Apoptosis and cell death

Apolist: monthly literature updates for researchers

Archive for April, 2009

Apolist march 2009

Posted by cris on April 3, 2009

APOLIST – MARCH 2009
© Cristina Muñoz-Pinedo


TAK1 activates AMPK-dependent cytoprotective autophagy in TRAIL-treated epithelial cells
Griselda Herrero-Martín, Maria Høyer-Hansen, Celina García-García, Claudia Fumarola, Thomas Farkas, Abelardo López-Rivas and Marja Jäättelä
http://www.nature.com/emboj/journal/v28/n6/full/emboj20098a.html

Intrinsic Tumor Suppression and Epithelial Maintenance by Endocytic Activation of Eiger/TNF Signaling in Drosophila
T. Igaki, J.C. Pastor-Pareja, H. Aonuma, M. Miura, and T. Xu
http://www.cell.com/developmental-cell/abstract/S1534-5807%2809%2900030-6

BH3 / mitochondria


Dynamics of outer mitochondrial membrane permeabilization during apoptosis
M Rehm, H J Huber, C T Hellwig, S Anguissola, H Dussmann & J H M Prehn
http://www.nature.com/cdd/journal/v16/n4/full/cdd2008187a.html

Bcl-xL increases mitochondrial fission, fusion, and biomass in neurons
Sarah B. Berman, Ying-bei Chen, Bing Qi, J. Michael McCaffery, Edmund B. Rucker, III, Sandra Goebbels, Klaus-Armin Nave, Beth A. Arnold, Elizabeth A. Jonas, Fernando J. Pineda, and J. Marie Hardwick
http://jcb.rupress.org/cgi/content/abstract/184/5/707?etoc

Puma indirectly activates Bax to cause apoptosis in the absence of Bid or Bim
A M Jabbour, J E Heraud, C P Daunt, T Kaufmann, J Sandow, L A O’Reilly, B A Callus, A Lopez, A Strasser, D L Vaux & P G Ekert
http://www.nature.com/cdd/journal/v16/n4/full/cdd2008179a.html

Role of BNIP3 in TNF-induced cell death — TNF upregulates BNIP3 expression
Saeid Ghavami, Mehdi Eshraghi, Kamran Kadkhoda, Mark M. Mutawe, Subbareddy Maddika, Graham H. Bay, Sebastian Wesselborg, Andrew J. Halayko, Thomas Klonisch, Marek Los
http://dx.doi.org/10.1016/j.bbamcr.2009.01.002

Mitogen-Activated Protein Kinase Inhibition Induces Translocation of Bmf to Promote Apoptosis in Melanoma
Matthew W. VanBrocklin, Monique Verhaegen, Maria S. Soengas, and Sheri L. Holmen
Cancer Res 2009;69 1985-1994
http://cancerres.aacrjournals.org/cgi/content/abstract/69/5/1985

Mechanism of Bcl-2 and Bcl-XL inhibition of NLRP1 inflammasome: Loop domain-dependent suppression of ATP binding and oligomerization
Benjamin Faustin, Ya Chen, Dayong Zhai, Gaelle Le Negrate, Lydia Lartigue, Arnold Satterthwait, and John C. Reed
http://www.pnas.org/content/106/10/3935.abstract?etoc

Molecular basis for BH3 domain recognition in the BCL-2 protein family:Identification of conserved hot-spot interactions
Gautier Moroy, Elyette Martin, Annick Dejaegere, and Roland H. Stote
http://www.jbc.org/cgi/content/abstract/M805542200v1

Selective roles for antiapoptotic MCL-1 during granulocyte development and macrophage effector function
Desiree A. Steimer, Kelli Boyd, Osamu Takeuchi, Jill K. Fisher, Gerard P. Zambetti, and Joseph T. Opferman
Blood 2009;113 2805-2815
http://bloodjournal.hematologylibrary.org/cgi/content/abstract/113/12/2805

MYC-induced myeloid leukemogenesis is accelerated by all six members of the antiapoptotic BCL family
L J Beverly & H E Varmus
http://www.nature.com/onc/journal/v28/n9/full/onc2008466a.html

P53 acetylation is crucial for its transcription-independent proapoptotic functions
Hirohito Yamaguchi, Nicholas T. Woods, Landon G. Piluso, Heng-Huan Lee, Jiandong Chen, Kapil N. Bhalla, Alvaro Monteiro, Xuan Liu, Mien-Chie Hung, and Hong-Gang Wang
http://www.jbc.org/cgi/content/abstract/M809268200v1

BH3-only protein Bim more critical than Puma in tyrosine kinase inhibitor–induced apoptosis of human leukemic cells and transduced hematopoietic progenitors carrying oncogenic FLT3
Amanda Nordigården, Maria Kraft, Pernilla Eliasson, Verena Labi, Eric W.-F. Lam, Andreas Villunger, and Jan-Ingvar Jönsson
http://bloodjournal.hematologylibrary.org/cgi/content/abstract/113/10/2302

