참고문헌
- Ramon y Cajal, S. (1995) Histology of the Nervous System of Man and Vertebrates, Oxford University Press, New York, USA.
- Scheibel, M. E., Lindsay, R. D., Tomiyasu, U. and Scheibel, A. B. (1975) Progressive dendritic changes in aging human cortex. Exp. Neurol. 47, 392-403 https://doi.org/10.1016/0014-4886(75)90072-2
- Buell, S. J. and Coleman, P. D. (1979) Dendritic growth in the aged human brain and failure of growth in senile dementia. Science 206, 854-856 https://doi.org/10.1126/science.493989
- Arendt, T., Schindler, C., Bruckner, M. K., Eschrich, K., Bigl, V., Zedlick, D. and Marcova, L. (1997) Plastic neuronal remodeling is impaired in patients with Alzheimer's disease carrying apolipoprotein e4 allele. J. Neurosci. 17, 516-529 https://doi.org/10.1523/JNEUROSCI.17-02-00516.1997
- Mesulam, M.M. (1999) Neuroplasticity failure in Alzheimer's disease: bridging the gap between plaques and tangles. Neuron 24, 521-529 https://doi.org/10.1016/S0896-6273(00)81109-5
- Mehraein, P., Yamada, M. and Tarnowska-Dziduszko, E. (1975) Quantitative study on dendrites and dendritic spines in Alzheimer's disease and senile dementia. Adv. Neurol. 12, 453-458
- Paula-Barbosa, M. M., Mota Cardoso, R., Faria, R. and Cruz, C. (1978) Multivesicular bodies in cortical dendrites of two patients with Alzheimer's disease. J. Neurol. Sci. 36, 259-264 https://doi.org/10.1016/0022-510X(78)90086-2
- Arendt, T., Zvegintseva, H. G. and Leontovich, T. A. (1986) Dendritic changes in the basal nucleus of Meynert and in the diagonal band nucleus in Alzheimer's disease- A quantitative Golgi investigation. Neuroscience 19, 1265-1278 https://doi.org/10.1016/0306-4522(86)90141-7
- M. and Terry, R. (1994) Synaptic and neuritic alterations during the progression of Alzheimer's disease. Neurosci. Lett. 174, 67-72 https://doi.org/10.1016/0304-3940(94)90121-X
- de Ruiter, J. P. and Uylings, H. B. M. (1987) Morphometric and dendritic analysis of fascia dentata granule cells in human aging and senile dementia. Brain Res. 402, 217-229 https://doi.org/10.1016/0006-8993(87)90028-X
- Mucke, L., Masliah, E., Yu, G. Q., Mallory, M., Rockenstein, E. M., Tatsuno, G., Hu, K., Kholodenko, D., Johnson-Wood, K. and McConlogue, L. (2000) High-level neuronal expression of abeta 1-42 in wild-type human amyloid protein precursor transgenic mice: synaptotoxicity without plaque formation. J. Neurosci. 20, 4050- 4058 https://doi.org/10.1523/JNEUROSCI.20-11-04050.2000
- Wu, C. C., Chawla, F., Games, D., Rydel, R. E., Freedman, S., Schenk, D., Young, W. G., Morrison, J. H. and Bloom, F. E. (2004) Selective vulnerability of dentate granule cells prior to amyloid deposition in PDAPP mice: digital morphometric analyses. Proc. Natl. Acad. Sci. U.S.A. 101, 7141-7146
- Odorizzi, G., Babst M. and Emr, S.D. (1998) Fab1p PtdIns(3)P 5-kinase function essential for protein sorting in the multivesicular body. Cell 95, 847-858 https://doi.org/10.1016/S0092-8674(00)81707-9
- Katzmann, D.J., Babst, M. and Emr, S.D. (2001) Ubiquitin-dependent sorting into the multivesicular body pathway requires the function of a conserved endosomal protein sorting complex, ESCRT-I. Cell 106, 145-155 https://doi.org/10.1016/S0092-8674(01)00434-2
- Babst, M., Katzmann, D.J., Snyder, W.B., Wendland, B. and Emr, S.D. (2002) Endosome-associated complex, ESCRT-II, recruits transport machinery for protein sorting at the multivesicular body. Dev. Cell 3, 283-289 https://doi.org/10.1016/S1534-5807(02)00219-8
