Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (33)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Götz, R.
Right arrow Articles by Sendtner, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Götz, R.
Right arrow Articles by Sendtner, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2000, Vol. 9, No. 17 2479-2489
© 2000 Oxford University Press

The neuronal apoptosis inhibitory protein suppresses neuronal differentiation and apoptosis in PC12 cells

Rudolf Götz+, Christoph Karch, Matthew R. Digby, Jakob Troppmair1, Ulf R. Rapp1 and Michael Sendtner

Klinische Forschergruppe Neuroregeneration, Department of Neurology a/nd 1Institute für Medizinische Strahlenkunde und Zellforschung, University of Würzburg, Versbacher Strasse 5, D-97080 Würzburg, Germany

The human neuronal apoptosis inhibitory protein (NAIP) gene has been discovered as a candidate gene for spinal muscular atrophy, a genetic disorder characterized by motor neuron loss in the spinal cord. The telomeric NAIP gene on human chromosome 5 is deleted together with survival motor neurons (SMN) in many cases of the most severe forms of the disorder. NAIP, c-IAP1 (inhibitor of apoptosis-1), c-IAP2, X-IAP, survivin and Apollon comprise the mammalian inhibitors of the apoptosis family and contain an N-terminal domain with 1–3 imperfect repeats of an ~65 amino acids domain named the baculovirus IAP repeat (BIR) motif. We identified six NAIP genes in the mouse genome which were found to be expressed in a broad range of tissues. Furthermore, we have investigated the effects of NAIP in the rat pheochromocytoma PC12 cell line. These cells differentiate in the presence of nerve growth factor (NGF) into cells that resemble sympathetic neurons. We observed that NAIP overexpression impaired NGF-induced neurite outgrowth. The BIR motifs of NAIP (residues 1345) were not required for this effect. However, the BIR domains of NAIP were essential to prevent apoptosis in PC12 cells after NGF deprivation or TNF-{alpha} receptor stimulation. Expression of full-length but not BIR-deleted-NAIP protects against cell death. This correlates with reduced activity of the cell death effector protease, caspase-3, in lysates of NAIP-PC12 cells, as measured by cleavage of the fluorogenic tetrapeptide substrate Asp-Glu-Val-Asp. Thus, unregulation of cellular differentiation and/or caspase suppression may contribute to motoneuron dysfunction and cell death in spinal muscular atrophy where NAIP is mutated.

+ To whom correspondence should be addressed. Tel: +49 931 201 3849; Fax: +49 931 201 3835; Email: goetz@mail.uni-wuerzburg.de


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
haematolHome page
B. I. Ferreira, J. F. Garcia, J. Suela, M. Mollejo, F. I. Camacho, A. Carro, S. Montes, M. A. Piris, and J. C. Cigudosa
Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasia
Haematologica, May 1, 2008; 93(5): 670 - 679.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
J. K.X. Maier, S. Balabanian, C. R. Coffill, A. Stewart, L. Pelletier, D. J. Franks, N. H. Gendron, and A. E. MacKenzie
Distribution of Neuronal Apoptosis Inhibitory Protein in Human Tissues
J. Histochem. Cytochem., September 1, 2007; 55(9): 911 - 923.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
P. Fernando and L. A. Megeney
Is caspase-dependent apoptosis only cell differentiation taken to the extreme?
FASEB J, January 1, 2007; 21(1): 8 - 17.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
A. Dziarmaga, P.-A. Hueber, D. Iglesias, N. Hache, A. Jeffs, N. Gendron, A. MacKenzie, M. Eccles, and P. Goodyer
Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2
Am J Physiol Renal Physiol, October 1, 2006; 291(4): F913 - F920.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
D. F. Moore, H. Li, N. Jeffries, V. Wright, R. A. Cooper Jr, A. Elkahloun, M. P. Gelderman, E. Zudaire, G. Blevins, H. Yu, et al.
Using Peripheral Blood Mononuclear Cells to Determine a Gene Expression Profile of Acute Ischemic Stroke: A Pilot Investigation
Circulation, January 18, 2005; 111(2): 212 - 221.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
S. Plenchette, S. Cathelin, C. Rebe, S. Launay, S. Ladoire, O. Sordet, T. Ponnelle, N. Debili, T.-H. Phan, R.-A. Padua, et al.
Translocation of the inhibitor of apoptosis protein c-IAP1 from the nucleus to the Golgi in hematopoietic cells undergoing differentiation: a nuclear export signal-mediated event
Blood, October 1, 2004; 104(7): 2035 - 2043.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
M. Harada, K.-i. Seino, H. Wakao, S. Sakata, Y. Ishizuka, T. Ito, S. Kojo, T. Nakayama, and M. Taniguchi
Down-regulation of the invariant V{alpha}14 antigen receptor in NKT cells upon activation
Int. Immunol., February 1, 2004; 16(2): 241 - 247.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. G. Sanna, J. d. S. Correia, O. Ducrey, J. Lee, K. Nomoto, N. Schrantz, Q. L. Deveraux, and R. J. Ulevitch
IAP Suppression of Apoptosis Involves Distinct Mechanisms: the TAK1/JNK1 Signaling Cascade and Caspase Inhibition
Mol. Cell. Biol., March 15, 2002; 22(6): 1754 - 1766.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
B. W. M. Jordan, D. Dinev, V. LeMellay, J. Troppmair, R. Gotz, L. Wixler, M. Sendtner, S. Ludwig, and U. R. Rapp
Neurotrophin Receptor-interacting Mage Homologue Is an Inducible Inhibitor of Apoptosis Protein-interacting Protein That Augments Cell Death
J. Biol. Chem., October 19, 2001; 276(43): 39985 - 39989.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
U. Schweizer, J. Gunnersen, C. Karch, S. Wiese, B. Holtmann, K. Takeda, S. Akira, and M. Sendtner
Conditional gene ablation of Stat3 reveals differential signaling requirements for survival of motoneurons during development and after nerve injury in the adult
J. Cell Biol., January 21, 2002; 156(2): 287 - 298.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.