A novel calcium-binding protein is associated with tau proteins in tauopathy

被引:57
作者
Vega, Irving E. [1 ,2 ]
Traverso, Edwin E. [1 ]
Ferrer-Acosta, Yancy [1 ]
Matos, Eduardo [1 ]
Colon, Migdalisel [1 ]
Gonzalez, John [3 ]
Dickson, Dennis [3 ]
Hutton, Michael [3 ]
Lewis, Jade [3 ]
Yen, Shu H. [3 ]
机构
[1] Univ Puerto Rico, Dept Biol, San Juan, PR 00931 USA
[2] Univ Puerto Rico, Dept Biol, Prot Mass Spectrometry, San Juan, PR 00936 USA
[3] Mayo Clin Jacksonville, Mayo Clin Coll Med, Dept Neurosci, Jacksonville, FL 32224 USA
关键词
Alzheimer's disease; calcium; EF-hand domain; tau; tauopathy;
D O I
10.1111/j.1471-4159.2008.05339.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Tauopathies are a group of neurological disorders characterized by the presence of intraneuronal hyperphosphorylated and filamentous tau. Mutations in the tau gene have been found in kindred with tauopathy. The expression of the human tau mutant in transgenic mice induced neurodegeneration, indicating that tau plays a central pathological role. However, the molecular mechanism leading to tau-mediated neurodegeneration is poorly understood. To gain insights into the role that tau plays in neurodegeneration, human tau proteins were immunoprecipitated from brain lysates of the tauopathy mouse model JNPL3, which develops neurodegeneration in age-dependent manner. In the present work, a novel EF-hand domain-containing protein was found associated with tau proteins in brain lysate of 12-month-old JNPL3 mice. The association between tau proteins and the novel identified protein appears to be induced by the neurodegeneration process as these two proteins were not found associated in young JNPL3 mice. Consistently, the novel protein co-purified with the pathological sarkosyl insoluble tau in terminally ill JNPL3 mice. Calcium-binding assays demonstrated that this protein binds calcium effectively. Finally, the association between tau and the novel calcium-binding protein is conserved in human and enriched in Alzheimer's disease brain. Taken together, the identification of a novel calcium-binding protein associated with tau protein in terminally ill tauopathy mouse model and its confirmation in human brain lysate suggests that this association may play an important physiological and/or pathological role.
引用
收藏
页码:96 / 106
页数:11
相关论文
共 31 条
[1]
Hyperphosphorylated tan and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5 [J].
Ahlijanian, MK ;
Barrezueta, NX ;
Williams, RD ;
Jakowski, A ;
Kowsz, KP ;
McCarthy, S ;
Coskran, T ;
Carlo, A ;
Seymour, PA ;
Burkhardt, JE ;
Nelson, RB ;
McNeish, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2910-2915
[2]
The novel adaptor protein Swiprosin-1 enhances BCR signals and contributes to BCR-induced apoptosis [J].
Avramidou, A. ;
Kroczek, C. ;
Lang, C. ;
Schuh, W. ;
Jaeck, H-M ;
Mielenz, D. .
CELL DEATH AND DIFFERENTIATION, 2007, 14 (11) :1936-1947
[3]
Tau-mediated neurodegeneration in Alzheimer's disease and related disorders [J].
Ballatore, Carlo ;
Lee, Virginia M. -Y. ;
Trojanowski, John Q. .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (09) :663-672
[4]
Accumulation of pathological tau species and memory loss in a conditional model of tauopathy [J].
Berger, Zdenek ;
Roder, Hanno ;
Hanna, Amanda ;
Carlson, Aaron ;
Rangachari, Vijayaraghavan ;
Yue, Mei ;
Wszolek, Zbigniew ;
Ashe, Karen ;
Knight, Joshua ;
Dickson, Dennis ;
Andorfer, Cathy ;
Rosenberry, Terrone L. ;
Lewis, Jada ;
Hutton, Mike ;
Janus, Christopher .
JOURNAL OF NEUROSCIENCE, 2007, 27 (14) :3650-3662
[5]
Aberrant Cdk5 activation by p25 triggers pathological events leading to neurodegeneration and neurofibrillary tangles [J].
Cruz, JC ;
Tseng, HC ;
Goldman, JA ;
Shih, H ;
Tsai, LH .
NEURON, 2003, 40 (03) :471-483
[6]
The high-affinity HSP90-CHIP complex recognizes and selectively degrades phosphorylated tau client proteins [J].
Dickey, Chad A. ;
Kamal, Adeela ;
Lundgren, Karen ;
Klosak, Natalia ;
Bailey, Rachel M. ;
Dunmore, Judith ;
Ash, Peter ;
Shoraka, Sareh ;
Zlatkovic, Jelena ;
Eckman, Christopher B. ;
Patterson, Cam ;
Dickson, Dennis W. ;
Nahman, N. Stanley, Jr. ;
Hutton, Michael ;
Burrows, Francis ;
Petrucelli, Leonard .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (03) :648-658
[7]
HSP induction mediates selective clearance of tau phosphorylated at proline-directed Ser/Thr sites but not KXGS (MARK) sites [J].
Dickey, Chad A. ;
Dunmore, Judith ;
Lu, Bingwei ;
Wang, Ji-Wu ;
Lee, Wing C. ;
Kamal, Adeela ;
Burrows, Francis ;
Eckman, Christopher ;
Hutton, Michael ;
Petrucelli, Leonard .
FASEB JOURNAL, 2006, 20 (02) :753-+
[8]
Chaperones increase association of tau protein with microtubules [J].
Dou, F ;
Netzer, WJ ;
Tanemura, K ;
Li, F ;
Hartl, FU ;
Takashima, A ;
Gouras, GK ;
Greengard, P ;
Xu, HX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (02) :721-726
[9]
Abnormal bundling and accumulation of F-actin mediates tau-induced neuronal degeneration in vivo [J].
Fulga, Tudor A. ;
Elson-Schwab, Ilan ;
Khurana, Vikram ;
Steinhilb, Michelle L. ;
Spires, Tara L. ;
Hyman, Bradley T. ;
Feany, Mel B. .
NATURE CELL BIOLOGY, 2007, 9 (02) :139-U17
[10]
GLYCOGEN-SYNTHASE KINASE-3 INDUCES ALZHEIMERS DISEASE-LIKE PHOSPHORYLATION OF TAU - GENERATION OF PAIRED HELICAL FILAMENT EPITOPES AND NEURONAL LOCALIZATION OF THE KINASE [J].
HANGER, DP ;
HUGHES, K ;
WOODGETT, JR ;
BRION, JP ;
ANDERTON, BH .
NEUROSCIENCE LETTERS, 1992, 147 (01) :58-62