- Babst, M., Katzmann, D.J., Estepa-Sabal, E.J., Meerloo, T. and Emr, S.D. (2002) Escrt-III: an endosome-associated heterooligomeric protein complex required for MVB sorting. Dev. Cell 3, 271-282 https://doi.org/10.1016/S1534-5807(02)00220-4
- Chu, T., Sun, J., Saksena, S. and Emr, S. D. (2006) New component of ESCRT-I regulates endosomal sorting complex assembly. J. Cell Biol. 175, 815-823 https://doi.org/10.1083/jcb.200608053
- Bache, K. G., Brech, A., Mehlum, A. and Stenmark, H. (2003) Hrs regulates multivesicular body formation via ESCRT recruitment to endosomes. J. Cell Biol. 162, 435- 442 https://doi.org/10.1083/jcb.200302131
- Katzmann, D. J., Stefan, C. J., Babst, M. and Emr, S. D. (2003) Vps27 recruits ESCRT machinery to endosomes during MVB sorting. J. Cell Biol. 162, 413-423 https://doi.org/10.1083/jcb.200302136
- Nickerson, D. P., Russell, M. R. and Odorizzi, G. (2007) A concentric circle model of multivesicular body cargo sorting. EMBO Rep. 8, 644-650 https://doi.org/10.1038/sj.embor.7401004
- Hurley, J. H. (2008) ESCRT complexes and the biogenesis of multivesicular bodies. Curr. Opin. Cell Biol. 20, 4-11 https://doi.org/10.1016/j.ceb.2007.12.002
- Howard, T. L., Stauffer, D. R., Degnin, C. R. and Hollenberg, S. M. (2001) CHMP1 functions as a member of a newly defined family of vesicle trafficking proteins. J. Cell Sci. 114, 2395-2404
- Obita, T., Saksena, S., Ghazi-Tabatabai, S., Gill, D.J., Perisic, O., Emr, S.D. and Williams, R. L. (2007) Structural basis for selective recognition of ESCRT-III by the AAA ATPase Vps4. Nature 449, 735-739 https://doi.org/10.1038/nature06171
- Stuchell-Brereton, M. D., Skalicky, J. J., Kieffer, C., Karren, M. A., Ghaffarian, S., Sundquist, W. I. (2007) ESCRT-III recognition by VPS4 ATPases. Nature 449, 740-744 https://doi.org/10.1038/nature06172
- Strack, B., Calistri, A., Craig, S., Popova, E. and Gottlinger, H. G. (2003) AIP1/ALIX is a binding partner for HIV-1 p6 and EIAV p9 functioning in virus budding. Cell 114, 689-699 https://doi.org/10.1016/S0092-8674(03)00653-6
- von Schwedler, U. K., Stuchell, M., Muller, B., Ward, D. M., Chung, H. Y., Morita, E., Wang, H. E., Davis, T., He, G. P., Cimbora, D. M., et al. (2003) The protein network of HIV budding. Cell 114, 701-713 https://doi.org/10.1016/S0092-8674(03)00714-1
- Carlton, J. G., Agromayor, M., Martin-Serrano, J. (2008) Differential requirements for Alix and ESCRT-III in cytokinesis and HIV-1 release. Proc. Natl. Acad. Sci. USA 105, 10541-10546
- Carlton, J. G., Martin-Serrano, J. (2007) Parallels between cytokinesis and retroviral budding: a role for the ESCRT machinery. Science 316, 1908-1912 https://doi.org/10.1126/science.1143422
- Irion, U. and St Johnston, D. (2007) Linksbicoid RNA localization localization requires specific binding of an endosomal sorting complex. Nature 445, 554-558 https://doi.org/10.1038/nature05503
- Kamura, T., Burian, D., Khalili, H., Schmidt, S. L., Sato, S., Liu, W. J., Conrad, M. N., Conaway, R. C., Conaway, J. W. and Shilatifard, A. J. (2001) Cloning and characterization of ELL-associated proteins EAP45 and EAP20. A role for yeast EAP-like proteins in regulation of gene expression by glucose. Biol. Chem. 276, 16528-16533 https://doi.org/10.1074/jbc.M010142200
