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Volumn 5, Issue 10, 2010, Pages

Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy

Author keywords

[No Author keywords available]

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; MESSENGER RNA; PROGRANULIN; TAR DNA BINDING PROTEIN; DNA BINDING PROTEIN; GRN PROTEIN, HUMAN; PROTEIN TDP-43; SIGNAL PEPTIDE; SUPEROXIDE DISMUTASE;

EID: 78149429744     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0013368     Document Type: Article
Times cited : (121)

References (33)
  • 1
    • 70349687630 scopus 로고    scopus 로고
    • Roles of progranulin in sexual differentiation of the developing brain and adult neurogenesis
    • Suzuki M, Lee HC, Kayasuga Y, Chiba S, Nedachi T, et al. (2009) Roles of progranulin in sexual differentiation of the developing brain and adult neurogenesis. J Reprod Dev 55: 351-355.
    • (2009) J Reprod Dev , vol.55 , pp. 351-355
    • Suzuki, M.1    Lee, H.C.2    Kayasuga, Y.3    Chiba, S.4    Nedachi, T.5
  • 2
    • 0031854765 scopus 로고    scopus 로고
    • Granulins: The structure and function of an emerging family of growth factors
    • Bateman A, Bennett HP (1998) Granulins: the structure and function of an emerging family of growth factors. J Endocrinol 158: 145-151.
    • (1998) J Endocrinol , vol.158 , pp. 145-151
    • Bateman, A.1    Bennett, H.P.2
  • 3
    • 0242320195 scopus 로고    scopus 로고
    • Progranulin (granulin-epithelin precursor, PC-cellderived growth factor, acrogranin) mediates tissue repair and tumorigenesis
    • He Z, Bateman A (2003) Progranulin (granulin-epithelin precursor, PC-cellderived growth factor, acrogranin) mediates tissue repair and tumorigenesis. J Mol Med 81: 600-612.
    • (2003) J Mol Med , vol.81 , pp. 600-612
    • He, Z.1    Bateman, A.2
  • 4
    • 33847654643 scopus 로고    scopus 로고
    • Progranulin in front o tempora l l obar degener a t ion and neuroinf l ammati on
    • Ahmed Z, Mackenzie IR, Hutton ML, Dickson DW (2007) Progranulin in front o tempora l l obar degener a t ion and neuroinf l ammati on. J Neuroinflammation 4: 7.
    • (2007) J Neuroinflammation , vol.4 , pp. 7
    • Ahmed, Z.1    McKenzie, I.R.2    Hutton, M.L.3    Dickson, D.W.4
  • 5
    • 42049087853 scopus 로고    scopus 로고
    • Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
    • Van Damme P, Van Hoecke A, Lambrechts D, Vanacker P, Bogaert E, et al. (2008) Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival. J Cell Biol 181: 37-41.
    • (2008) J Cell Biol , vol.181 , pp. 37-41
    • Van Damme, P.1    Van Hoecke, A.2    Lambrechts, D.3    Vanacker, P.4    Bogaert, E.5
  • 6
    • 33746919083 scopus 로고    scopus 로고
    • Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    • Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, et al. (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442: 916-919.
    • (2006) Nature , vol.442 , pp. 916-919
    • Baker, M.1    McKenzie, I.R.2    Pickering-Brown, S.M.3    Gass, J.4    Rademakers, R.5
  • 7
    • 33746910649 scopus 로고    scopus 로고
    • Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    • Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, et al. (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442: 920-924.
    • (2006) Nature , vol.442 , pp. 920-924
    • Cruts, M.1    Gijselinck, I.2    van der Zee, J.3    Engelborghs, S.4    Wils, H.5
  • 8
    • 60949099072 scopus 로고    scopus 로고
    • Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide
    • Benussi L, Ghidoni R, Pegoiani E, Moretti DV, Zanetti O, et al. (2009) Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide. Neurobiol Dis 33: 379-385.
    • (2009) Neurobiol Dis , vol.33 , pp. 379-385
    • Benussi, L.1    Ghidoni, R.2    Pegoiani, E.3    Moretti, D.V.4    Zanetti, O.5
  • 9
    • 67249111266 scopus 로고    scopus 로고
    • Serum biomarker for progranulin-associated frontotemporal lobar degeneration
    • Sleegers K, Brouwers N, Van Damme P, Engelborghs S, Gijselinck I, et al. (2009) Serum biomarker for progranulin-associated frontotemporal lobar degeneration. Ann Neurol 65: 603-609.
    • (2009) Ann Neurol , vol.65 , pp. 603-609
    • Sleegers, K.1    Brouwers, N.2    Van Damme, P.3    Engelborghs, S.4    Gijselinck, I.5
