Literature DB >> 12220673

Silencing of Bruton's tyrosine kinase (Btk) using short interfering RNA duplexes (siRNA).

Juhana E Heinonen1, C I Edvard Smith, Beston F Nore.   

Abstract

Tec family tyrosine kinases, Bruton's tyrosine kinase (Btk), Itk, Bmx, Tec, and Txk, are multi-domain proteins involved in hematopoietic signaling. Here, we demonstrate that human Btk protein can transiently be depleted using double-stranded short RNA interference (siRNA) oligonucleotides. Imaging and Western blotting analysis demonstrate that Btk expression is down regulated in heterologous systems as well as in hematopoietic lineages, following transfection or microinjection of Btk siRNA duplexes. The induction of histamine release, a pro-inflammatory mediator, in RBL-2H3 mast cells was reduced by 20-25% upon Btk down regulation. Similar, results were obtained when the Btk activity was inhibited using the kinase blocker LFM-A13. These results demonstrate a direct role of Btk for the efficient secretion of histamine in allergic responses.

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Year:  2002        PMID: 12220673     DOI: 10.1016/s0014-5793(02)03206-4

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  12 in total

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3.  A multitude of kinases--which are the best targets in treating rheumatoid arthritis?

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Review 5.  The tyrosine kinase network regulating mast cell activation.

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6.  Btk Inhibitor RN983 Delivered by Dry Powder Nose-only Aerosol Inhalation Inhibits Bronchoconstriction and Pulmonary Inflammation in the Ovalbumin Allergic Mouse Model of Asthma.

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7.  Dual phosphorylation of Btk by Akt/protein kinase b provides docking for 14-3-3ζ, regulates shuttling, and attenuates both tonic and induced signaling in B cells.

Authors:  Dara K Mohammad; Beston F Nore; Alamdar Hussain; Manuela O Gustafsson; Abdalla J Mohamed; C I Edvard Smith
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Review 8.  Immunological research using RNA interference technology.

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9.  A review of antisense therapeutic interventions for molecular biological targets in asthma.

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10.  Novel Bruton's tyrosine kinase inhibitors currently in development.

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