- Stauffer, D. R., Howard, T. L., Nyun, T. and Hollenberg, S. M. (2001) CHMP1 is a novel nuclear matrix protein affecting chromatin structure and cell-cycle progression. J. Cell Sci. 114, 2383-2393
- Thompson, B. J., Mathieu, J., Sung, H. H., Loeser, E., Rorth, P. and Cohen, S. M. (2005) Tumor suppressor properties of the ESCRT-II complex component Vps25 in Drosophila. Dev. Cell. 9, 711-720 https://doi.org/10.1016/j.devcel.2005.09.020
- Vaccari, T. and Bilder, D. (2005) The Drosophila tumor suppressor vps25 prevents nonautonomous overproliferation by regulating notch trafficking. Dev. Cell 9, 687-698 https://doi.org/10.1016/j.devcel.2005.09.019
- Moberg, K. H., Schelble, S., Burdick, S. K. and Hariharan, I. K. (2005) Mutations in erupted, the Drosophila ortholog of mammaliantumor susceptibility gene 101, elicit non-cell-autonomous overgrowth. Dev. Cell 9, 699-710 https://doi.org/10.1016/j.devcel.2005.09.018
- Sweeney, N. T., Brenman, J. E., Jan, Y. N. and Gao, F. B. (2006) The coiled-coil protein Shrub controls neuronal morphogenesis in Drosophila. Curr. Biol. 16,1006-1011 https://doi.org/10.1016/j.cub.2006.03.067
- Lee, J. A., Beigneux, A., Ahmad, S. T., Young, S. G. and Gao, F. B. (2007) ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration. Curr. Biol. 17, 1561-1567 https://doi.org/10.1016/j.cub.2007.07.029
- Mizushima, N., Levine, B., Cuervo, A. M. and Klionsky, D. J. (2008) Autophagy fights disease through cellular self-digestion. Nature 451, 1069-1075 https://doi.org/10.1038/nature06639
- Tooze, J., Hollinshead, M., Ludwig, T., Howell, K., Hoflack, B. and Kern, H. (1990) In exocrine pancreas, the basolateral endocytic pathway converges with the autophagic pathway immediately after the early endosome. J. Cell Biol. 111, 329-345 https://doi.org/10.1083/jcb.111.2.329
- Liou, W., Geuze, H. J., Geelen, M. J. and Slot, J. W. (1997) The autophagic and endocytic pathways converge at the nascent autophagic vacuoles. J. Cell Biol. 136, 61-70 https://doi.org/10.1083/jcb.136.1.61
- Berg, T. O., Fengsrud, M., Stromhaug, P. E., Berg, T. and Seglen, P. O. (1998) Isolation and characterization of rat liver amphisomes. Evidence for fusion of autophagosomes with both early and late endosomes. J. Biol. Chem. 273, 21883-21892 https://doi.org/10.1074/jbc.273.34.21883
- Lucocq, J. and Walker, D. (1997) Evidence for fusion between multilamellar endosomes and autophagosomes in HeLa cells. Eur. J. Cell Biol. 72, 307-313
- Kuma, A., Matsui, M. and Mizushima, N. (2007) LC3, an autophagosome marker, can be incorporated into protein aggregates independent of autophagy: caution in the interpretation of LC3 localization. Autophagy 3, 323-328 https://doi.org/10.4161/auto.4012
- Lee, J. A. and Gao, F. B. (2008) Roles of ESCRT in autophagy- associated neurodegeneration. Autophagy 4, 230-232 https://doi.org/10.4161/auto.5384
- Filimonenko, M., Stuffers, S., Raiborg, C., Yamamoto, A., Malerod, L., Fisher, E. M., Isaacs, A., Brech, A., Stenmark, H. and Simonsen, A. (2007) Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease. J. Cell Biol. 179, 485-500 https://doi.org/10.1083/jcb.200702115
- Komatsu, M., Waguri, S., Chiba, T., Murata, S., Iwata, J., Tanida, I., Ueno, T., Koike, M., Uchiyama, Y., Kominami, E., et al. (2006) Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature 441, 880-884 https://doi.org/10.1038/nature04723
- Hara, T., Nakamura, K., Matsui, M., Yamamoto, A., Nakahara, Y., Suzuki-Migishima, R., Yokoyama, M., Mishima, K., Saito, I., Okano, H., et al. (2006) Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice. Nature 441, 885-889 https://doi.org/10.1038/nature04724
