Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos

Journal of Cell Death

Volumn 7, Issue , 2014, Pages 25-31

  Jewhurst, Kyle ^a   Levin, Michael ^a   McLaughlin, Kelly A ^a  

^a TUFTS UNIVERSITY   (United States)

Author keywords

Apoptosis; KillerRed; Optogenetics; Regeneration; Xenopus

Indexed keywords

KILLERRED PROTEIN; MESSENGER RNA; REACTIVE OXYGEN METABOLITE; RED FLUORESCENT PROTEIN; UNCLASSIFIED DRUG;

ADULT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; EMBRYO; FEMALE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MALE; NONHUMAN; OPTOGENETICS; PHOTOACTIVATION; PROTEIN EXPRESSION; XENOPUS LAEVIS;

EID: 84907873848     PISSN: None     EISSN: 11790660     Source Type: Journal    
DOI: 10.4137/JCD.S18368     Document Type: Article

References (30)

1. Deisseroth K. Optogenetics. Nat Methods. 2011;8(1):26–29.
2. Bulina ME, Chudakov DM, Britanova OV, et al. A genetically encoded photo­sensitizer. Nat Biotechnol. 2005;24(1):95–99.
3. Shu X, Lev-Ram V, Deerinck TJ, et al. A genetically encoded tag for correlated light and electron microscopy of intact cells, tissues, and organisms. PLoS Biol. 2011;9(4):e1001041.
4. Serebrovskaya EO, Edelweiss EF, Stremovskiy OA, Lukyanov KA, Chudakov DM, Deyev SM. Targeting cancer cells by using an antireceptor antibody-photosensitizer fusion protein. Proc Natl Acad Sci U S A. 2009;106(23):9221–9225.
5. Serebrovskaya EO, Gorodnicheva TV, Ermakova GV, et al. Light-induced blockage of cell division with a chromatin-targeted phototoxic fluorescent protein. Biochem J. 2011;435:65–71.
6. Shirmanova MV, Serebrovskaya EO, Snopova LB, et al. KillerRed and miniSOG as genetically encoded photosensitizers for photodynamic therapy of cancer. Proceedings of SPIE. May 12 2013; Munich, Germany. 2013;8803: 88030L1–88030L5.
7. Shirmanova MV, Serebrovskaya EO, Lukyanov KA, et al. Phototoxic effects of fluorescent protein KillerRed on tumor cells in mice. J Biophotonics. 2012;6: 283–290.
8. Glücksmann A. Cell deaths in normal vertebrate ontogeny. Biol Rev. 1951;26(1): 59–86.
9. Jacobson MD, Weil M, Raff MC. Programmed cell death in animal develop­ment. Cell. 1997;88(3):347–354.
10. Nishikawa A, Hayashi H. Spatial, temporal and hormonal regulation of pro­grammed muscle cell death during metamorphosis of the frog Xenopus laevis. Differentiation. 1995;59(4):207–214.
11. Hensey C, Gautier J. Programmed cell death during Xenopus development: a spatio-temporal analysis. Dev Biol. 1998;203(1):36–48.
12. Birnbaum KD, Alvarado AS. Slicing across kingdoms: regeneration in plants and animals. Cell. 2008;132(4):697–710.
13. Beck CW, Izpisúa Belmonte JC, Christen B. Beyond early development: Xeno­pus as an emerging model for the study of regenerative mechanisms. Dev Dyn. 2009;238(6):1226–1248.
14. Freeman G. Lens regeneration from the cornea in Xenopus laevis. J Exp Zool. 1963;154(1):39–65.
15. Vergara MN, Del Rio-Tsonis K. Retinal regeneration in the Xenopus laevis tad­pole: a new model system. Mol Vis. 2009;15:1000–1013.
16. Caine ST, McLaughlin KA. Regeneration of functional pronephric proximal tubules after partial nephrectomy in Xenopus laevis. Dev Dyn. 2013;3:219–229.
17. Tseng A, Adams DS, Qiu D, Koustubhan P, Levin M. Apoptosis is required dur­ing early stages of tail regeneration in Xenopus laevis. Dev Biol. 2007;301(1):62–69.
18. Dent JN. Limb regeneration in larvae and metamorphosing individuals of the South African clawed toad. J Morphol. 1962;110(1):61–77.
19. Hayakawa Y, Chandra M, Miao W, et al. Inhibition of cardiac myocyte apopto­sis improves cardiac function and abolishes mortality in the peripartum cardio­myopathy of gαq transgenic mice. Circulation. 2003;108(24):3036–3041.
20. Matsushita K, Iwanaga S, Oda T, et al. Interleukin-6/soluble interleukin-6 receptor complex reduces infarct size via inhibiting myocardial apoptosis. Lab Invest. 2005;85(10):1210–1223.
21. Palojoki E, Saraste A, Eriksson A, et al. Cardiomyocyte apoptosis and ven­tricular remodeling after myocardial infarction in rats. Am J Physiol—Heart Circ Physiol. 2001;280(6):2726–2731.
22. Bernard L. Reactive oxygen species in photochemistry of the red fluorescent pro­tein “Killer red”. Chem Commun. 2011;47(17):4887–4889.
23. Bulina ME, Lukyanov KA, Britanova OV, Onichtchouk D, Lukyanov S, Chudakov DM. Chromophore-assisted light inactivation (CALI) using the phototoxic fluorescent protein KillerRed. Nat Protoc. 2006;1(2):947–953.
24. Waldeck W, Mueller G, Wiessler M, Tóth K, Braun K. Positioning effects of KillerRed inside of cells correlate with DNA strand breaks after activation with visible light. Int J Med Sci. 2011;8(2):97.
25. Shibuya T, Tsujimoto Y. Deleterious effects of mitochondrial ROS generated by KillerRed photodynamic action in human cell lines and C. elegans. J Photochem Photobiol B: Biol. 2012;117:1–12.
26. Teh C, Chudakov DM, Poon KL, et al. Optogenetic in vivo cell manipulation in KillerRed-expressing zebrafish transgenics. BMC Dev Biol. 2010;10(1):110.
27. Nieuwkoop PD, Faber J. Normal table of Xenopus laevis (daudin). Amsterdam: North Holland Publishing Company; 1967.
28. Moody SA, Kline MJ. Segregation of fate during cleavage of frog (Xenopus lae­vis) blastomeres. Anat Embryol. 1990;182(4):347–362.
29. Owusu-Ansah E, Yavari A, Banerjee U. A protocol for in vivo detection of reac­tive oxygen species. Protoc Exchange. 2008. doi:10.1038/nprot.2008.23.
30. Qi YB, Garren EJ, Shu X, Tsien RY, Jin Y. Photo-inducible cell ablation in Caenorhabditis elegans using the genetically encoded singlet oxygen generating protein miniSOG. Proc Natl Acad Sci U S A. 2012;109(19):7499–7504