BCL-2 expression and p38MAPK activity in cells infected with influenza a virus: Impact on virally induced apoptosis and viral replication
Lucia Nencioni, Giovanna De Chiara, Rossella Sgarbanti, Donatella Amatore, Katia Aquilano, Maria E. Marcocci, Annalucia Serafino, Maria Torcia, Federico Cozzolino, Maria R. Ciriolo, Enrico Garaci, and Anna T. Palamara
http://www.jbc.org/cgi/content/abstract/M900146200v1

Assembly of the mitochondrial apoptosis-induced channel, MAC
Sonia Martinez-Caballero, Laurent M. Dejean, Michael S. Kinnally, Kyoung Joon Oh, Carmen A. Mannella, and Kathleen W. Kinnally
http://www.jbc.org/cgi/content/abstract/M806610200v1

CICD


Modulation of Caspase-Independent Cell Death Leads to Resensitization of Imatinib Mesylate–Resistant Cells
Vanessa J. Lavallard, Ludivine A. Pradelli, Audrey Paul, Marie Bénéteau, Arnaud Jacquel, Patrick Auberger, and Jean-Ehrland Ricci
Cancer Res 2009;69 3013-3020
http://cancerres.aacrjournals.org/cgi/content/abstract/69/7/3013

Copper-dopamine complex induces mitochondrial autophagy preceding caspase-independent apoptotic cell death
Irmgard Paris, Carolina Perez-Pastene, Eduardo Couve, Pablo Caviedes, Susan LeDoux, and Juan Segura-Aguilar
http://www.jbc.org/cgi/content/abstract/M900323200v1

Death receptors


HIV Induces TRAIL Sensitivity in Hepatocytes
Challagundla K. Babu1, Kanitta Suwansrinon1, Gary D. Bren1, Andrew D. Badley1,2, Stacey A. Rizza
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0004623

Oxaliplatin enhances TRAIL-induced apoptosis in gastric cancer cells by CBL-regulated death receptor redistribution in lipid rafts
Pages 943-948
Ling Xu, Xiujuan Qu, Ye Zhang, Xuejun Hu, Xianghong Yang, Kezuo Hou, Yuee Teng, Jingdong Zhang, Kiyonao Sada, Yunpeng Liu
http://dx.doi.org/10.1016/j.febslet.2009.02.014

IAPs


S-nitrosylation of XIAP compromises neuronal survival in Parkinson’s disease
Anthony H. K. Tsang, Yun-IL Lee, Han Seok Ko, Joseph M. Savitt, Olga Pletnikova, Juan C. Troncoso, Valina L. Dawson, Ted M. Dawson, and Kenny K. K. Chung
http://www.pnas.org/content/106/12/4900.abstract?etoc

Small Molecule XIAP Inhibitors Enhance TRAIL-Induced Apoptosis and Antitumor Activity in Preclinical Models of Pancreatic Carcinoma
Meike Vogler, Henning Walczak, Dominic Stadel, Tobias L. Haas, Felicitas Genze, Marjana Jovanovic, Umesh Bhanot, Cornelia Hasel, Peter Möller, Jürgen E. Gschwend, Thomas Simmet, Klaus-Michael Debatin, and Simone Fulda
Cancer Res 2009;69 2425-2434
http://cancerres.aacrjournals.org/cgi/content/abstract/69/6/2425

The E3 ubiquitin ligase cIAP1 binds and ubiquitinates caspases-3 and -7 via unique mechanisms at distinct steps in their processing
Young Eun Choi, Michael Butterworth, Srinivas Malladi, Colin S. Duckett, Gerald M. Cohen, and Shawn B. Bratton
J. Biol. Chem. published 3 March 2009, 10.1074/jbc.M807550200
http://www.jbc.org/cgi/content/abstract/M807550200v1

cIAP1, cIAP2, and XIAP Act Cooperatively via Nonredundant Pathways to Regulate Genotoxic Stress–Induced Nuclear Factor- B Activation
Hyung-Seung Jin, Dong-Hee Lee, Dong-Hwan Kim, Ji-Hye Chung, Seul-Ji Lee, and Tae H. Lee
Cancer Res 2009;69 1782-1791
http://cancerres.aacrjournals.org/cgi/content/abstract/69/5/1782

Caspases


Dynamic expression of epidermal caspase 8 simulates a wound healing response
Pedro Lee1, Dai-Jen Lee1, Carol Chan1, Shih-Wei Chen1, Irene Ch’en2 & Colin Jamora
http://www.nature.com/nature/journal/v458/n7237/full/nature07687.html

Self-activation of Caspase-6 in vitro and in vivo: Caspase-6 activation does not induce cell death in HEK293T cells
Pages 592-601
Guy Klaiman, Nathalie Champagne, Andréa C. LeBlanc
http://dx.doi.org/10.1016/j.bbamcr.2008.12.004