- Boxer, A. L. and Miller, B. L. (2005) Clinical features of frontotemporal dementia. Alzheimer Dis. Assoc. Disord. 19(Suppl. 1), S3-6 https://doi.org/10.1097/01.wad.0000183086.99691.91
- Watts, G. D., Wymer, J., Kovach, M. J., Mehta, S. G., Mumm, S., Darvish, D., Pestronk, A., Whyte, M. P. and Kimonis, V. E. (2004) Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat. Genet. 36, 377-381 https://doi.org/10.1038/ng1332
- Baker, M. et al. (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442, 916-919 https://doi.org/10.1038/nature05016
- Cruts, M. et al. (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442, 920-924 https://doi.org/10.1038/nature05017
- Neumann, M., Sampathu, D. M., Kwong, L. K., Truax, A. C., Micsenyi, M. C., Chou, T. T., Bruce, J., Schuck, T., Grossman, M., Clark, C. M., McCluskey, L. F., Miller, B. L., Masliah, E., Mackenzie, I. R., Feldman, H., Feiden, W., Kretzschmar, H. A., Trojanowski, J. Q. and Lee, V. M. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130-133 https://doi.org/10.1126/science.1134108
- Arai, T., Hasegawa, M., Akiyama, H., Ikeda, K., Nonaka, T., Mori, H., Mann, D., Tsuchiya, K., Yoshida, M., Hashizume, Y. and Oda, T. (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem. Biophys. Res. Commun. 351, 602-611 https://doi.org/10.1016/j.bbrc.2006.10.093
- Skibinski, G., Parkinson, N. J., Brown, J. M., Chakrabarti, L., Lloyd, S. L., Hummerich, H., Nielsen. J. E., Hodges, J. R., et al. (2005) Mutations in the endosomal ESCRTIIIcomplex subunit CHMP2B in frontotemporal dementia. Nat. Genet. 37, 806-808 https://doi.org/10.1038/ng1609
- Momeni P, Bell J, Duckworth J, Hutton M, Mann D, Brown SP, Hardy J. (2006) Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B. Neurosci. Lett. 410, 77-79 https://doi.org/10.1016/j.neulet.2006.06.065
- Lindquist, S. G., Braedgaard, H., Svenstrup, K., Isaacs, A. M., Nielsen, J. E.; FReJA Consortium. (2008) Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family. Eur. J. Neurol. 15, 667-670 https://doi.org/10.1111/j.1468-1331.2008.02144.x
- van der Zee, J., Urwin, H., Engelborghs, S., Bruyland, M., Vandenberghe, R,. Dermaut, B., De Pooter, T., Peeters, K., Santens, P., De Deyn, P. P., Fisher, E. M., Collinge, J., Isaacs, A. M. and Van Broeckhoven, C. (2008) CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro. Hum. Mol. Genet. 17, 313-322 https://doi.org/10.1093/hmg/ddm309
- Momeni, P., Rogaeva, E., Van Deerlin, V., Yuan, W., Grafman, J., Tierney, M., Huey, E., Bell, J., Morris, C. M., Kalaria, R. N., van Rensburg, S. J., Niehaus, D., Potocnik, F., Kawarai, T., Salehi-Rad, S., Sato, C., St George-Hyslop, P. and Hardy, J. (2006) Genetic variability in CHMP2B and frontotemporal dementia. Neurodegener. Dis. 3, 129- 133 https://doi.org/10.1159/000094771
- Obita, T., Saksena, S., Ghazi-Tabatabai, S., Gill, D. J., Perisic, O., Emr, S. D. and Williams, R. L. (2007) Structural basis for selective recognition of ESCRT-III by the AAA ATPase Vps4. Nature 449, 735-744 https://doi.org/10.1038/nature06171
- Stuchell-Brereton, M. D., Skalicky, J. J., Kieffer, C., Karren, M. A., Ghaffarian, S. and Sundquist, W. I. (2007) ESCRT-III recognition by VPS4 ATPases. Nature 449, 740-744 https://doi.org/10.1038/nature06172
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