
12. Acosta, D. et al., An in vitro approach to the study of target organ toxicity of drugs
and chemicals, In Vitro Cell Dev. Biol., 21, 495, 1985.
13. Kaltenback, J.P., Kaltenback, M.H., and Lyons, W.B., Nigrosin as a dye for differentiating
live and dead ascites cells, Exp. Cell Res., 15, 112, 1958.
14. Hällbrink, M. et al., Quantification of cellular uptake and comparison of some cell
penetrating peptides, Biochim. Biophys. Acta, 1515, 101, 2001.
15. Melamed, M.R., Kamentsky, L.A., and Boyse, E.A., Cytotoxic test automation: a
live-dead cell differential counter, Science, 163, 285, 1969.
16. Walum, E., Peterson, A., and Erkell, L.J., Photometric recording of cell viability using
trypan blue in perfused cell cultures, Xenobiotica, 15, 701, 1985.
17. Saijo, N., A spectrophotometric quantitation of cytotoxic action of antiserum and
complement by trypan blue, Immunology, 24, 683, 1973.
18. Jones, K.H. and Senft, J.A., An improved method to determine cell viability by
simultaneous staining with fluorescein diacetate-propidium iodide, J. Histochem.
Cytochem., 33, 77, 1985.
19. Juurlink, B.H. and Hertz, L., Ischemia-induced death of astrocytes and neurons in
primary culture: pitfalls in quantifying neuronal cell death, Brain Res. Dev. Brain
Res., 71, 239, 1993.
20. Scheller, A. et al., Evidence for an amphipathicity independent cellular uptake of
amphipathic cell-penetrating peptides, Eur. J. Biochem., 267, 6043, 2000.
21. Wender, P.A. et al., The design, synthesis, and evaluation of molecules that enable
or enhance cellular uptake: peptoid molecular transporters, Proc. Natl. Acad. Sci.
U.S.A., 97, 13003, 2000.
22. Walum, E. and Peterson, A., Tritiated 2-deoxy-D-glucose as a probe for cell membrane
permeability studies, Anal. Biochem., 120, 8, 1982.
23. Mitchell, D.B. and Acosta, D., Evaluation of the cytotoxicity of tricyclic antidepressants
in primary cultures of rat hepatocytes, J. Toxicol. Environ. Health, 7, 83, 1981.
24. Thelestam, M. and Mollby, R., Cytotoxic effects on the plasma membrane of human
diploid fibroblasts — a comparative study of leakage tests, Med. Biol., 54, 39, 1976.
25. Zawydiwski, R. and Duncan, R., Spontaneous 51Cr release by isolated rat hepatocytes:
an indicator of membrane damage, In Vitro, 14, 707, 1978.
26. Smith, D.E. and Gorski, J., Extrogen control of uterine glucose metabolism. An
analysis based on the transport and phosphorylation of 2-deoxyglucose, J. Biol.
Chem., 243, 4169, 1968.