Tumor necrosis factor receptor 2 (TNFR2)•interleukin-17 receptor d (IL-17RD) heteromerization reveals a novel mechanism for NF-κB activation

Journal of Biological Chemistry

Volumn 290, Issue 2, 2015, Pages 861-871

  Yang, Shigao ^a,b,c   Wang, Yinyin ^a,b   Mei, Kunrong ^d   Zhang, Sen ^e   Sun, Xiaojun ^a,b   Ren, Fangli ^a,b   Liu, Sihan ^a,b   Yang, Zi ^a,b   Wang, Xinquan ^d   Qin, Zhihai ^f   Chang, Zhijie ^a,b  

^a Tsinghua University   (China)

^b SICHUAN UNIVERSITY   (China)

^c INSTITUTE OF PROCESS ENGINEERING   (China)

^d Tsinghua University   (China)

^e INSTITUTE OF MATERIA MEDICA   (China)

^f INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; BIOLOGY;

AUTOIMMUNE DISEASE; EPITHELIAL CELLS; INFLAMMATORY DISEASE; INTERLEUKIN-17; RENAL EPITHELIA; STRONG INTERACTION; TUMOR NECROSIS FACTOR RECEPTORS;

CHEMICAL ACTIVATION;

IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 17 RECEPTOR; INTERLEUKIN 17 RECEPTOR D; MESSENGER RNA; TUMOR NECROSIS FACTOR RECEPTOR 2; UNCLASSIFIED DRUG; TUMOR NECROSIS FACTOR RECEPTOR 1;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; FLUORESCENCE RESONANCE ENERGY TRANSFER; GENE EXPRESSION REGULATION; GENE OVEREXPRESSION; HETEROMERIZATION; IL 17RD GENE; IMMUNOREGULATION; IN VIVO STUDY; INTRACELLULAR SIGNALING; KIDNEY TUBULE CELL; MOUSE; NEPHRITIS; NONHUMAN; POLYMERIZATION; PROTEIN AGGREGATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; TRANSCRIPTION INITIATION; ANIMAL; CHEMISTRY; EPITHELIUM CELL; GENETICS; HUMAN; INFLAMMATION; KIDNEY DISTAL TUBULE; METABOLISM; PATHOLOGY; PROTEIN MULTIMERIZATION; RAT; SIGNAL TRANSDUCTION;

RATTUS;

ANIMALS; EPITHELIAL CELLS; HUMANS; INFLAMMATION; KIDNEY TUBULES, DISTAL; NEPHRITIS; NF-KAPPA B; PROTEIN MULTIMERIZATION; RATS; RECEPTORS, INTERLEUKIN-17; RECEPTORS, TUMOR NECROSIS FACTOR, TYPE I; RECEPTORS, TUMOR NECROSIS FACTOR, TYPE II; SIGNAL TRANSDUCTION; TRANSCRIPTIONAL ACTIVATION;

EID: 84920915339     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.586560     Document Type: Article

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