Targeting MALT1 Proteolytic Activity in Immunity, Inflammation and Disease: Good or Bad?

被引:64
作者
Demeyer, Annelies [1 ,2 ]
Staal, Jens [1 ,2 ]
Beyaert, Rudi [1 ,2 ]
机构
[1] Univ Ghent VIB, Inflammat Res Ctr, Unit Mol Signal Transduct Inflammat, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9052 Ghent, Belgium
关键词
NF-KAPPA-B; T-CELL; PARACASPASE MALT1; UBIQUITIN LIGASE; PHARMACOLOGICAL INHIBITION; COMBINED IMMUNODEFICIENCY; PROTEASE ACTIVITY; PROTECTS MICE; ACTIVATION; RECEPTOR;
D O I
10.1016/j.molmed.2015.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MALT1 is a signaling protein that plays a key role in immunity, inflammation, and lymphoid malignancies. For a long time MALT1 was believed to function as a scaffold protein, providing an assembly platform for other signaling proteins. This view changed dramatically when MALT1 was also found to have proteolytic activity and a capacity to fine-tune immune responses. Preclinical studies have fostered the belief that MALT1 is a promising therapeutic target in autoimmunity and B cell lymphomas. However, recent studies have shown that mice expressing catalytically-inactive MALT1 develop multi-organ inflammation and autoimmunity, and thus have tempered this initial enthusiasm. We discuss recent findings, highlighting the urgent need for a better mechanistic and functional understanding of MALT1 in host defense and disease.
引用
收藏
页码:135 / 150
页数:16
相关论文
共 100 条
[1]   MALT1-a universal soldier: multiple strategies to ensure NF-κB activation and target gene expression [J].
Afonina, Inna S. ;
Elton, Lynn ;
Carpentier, Isabelle ;
Beyaert, Rudi .
FEBS JOURNAL, 2015, 282 (17) :3286-3297
[2]   A novel gene, MALT1 at 18q21, is involved in t(11;18) (q21;q21) found in low-grade B-cell lymphoma of mucosa-associated lymphoid tissue [J].
Akagi, T ;
Motegi, M ;
Tamura, A ;
Suzuki, R ;
Hosokawa, Y ;
Suzuki, H ;
Ota, H ;
Nakamura, S ;
Morishima, Y ;
Taniwaki, M ;
Seto, M .
ONCOGENE, 1999, 18 (42) :5785-5794
[3]   Selective expansion of marginal zone B cells in Eμ-API2-MALT1 mice is linked to enhanced IκB kinase γ polyubiquitination [J].
Baens, Mathijs ;
Fevery, Sabine ;
Sagaert, Xavier ;
Noels, Heidi ;
Hagens, Sofie ;
Broeckx, Vicky ;
Billiau, An D. ;
De Wolf-Peeters, Christiane ;
Marynen, Peter .
CANCER RESEARCH, 2006, 66 (10) :5270-5277
[4]   MALT1 Auto-Proteolysis Is Essential for NF-κB-Dependent Gene Transcription in Activated Lymphocytes [J].
Baens, Mathijs ;
Bonsignore, Luca ;
Somers, Riet ;
Vanderheydt, Charlotte ;
Weeks, Stephen D. ;
Gunnarsson, Jenny ;
Nilsson, Ewa ;
Roth, Robert G. ;
Thome, Margot ;
Marynen, Peter .
PLOS ONE, 2014, 9 (08)
[5]   An E3 ubiquitin ligase-independent role of LUBAC [J].
Beyaert, Rudi .
BLOOD, 2014, 123 (14) :2131-2133
[6]   Deficiency of MALT1 Paracaspase Activity Results in Unbalanced Regulatory and Effector T and B Cell Responses Leading to Multiorgan Inflammation [J].
Bornancin, Frederic ;
Renner, Florian ;
Touil, Ratiba ;
Sic, Heiko ;
Kolb, Yeter ;
Touil-Allaoui, Ismahane ;
Rush, James S. ;
Smith, Paul A. ;
Bigaud, Marc ;
Junker-Walker, Ursula ;
Burkhart, Christoph ;
Dawson, Janet ;
Niwa, Satoru ;
Katopodis, Andreas ;
Nuesslein-Hildesheim, Barbara ;
Weckbecker, Gisbert ;
Zenke, Gerhard ;
Kinzel, Bernd ;
Traggiai, Elisabetta ;
Brenner, Dirk ;
Bruestle, Anne ;
Paul, Michael St. ;
Zamurovic, Natasa ;
Mccoy, Kathy D. ;
Rolink, Antonius ;
Regnier, Catherine H. ;
Mak, Tak W. ;
Ohashi, Pamela S. ;
Patel, Dhavalkumar D. ;
Calzascia, Thomas .
JOURNAL OF IMMUNOLOGY, 2015, 194 (08) :3723-3734
[7]   Platelet-Activating Factor-Induced NF-κB Activation and IL-8 Production in Intestinal Epithelial Cells Are Bcl10-Dependent [J].
Borthakur, Alip ;
Bhattacharyya, Sumit ;
Alrefai, Waddah A. ;
Tobacman, Joanne K. ;
Ramaswamy, Krishnamurthy ;
Dudeja, Pradeep K. .
INFLAMMATORY BOWEL DISEASES, 2010, 16 (04) :593-603
[8]   The NF-κB regulator MALT1 determines the encephalitogenic potential of Th17 cells [J].
Bruestle, Anne ;
Brenner, Dirk ;
Knobbe, Christiane B. ;
Lang, Philipp A. ;
Virtanen, Carl ;
Hershenfield, Brian M. ;
Reardon, Colin ;
Lacher, Sonja M. ;
Ruland, Juergen ;
Ohashi, Pamela S. ;
Mak, Tak W. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (12) :4698-4709
[9]  
Brustle A, 2015, CELL DEATH DIFFER
[10]  
Cain C, 2014, SCIBX, V7, P133, DOI DOI 10.1038/SCIBX.2014.133