نتایج جستجو برای: btk expression

تعداد نتایج: 873168  

Journal: :The Journal of biological chemistry 2001
K Saito A M Scharenberg J P Kinet

Bruton's tyrosine kinase (Btk) binds to phosphatidylinositol-3,4,5-trisphosphate (PtdIns-3,4,5-P(3)) through the Btk pleckstrin homology (PH) domain, an interaction thought to be required for Btk membrane translocation during B cell receptor signaling. Here, we report that interaction of PtdIns-3,4,5-P(3) with the PH domain of Btk directly induces Btk enzymatic activation in an in vitro kinase ...

2018
Samantha A Chalmers Jing Wen Jessica Doerner Ariel Stock Carla M Cuda Hadijat M Makinde Harris Perlman Todd Bosanac Deborah Webb Gerald Nabozny Jay S Fine Elliott Klein Meera Ramanujam Chaim Putterman

BACKGROUND Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that affects different end organs, including skin and brain. We and others have previously shown the importance of macrophages in the pathogenesis of cutaneous and neuropsychiatric lupus. Additionally, autoantibodies produced by autoreactive B cells are thought to play a role in both the skin and central nervous syst...

Journal: :Journal of immunology 2005
Miguel E Moreno-García Lucia N López-Bojórques Alejandro Zentella Lisa A Humphries David J Rawlings Leopoldo Santos-Argumedo

The CD38 cell surface receptor is a potent activator for splenic, B lymphocytes. The molecular mechanisms regulating this response, however, remain incompletely characterized. Activation of the nonreceptor tyrosine kinase, Btk, is essential for CD38 downstream signaling function. The major Btk-dependent substrate in B cells, phospholipase C-gamma2 (PLC-gamma2), functions to generate the key sec...

Journal: :Journal of immunology 2015
James B Case Rachel H Bonami Lindsay E Nyhoff Hannah E Steinberg Allison M Sullivan Peggy L Kendall

Expansion of autoimmune-prone marginal zone (MZ) B cells has been implicated in type 1 diabetes. To test disease contributions of MZ B cells in NOD mice, Notch2 haploinsufficiency (Notch2(+/-)) was introduced but failed to eliminate the MZ, as it does in C57BL/6 mice. Notch2(+/-)/NOD have MZ B cell numbers similar to those of wild-type C57BL/6, yet still develop diabetes. To test whether BCR si...

ژورنال: :مجله دانشگاه علوم پزشکی زنجان 0
سعید ناصری s nasseri رحیم سروری زنجانی r sorouri zanjani زهرا پور پاک z pourpak نیما رضایی n rezaei مصطفی معین m moin نیما پروانه n parvaneh اصغر آقا محمدی

چکیده زمینه و هدف: بیماری آگاماگلوبولینمی وابسته به جنس نوعی نقص ایمنی اولیه بوده که علایم آن شامل عفونت های راجعه ی باکتریایی, کمبود شدید آنتی بادی های سرمی و کاهش لنفوسیت های b خون می باشد. بروز جهش در ژن btk موجب بروز این بیماری می شود. نشان داده شده است که در مواردی عدم بیان پروتئین btk با جهش خاصی در نواحی کدکننده ی ژن همراه نیست و ممکن است در نواحی تنظیمی نظیر پروموتر یا ناحیه ی ابتدایی ا...

2015
Burcu Bestas Janne J. Turunen K. Emelie M. Blomberg Qing Wang Robert Månsson Samir EL Andaloussi Anna Berglöf C. I. Edvard Smith

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disease caused by mutations in the gene coding for Bruton's tyrosine kinase (BTK). Deficiency of BTK leads to a developmental block in B cell differentiation; hence, the patients essentially lack antibody-producing plasma cells and are susceptible to various infections. A substantial portion of the mutations in BTK results in splic...

Journal: :Blood 2007
Klára Sochorová Rudolf Horváth Daniela Rozková Jirí Litzman Jirina Bartunková Anna Sedivá Radek Spísek

The critical role of Bruton tyrosine kinase (Btk) in B cells has been documented by the block of B-cell development in X-linked agammaglobulinemia (XLA). Less is known about Btk function in myeloid cells. Several pieces of evidence indicate that Btk is a component of Toll-like receptor (TLR) signaling. We analyzed whether Btk deficiency in XLA is associated with an impaired dendritic cell (DC) ...

2018
Jon M. Florence Agnieszka Krupa Laela M. Booshehri Adrian L. Gajewski Anna K. Kurdowska

Chronic obstructive pulmonary disease (COPD) is associated with severe chronic inflammation that promotes irreversible tissue destruction. Moreover, the most broadly accepted cause of COPD is exposure to cigarette smoke. There is no effective cure and significantly, the mechanism behind the development and progression of this disease remains unknown. Our laboratory has demonstrated that Bruton'...

Journal: :The Journal of biological chemistry 2001
W E Lowry J Huang M Lei D Rawlings X Y Huang

Defects in Bruton's tyrosine kinase (Btk) are responsible for X chromosome-linked agammaglobulinemia in patients. Mutations in each of the structural domains of Btk have been detected in patients, yet a mechanistic explanation for most of these mutant phenotypes is lacking. To understand the possible role of the unique pleckstrin homology and Tec homology (PHTH) module of Btk, we have compared ...

Journal: :The Journal of pharmacology and experimental therapeutics 2017
Tjeerd Barf Todd Covey Raquel Izumi Bas van de Kar Michael Gulrajani Bart van Lith Maaike van Hoek Edwin de Zwart Diana Mittag Dennis Demont Saskia Verkaik Fanny Krantz Paul G Pearson Roger Ulrich Allard Kaptein

Several small-molecule Bruton tyrosine kinase (BTK) inhibitors are in development for B cell malignancies and autoimmune disorders, each characterized by distinct potency and selectivity patterns. Herein we describe the pharmacologic characterization of BTK inhibitor acalabrutinib [compound 1, ACP-196 (4-[8-amino-3-[(2S)-1-but-2-ynoylpyrrolidin-2-yl]imidazo[1,5-a]pyrazin-1-yl]-N-(2-pyridyl)benz...

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