In vivo labeling of peroxisomes by photoconvertible mEos2 in myelinating glia of mice

Biochimie

Volumn 98, Issue 1, 2014, Pages 127-134

  Richert, Sarah ^a   Kleinecke, Sandra ^a   Günther, Jenniffer ^a   Schaumburg, Florian ^a   Edgar, Julia ^a   Nienhaus, Gerd Ulrich ^b   Nave, Klaus Armin ^a   Kassmann, Celia M ^a  

^a MAX PLANCK INSTITUTE OF EXPERIMENTAL MEDICINE   (Germany)

^b KARLSRUHE INSTITUTE OF TECHNOLOGY   (Germany)

Author keywords

Fluorescent peroxisomes; mEos2; Oligodendrocytes; Photoconversion; Transgenic mouse

Indexed keywords

2',3' CYCLIC NUCLEOTIDE 3' PHOSPHODIESTERASE; LYSOSOME ASSOCIATED MEMBRANE PROTEIN 1; MEOS2 PROTEIN; MYELIN; MYELIN PROTEIN; OLIGODENDROCYTE TRANSCRIPTION FACTOR 2; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ANTERIOR COMMISSURE; ASTROCYTE; BRAIN STEM; CELL LABELING; CONFOCAL LASER SCANNING MICROSCOPE; CORPUS CALLOSUM; CYTOPLASM; FRONTAL CORTEX; FUSION GENE; GLIA; IN VIVO STUDY; MITOCHONDRIAL TARGETING SIGNAL; MOUSE; MYELINATED NERVE; MYELINATION; NICK END LABELING; NONHUMAN; OLIGODENDROGLIA; PEROXISOMAL TARGETING SIGNAL; PEROXISOME; POLYMERASE CHAIN REACTION; PROMOTER REGION; PROTEIN EXPRESSION; RESTRICTION SITE; REVIEW; SCIATIC NERVE; SIGNAL TRANSDUCTION; SPINAL CORD; START CODON; TRANSGENIC MOUSE; WHITE MATTER;

MUS; MUS MUSCULUS;

FLUORESCENT PEROXISOMES; MEOS2; OLIGODENDROCYTES; PHOTOCONVERSION; TRANSGENIC MOUSE;

ANIMALS; MICE; MICE, TRANSGENIC; MYELIN SHEATH; NEUROGLIA; OLIGODENDROGLIA; PEROXISOMES;

EID: 84895082557     PISSN: 03009084     EISSN: 61831638     Source Type: Journal    
DOI: 10.1016/j.biochi.2013.10.022     Document Type: Article

References (44)

