The TRPC6 intronic polymorphism, associated with the risk of neurological disorders in systemic lupus erythematous, influences immune cell function

被引:11
作者
Ramirez, Giuseppe A. [1 ,3 ]
Coletto, Lavinia A. [3 ]
Bozzolo, Enrica P. [1 ]
Citterio, Lorena [4 ]
Carpini, Simona Delli [4 ]
Zagato, Laura [4 ]
Rovere-Querini, Patrizia [1 ,2 ,3 ]
Lanzani, Chiara [4 ]
Manunta, Paolo [4 ]
Manfredi, Angelo A. [1 ,2 ,3 ]
Sciorati, Clara [2 ]
机构
[1] IRCCS San Raffaele Hosp & Sci Inst, Unit Immunol Rheumatol Allergy & Rare Dis, Milan, Italy
[2] San Raffaele Hosp & Sci Inst, Div Immunol Transplantat & Infect Dis, Milan, Italy
[3] Univ Vita Salute San Raffaele, Milan, Italy
[4] IRCCS San Raffaele Hosp & Sci Inst, Unit Nephrol, Milan, Italy
关键词
TRPC6; Systemic lupus erythematous; Neuropsychiatric; Calcium; Apoptosis; Cytokines; Genetics; DISEASE-ACTIVITY INDEX; T-CELLS; TRANSCRIPTION FACTORS; GENETIC-VARIANTS; B-CELLS; CALCIUM; APOPTOSIS; COLLEGE; PATHWAY; CHANNEL;
D O I
10.1016/j.jneuroim.2018.10.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with systemic lupus erythematosus (SLE) carrying a TT genotype for the rs7925662 single nucleotide polymorphism (SNP) in the transient receptor potential canonical channel 6 (TRPC6) gene are more likely to develop neuropsychiatric manifestations (NPSLE). We functionally characterised the effects of TRPC6 on peripheral blood mononuclear cells from 18 patients with SLE and 8 healthy controls with a known genotype. TRPC6 influenced calcium currents, apoptosis rates and cytokine secretion in a disease- and genotype-dependent manner. Cells from TT patients with NPSLE were more dependent on TRPC6 for the generation of calcium currents.
引用
收藏
页码:43 / 53
页数:11
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