  • 10
    • 64849103956 scopus 로고    scopus 로고
    • Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
    • Finch N, Baker M, Crook R, Swanson K, Kuntz K, et al. (2009) Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain 132: 583-591.
    • (2009) Brain , vol.132 , pp. 583-591
    • Finch, N.1    Baker, M.2    Crook, R.3    Swanson, K.4    Kuntz, K.5
  • 11
    • 33749632259 scopus 로고    scopus 로고
    • Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
    • Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, et al. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314: 130-133.
    • (2006) Science , vol.314 , pp. 130-133
    • Neumann, M.1    Sampathu, D.M.2    Kwong, L.K.3    Truax, A.C.4    Micsenyi, M.C.5
  • 12
    • 33750716074 scopus 로고    scopus 로고
    • TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
    • Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, et al. (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.
    • (2006) Biochem Biophys Res Commun , vol.351 , pp. 602-611
    • Arai, T.1    Hasegawa, M.2    Akiyama, H.3    Ikeda, K.4    Nonaka, T.5
  • 13
    • 34547663747 scopus 로고    scopus 로고
    • TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions
    • Cairns NJ, Neumann M, Bigio EH, Holm IE, Troost D, et al. (2007) TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol 171: 227-240.
    • (2007) Am J Pathol , vol.171 , pp. 227-240
    • Cairns, N.J.1    Neumann, M.2    Bigio, E.H.3    Holm, I.E.4    Troost, D.5
  • 15
    • 42649120983 scopus 로고    scopus 로고
    • TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
    • Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, et al. (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40: 572-574.
    • (2008) Nat Genet , vol.40 , pp. 572-574
    • Kabashi, E.1    Valdmanis, P.N.2    Dion, P.3    Spiegelman, D.4    McConkey, B.J.5
  • 17
    • 52949094629 scopus 로고    scopus 로고
    • Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
    • Rutherford NJ, Zhang YJ, Baker M, Gass JM, Finch NA, et al. (2008) Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. PLoS Genet 4: e1000193.
    • (2008) PLoS Genet , vol.4
    • Rutherford, N.J.1    Zhang, Y.J.2    Baker, M.3    Gass, J.M.4    Finch, N.A.5
  • 18
    • 41149180753 scopus 로고    scopus 로고
    • TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
    • Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, et al. (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319: 1668-1672.
    • (2008) Science , vol.319 , pp. 1668-1672
    • Sreedharan, J.1    Blair, I.P.2    Tripathi, V.B.3    Hu, X.4    Vance, C.5
  • 19
    • 41949100148 scopus 로고    scopus 로고
    • TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: A genetic and histopathological analysis
    • Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, et al. (2008) TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol 7: 409-416.
    • (2008) Lancet Neurol , vol.7 , pp. 409-416
    • Van Deerlin, V.M.1    Leverenz, J.B.2    Bekris, L.M.3    Bird, T.D.4    Yuan, W.5
  • 20
    • 3142628291 scopus 로고    scopus 로고
    • Word retrieval in amyotrophic lateral sclerosis: A functional magnetic resonance imaging study
    • Abrahams S, Goldstein LH, Simmons A, Brammer M, Williams SC, et al. (2004) Word retrieval in amyotrophic lateral sclerosis: a functional magnetic resonance imaging study. Brain 127: 1507-1517.
    • (2004) Brain , vol.127 , pp. 1507-1517
    • Abrahams, S.1    Goldstein, L.H.2    Simmons, A.3    Brammer, M.4    Williams, S.C.5
  • 21
    • 2642559477 scopus 로고    scopus 로고
    • Characterization of amyotrophic lateral sclerosis and frontotemporal dementia
    • Lomen-Hoerth C (2004) Characterization of amyotrophic lateral sclerosis and frontotemporal dementia. Dement Geriatr Cogn Disord 17: 337-341.
    • (2004) Dement Geriatr Cogn Disord , vol.17 , pp. 337-341
    • Lomen-Hoerth, C.1
  • 22
    • 23844441835 scopus 로고    scopus 로고
    • Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum
    • Mackenzie IR, Feldman HH (2005) Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum. J Neuropathol Exp Neurol 64: 730-739.