1. R.J.A. Wanders, and H.R. Waterham Biochemistry of mammalian peroxisomes revisited Annu. Rev. Biochem. 75 2006 295 332
2. M. Fransen Peroxisome dynamics: molecular players, mechanisms, and (Dys)functions ISRN Cell Biol. 2012 2012 1 24
3. K. Zaar, H.-P. Köst, A. Schad, A. Völkl, E. Baumgart, and H.D. Fahimi Cellular and subcellular distribution of D-aspartate oxidase in human and rat brain J. Comp. Neurol. 450 2002 272 282
4. B. Ahlemeyer, I. Neubert, W.J. Kovacs, and E. Baumgart-Vogt Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain J. Comp. Neurol. 505 2007 1 17
5. N.E. Braverman, M.D. D'Agostino, and G.E. MacLean Peroxisome biogenesis disorders: Biological, clinical and pathophysiological perspectives Dev. Disabil. Res. Rev. 17 2013 187 196
6. S.J.S. Gould, G.A.G. Keller, N.N. Hosken, J.J. Wilkinson, and S.S. Subramani A conserved tripeptide sorts proteins to peroxisomes J. Cell Biol. 108 1989 1657 1664
7. H.J. Kim, I.S. Woo, E.S. Kang, S.Y. Eun, H.J. Kim, and J.H. Lee et al. Identification of a truncated alternative splicing variant of human PPARgamma1 that exhibits dominant negative activity Biochem. Biophys. Res. Commun. 347 2006 698 706
8. O. Ivashchenko, P.P. Van Veldhoven, C. Brees, Ye-Shih Ho, S.R. Terlecky, and M. Fransen Intraperoxisomal redox balance in mammalian cells: oxidative stress and interorganellar cross-talk Mol. Biol. Cell 22 2011 1440 1451
9. S. Kredel, F. Oswald, K. Nienhaus, K. Deuschle, C. Röcker, and M. Wolff et al. mRuby, a bright monomeric red fluorescent protein for labeling of subcellular structures PLoS One 4 2009 e4391
10. C.Y. Fan, J. Pan, R. Chu, D. Lee, K.D. Kluckman, and N. Usuda et al. Targeted disruption of the peroxisomal fatty acyl-CoA oxidase gene: generation of a mouse model of pseudoneonatal adrenoleukodystrophy Ann. N. Y. Acad. Sci. 804 1996 530 541
11. M. Baes, P. Gressens, E. Baumgart, P. Carmeliet, M. Casteels, and M. Fransen et al. A mouse model for Zellweger syndrome Nat. Genet. 17 1997 49 57
12. P.L. Faust, and M.E. Hatten Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder J. Cell Biol. 139 1997 1293 1305
13. S. Forss-Petter, H. Werner, J. Berger, H. Lassmann, B. Molzer, and M.H. Schwab et al. Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice J. Neurosci. Res. 50 1997 829 843
14. Kobayashi, N. Shinnoh, A. Kondo, and T. Yamada Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism Biochem. Biophys. Res. Commun. 232 1997 631 636
15. J.F. Lu, A.M. Lawler, P.A. Watkins, J.M. Powers, A.B. Moser, and H.W. Moser et al. A mouse model for X-linked adrenoleukodystrophy Proc. Natl. Acad. Sci. U. S. A. 94 1997 9366 9371
16. P. Brites, A.M. Motley, P. Gressens, P.A.W. Mooyer, I. Ploegaert, and V. Everts et al. Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata Hum. Mol. Genet. 12 2003 2255 2267
17. Y.-S. Ho, Y. Xiong, W. Ma, A. Spector, and D.S. Ho Mice lacking catalase develop normally but show differential sensitivity to oxidant tissue injury J. Biol. Chem. 279 2004 32804 32812
18. G. Chevillard, M.-C. Clémencet, N. Latruffe, and V. Nicolas-Francès Targeted disruption of the peroxisomal thiolase B gene in mouse: a new model to study disorders related to peroxisomal lipid metabolism Biochimie 86 2004 849 856
19. S. Ferdinandusse, S. Denis, H. Overmars, L. Van Eeckhoudt, P.P. Van Veldhoven, and M. Duran et al. Developmental changes of bile acid composition and conjugation in L- and D-bifunctional protein single and double knockout mice J. Biol. Chem. 280 2005 18658 18666
20. I. Ferrer, J.P. Kapfhammer, C. Hindelang, S. Kemp, N. Troffer-Charlier, and V. Broccoli et al. Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage Hum. Mol. Genet. 14 2005 3565 3577
21. A. Teigler, D. Komljenovic, A. Draguhn, K. Gorgas, and W.W. Just Defects in myelination, paranode organization and Purkinje cell innervation in the ether lipid-deficient mouse cerebellum Hum. Mol. Genet. 18 2009 1897 1908
22. C.M. Kassmann, C. Lappe-Siefke, M. Baes, B. Brügger, A. Mildner, and H.B. Werner et al. Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes Nat. Genet. 39 2007 969 976