Caspase-7 deficiency protects from endotoxin-induced lymphocyte apoptosis and improves survival
Mohamed Lamkanfi, Lilian O. Moreira, Patrudu Makena, Diana C. J. Spierings, Kelli Boyd, Peter J. Murray, Douglas R. Green, and Thirumala-Devi Kanneganti
Blood 2009;113 2742-2745
http://bloodjournal.hematologylibrary.org/cgi/content/abstract/113/12/2742

A Breast Cancer Risk Haplotype in the Caspase-8 Gene
Neil Duncan Shephard, Ryan Abo, Sushila Harkisandas Rigas, Bernd Frank, Wei-Yu Lin, Ian Wallace Brock, Adam Shippen, Sabapathy Prakash Balasubramanian, Malcolm Walter Ronald Reed, Claus Rainer Bartram, Alfons Meindl, Rita Katharina Schmutzler, Christoph Engel, Barbara Burwinkel, Lisa Anne Cannon-Albright, Kristina Allen-Brady, Nicola Jane Camp, and Angela Cox
Cancer Res 2009;69 2724-2728
http://cancerres.aacrjournals.org/cgi/content/abstract/69/7/2724

Immunity


Visualizing CTL activity for different CD8+ effector T cells supports the idea that lower TCR/epitope avidity may be advantageous for target cell killing
M R Jenkins, N L La Gruta, P C Doherty, J A Trapani, S J Turner & N J Waterhouse
http://www.nature.com/cdd/journal/v16/n4/full/cdd2008176a.html

Innate immune recognition of infected apoptotic cells directs TH17 cell differentiation
Miriam Beer Torchinsky, Johan Garaude, Andrea P. Martin and J. Magarian Blander
http://www.nature.com/nature/journal/v458/n7234/full/nature07781.html

Mechanisms of pre-apoptotic calreticulin exposure in immunogenic cell death
Theocharis Panaretakis, Oliver Kepp, Ulf Brockmeier, Antoine Tesniere, Ann-Charlotte Bjorklund, Daniel C Chapman, Michael Durchschlag, Nicholas Joza, Gérard Pierron, Peter van Endert, Junying Yuan, Laurence Zitvogel, Frank Madeo, David B Williams and Guido Kroemer
http://www.nature.com/emboj/journal/v28/n5/abs/emboj20091a.html

Other


BAX Inhibitor-1 Is a Negative Regulator of the ER Stress Sensor IRE1α
F. Lisbona, D. Rojas-Rivera, P. Thielen, S. Zamorano, D. Todd, F. Martinon, A. Glavic, C. Kress, J.H. Lin, P. Walter, J.C. Reed, L.H. Glimcher, and C. Hetz
http://www.cell.com/molecular-cell/abstract/S1097-2765%2809%2900133-6

Human initiator caspases trigger apoptotic and autophagic phenotypes in Saccharomyces cerevisiae
Pages 561-571
Patricia Lisa-Santamaría, Aaron M. Neiman, Álvaro Cuesta-Marbán, Faustino Mollinedo, José L. Revuelta, Alberto Jiménez
http://dx.doi.org/10.1016/j.bbamcr.2008.12.016

Vacuolar functions determine the mode of cell death
[in yeast]
Alexandra Schauer, Heide Knauer, Christoph Ruckenstuhl, Heike Fussi, Michael Durchschlag, Ulrike Potocnik, Kai-Uwe Fröhlich
http://dx.doi.org/10.1016/j.bbamcr.2008.11.006

REVIEWS / COMMENTS


Many reviews on cell death and disease in Apoptosis (the journal)
http://www.springerlink.com/content/x0k422557704/?p=9f68203c1a2445c6b90444d85acbb875&pi=0

Ubiquitin-mediated regulation of apoptosis
Meike Broemer, Pascal Meier
http://dx.doi.org/10.1016/j.tcb.2009.01.004

Immunology: Cause of death matters
Brigitta Stockinger
http://www.nature.com/nature/journal/v458/n7234/full/458044a.html

Lysosomal involvement in cell death and cancer
Thomas Kirkegaard, Marja Jäättelä
http://dx.doi.org/10.1016/j.bbamcr.2008.09.008

A caspase homolog keeps CED-3 in check
Graham F. Brady, Colin S. Duckett
http://dx.doi.org/10.1016/j.tibs.2008.11.003

Intricate Links between ER Stress and Apoptosis
F. Madeo and G. Kroemer
http://dx.doi.org/10.1016/j.molcel.2009.03.002

The role of Bcl-2 family member BNIP3 in cell death and disease: NIPping at the heels of cell death
T R Burton & S B Gibson
http://www.nature.com/cdd/journal/v16/n4/full/cdd2008185a.html

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