    • (2005) J Neuropathol Exp Neurol , vol.64 , pp. 730-739
    • McKenzie, I.R.1    Feldman, H.H.2
  • 23
    • 34249946466 scopus 로고    scopus 로고
    • Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
    • Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, et al. (2007) Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol 61: 427-434.
    • (2007) Ann Neurol , vol.61 , pp. 427-434
    • McKenzie, I.R.1    Bigio, E.H.2    Ince, P.G.3    Geser, F.4    Neumann, M.5
  • 24
    • 34247606414 scopus 로고    scopus 로고
    • TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation
    • Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, et al. (2007) TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation. Acta Neuropathol 113: 535-542.
    • (2007) Acta Neuropathol , vol.113 , pp. 535-542
    • Tan, C.F.1    Eguchi, H.2    Tagawa, A.3    Onodera, O.4    Iwasaki, T.5
  • 25
    • 34548740744 scopus 로고    scopus 로고
    • Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish
    • Lemmens R, Van Hoecke A, Hersmus N, Geelen V, D'Hollander I, et al. (2007) Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish. Hum Mol Genet 16: 2359-2365.
    • (2007) Hum Mol Genet , vol.16 , pp. 2359-2365
    • Lemmens, R.1    Van Hoecke, A.2    Hersmus, N.3    Geelen, V.4    D'Hollander, I.5
  • 26
    • 77950360176 scopus 로고    scopus 로고
    • Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
    • Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, et al. (2010) Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo. Hum Mol Genet 19: 671-683.
    • (2010) Hum Mol Genet , vol.19 , pp. 671-683
    • Kabashi, E.1    Lin, L.2    Tradewell, M.L.3    Dion, P.A.4    Bercier, V.5
  • 27
    • 77649269011 scopus 로고    scopus 로고
    • TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
    • Wils H, Kleinberger G, Janssens J, Pereson S, Joris G, et al. (2010) TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci U S A 107: 3858-3863.
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 3858-3863
    • Wils, H.1    Kleinberger, G.2    Janssens, J.3    Pereson, S.4    Joris, G.5
  • 28
    • 70349246333 scopus 로고    scopus 로고
    • Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis
    • Luquin N, Yu B, Saunderson RB, Trent RJ, Pamphlett R (2009) Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis. Neuromuscul Disord 19: 696-700.
    • (2009) Neuromuscul Disord , vol.19 , pp. 696-700
    • Luquin, N.1    Yu, B.2    Saunderson, R.B.3    Trent, R.J.4    Pamphlett, R.5
  • 29
    • 70449521091 scopus 로고    scopus 로고
    • Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
    • Neumann M, Roeber S, Kretzschmar HA, Rademakers R, Baker M, et al. (2009) Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease. Acta Neuropathol 118: 605-616.
    • (2009) Acta Neuropathol , vol.118 , pp. 605-616
    • Neumann, M.1    Roeber, S.2    Kretzschmar, H.A.3    Rademakers, R.4    Baker, M.5
  • 31
    • 73249152831 scopus 로고    scopus 로고
    • TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
    • Wegorzewska I, Bell S, Cairns NJ, Miller TM, Baloh RH (2009) TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci U S A 106: 18809-18814.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 18809-18814
    • Wegorzewska, I.1    Bell, S.2    Cairns, N.J.3    Miller, T.M.4    Baloh, R.H.5
  • 32
    • 38349173569 scopus 로고    scopus 로고
    • Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion
    • Shankaran SS, Capell A, Hruscha AT, Fellerer K, Neumann M, et al. (2008) Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. J Biol Chem 283: 1744-1753.
    • (2008) J Biol Chem , vol.283 , pp. 1744-1753
    • Shankaran, S.S.1    Capell, A.2    Hruscha, A.T.3    Fellerer, K.4    Neumann, M.5
  • 33
    • 33746312670 scopus 로고    scopus 로고
    • Role of heat shock response and Hsp27 in mutant SOD1-dependent cell death
    • Krishnan J, Lemmens R, Robberecht W, Van Den Bosch L (2006) Role of heat shock response and Hsp27 in mutant SOD1-dependent cell death. Exp Neurol 200: 301-310.
    • (2006) Exp Neurol , vol.200 , pp. 301-310
    • Krishnan, J.1    Lemmens, R.2    Robberecht, W.3    Van Den Bosch, L.4


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