23. L. Hulshagen, O. Krysko, A. Bottelbergs, S. Huyghe, R. Klein, and P.P. Van Veldhoven et al. Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration J. Neurosci. 28 2008 4015 4027
24. A. Bottelbergs, S. Verheijden, L. Hulshagen, D.H. Gutmann, S. Goebbels, and K.-A. Nave et al. Axonal integrity in the absence of functional peroxisomes from projection neurons and astrocytes Glia 58 2010 1532 1543
25. C. Lappe-Siefke, S. Goebbels, M. Gravel, E. Nicksch, J. Lee, and P.E. Braun et al. Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination Nat. Genet. 33 2003 366 374
26. J. Wiedenmann EosFP, a fluorescent marker protein with UV-inducible green-to-red fluorescence conversion Proc. Natl. Acad. Sci. U. S. A. 101 2004 15905 15910
27. S.A. McKinney, C.S. Murphy, K.L. Hazelwood, M.W. Davidson, and L.L. Looger A bright and photostable photoconvertible fluorescent protein Nat. Meth. 6 2009 131 133
28. M. Gravel, A. Di Polo, P.B. Valera, and P.E. Braun Four-kilobase sequence of the mouse CNP gene directs spatial and temporal expression of lacZ in transgenic mice J. Neurosci. Res. 53 1998 393 404
29. K.L. Ligon, J.A. Alberta, A.T. Kho, J. Weiss, M.R. Kwaan, and C.L. Nutt et al. The oligodendroglial lineage marker OLIG2 is universally expressed in diffuse gliomas J. Neuropathol. Exp. Neurol. 63 2004 499 509
30. M. Jung, E. Krämer, M. Grzenkowski, K. Tang, W. Blakemore, and A. Aguzzi et al. Lines of murine oligodendroglial precursor cells immortalized by an activated neu tyrosine kinase show distinct degrees of interaction with axons in vitro and in vivo Eur. J. Neurosci. 7 1995 1245 1265
31. C. Klein, E.-M. Kramer, A.-M. Cardine, B. Schraven, R. Brandt, and J. Trotter Process outgrowth of oligodendrocytes is promoted by interaction of fyn kinase with the cytoskeletal protein tau J. Neurosci. 22 2002 698 707
32. J. Xu Preparation, Culture, and Immortalization of Mouse Embryonic Fibroblasts 2001 John Wiley & Sons, Inc Hoboken, NJ, USA
33. J. Lee, R.C. O'Neill, M.W. Park, M. Gravel, and P.E. Braun Mitochondrial localization of CNP2 is regulated by phosphorylation of the N-terminal targeting signal by PKC: implications of a mitochondrial function for CNP2 in glial and non-glial cells Mol. Cell. Neurosci. 31 2006 446 462
34. W.-P. Yu, E.J. Coliarini, N.P. Pringle, and W.D. Richardson Embryonic expression of myelin genes: evidence for a focal source of oligodendrocyte precursors in the ventricular zone of the neural tube Neuron 12 1994 1353 1362
35. C.M. Kassmann, S. Quintes, J. Rietdorf, W. Möbius, M.W. Sereda, and T. Nientiedt et al. A role for myelin-associated peroxisomes in maintaining paranodal loops and axonal integrity FEBS Lett. 585 2011 2205 2211
36. T.J. Sprinkle, F.A. McMorris, J. Yoshino, and G.H. DeVries Differential expression of 2′:3′-cyclic nucleotide 3′-phosphodiesterase in cultured central, peripheral, and extraneural cells Neurochem. Res. 10 1985 919 931
37. S. Weissbarth, H.S. Maker, I. Raes, T.S. Brannan, E.P. Lapin, and G.M. Lehrer The activity of 2′,3′-cyclic nucleotide 3′- phosphodiesterase in rat tissues J. Neurochem. 37 1981 677 680
38. M.S. Davidoff, R. Middendorff, E. Köfüncü, D. Müller, D. Jezek, and A.F. Holstein Leydig cells of the human testis possess astrocyte and oligodendrocyte marker molecules Acta Histochem. 104 2002 39 49
39. T.B. Dansen, K.W. Wirtz, R.J. Wanders, and E.H. Pap Peroxisomes in human fibroblasts have a basic pH Nat. Cell Biol. 2 2000 51 53
40. M. Kneen, J. Farinas, Y. Li, and A.S. Verkman Green fluorescent protein as a noninvasive intracellular pH indicator Biophysical. J. 74 1998 1591 1599
41. S. Belachew, X. Yuan, and V. Gallo Unraveling oligodendrocyte origin and function by cell-specific transgenesis Dev. Neurosci. 23 2001 287 298
42. M. Schrader, and H.D. Fahimi Growth and division of peroxisomes Int. Rev. Cytol. 255 2006 237 290
43. M. Schrader, N.A. Bonekamp, and M. Islinger Fission and proliferation of peroxisomes Biochim. Biophys. Acta 1822 2012 1343 1357
44. I. Singh, and A. Pujol Pathomechanisms underlying X-adrenoleukodystrophy: a three-hit hypothesis Brain Pathol. 20 2010 838 844.s