This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dobenecker, M.-W.
Right arrow Articles by Tarakhovsky, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dobenecker, M.-W.
Right arrow Articles by Tarakhovsky, A.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, December 2005, p. 10533-10542, Vol. 25, No. 23
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.23.10533-10542.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

The Ubiquitously Expressed Csk Adaptor Protein Cbp Is Dispensable for Embryogenesis and T-Cell Development and Function

Marc-Werner Dobenecker,1* Christian Schmedt,1,{dagger} Masato Okada,2 and Alexander Tarakhovsky1*

Laboratory of Lymphocyte Signaling, The Rockefeller University, 1230 York Avenue, New York, New York 10021,1 Department of Oncogene Research, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan2

Received 26 August 2005/ Accepted 15 September 2005

Regulation of Src family kinase (SFK) activity is indispensable for a functional immune system and embryogenesis. The activity of SFKs is inhibited by the presence of the carboxy-terminal Src kinase (Csk) at the cell membrane. Thus, recruitment of cytosolic Csk to the membrane-associated SFKs is crucial for its regulatory function. Previous studies utilizing in vitro and transgenic models suggested that the Csk-binding protein (Cbp), also known as phosphoprotein associated with glycosphingolipid microdomains (PAG), is the membrane adaptor for Csk. However, loss-of-function genetic evidence to support this notion was lacking. Herein, we demonstrate that the targeted disruption of the cbp gene in mice has no effect on embryogenesis, thymic development, or T-cell functions in vivo. Moreover, recruitment of Csk to the specialized membrane compartment of "lipid rafts" is not impaired by Cbp deficiency. Our results indicate that Cbp is dispensable for the recruitment of Csk to the membrane and that another Csk adaptor, yet to be discovered, compensates for the loss of Cbp.


* Corresponding author. Mailing address: Laboratory of Lymphocyte Signaling, The Rockefeller University, 1230 York Avenue, Box 301, New York, NY 10021. Phone: (212) 327-8256. Fax: (212) 327-8258. E-mail for Marc-Werner Dobenecker: dobenem{at}mail.rockefeller.edu. E-mail for Alexander Tarakhovsky: tarakho{at}mail.rockefeller.edu.

{dagger} Current address: Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA 92121.


Molecular and Cellular Biology, December 2005, p. 10533-10542, Vol. 25, No. 23
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.23.10533-10542.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Tauzin, S., Ding, H., Khatib, K., Ahmad, I., Burdevet, D., van Echten-Deckert, G., Lindquist, J. A., Schraven, B., Din, N.-u., Borisch, B., Hoessli, D. C. (2008). Oncogenic association of the Cbp/PAG adaptor protein with the Lyn tyrosine kinase in human B-NHL rafts. Blood 111: 2310-2320 [Abstract] [Full Text]  
  • Ruppelt, A., Mosenden, R., Gronholm, M., Aandahl, E. M., Tobin, D., Carlson, C. R., Abrahamsen, H., Herberg, F. W., Carpen, O., Tasken, K. (2007). Inhibition of T Cell Activation by Cyclic Adenosine 5'-Monophosphate Requires Lipid Raft Targeting of Protein Kinase A Type I by the A-Kinase Anchoring Protein Ezrin. J. Immunol. 179: 5159-5168 [Abstract] [Full Text]  
  • Filby, A., Seddon, B., Kleczkowska, J., Salmond, R., Tomlinson, P., Smida, M., Lindquist, J. A., Schraven, B., Zamoyska, R. (2007). Fyn Regulates the Duration of TCR Engagement Needed for Commitment to Effector Function. J. Immunol. 179: 4635-4644 [Abstract] [Full Text]  
  • Smida, M., Posevitz-Fejfar, A., Horejsi, V., Schraven, B., Lindquist, J. A. (2007). A novel negative regulatory function of the phosphoprotein associated with glycosphingolipid-enriched microdomains: blocking Ras activation. Blood 110: 596-625 [Abstract] [Full Text]  
  • Davidson, D., Schraven, B., Veillette, A. (2007). PAG-Associated FynT Regulates Calcium Signaling and Promotes Anergy in T Lymphocytes. Mol. Cell. Biol. 27: 1960-1973 [Abstract] [Full Text]  
  • Kitaura, J., Kawakami, Y., Maeda-Yamamoto, M., Horejsi, V., Kawakami, T. (2007). Dysregulation of Src Family Kinases in Mast Cells from Epilepsy-Resistant ASK versus Epilepsy-Prone EL Mice. J. Immunol. 178: 455-462 [Abstract] [Full Text]  
  • Patke, A., Mecklenbrauker, I., Erdjument-Bromage, H., Tempst, P., Tarakhovsky, A. (2006). BAFF controls B cell metabolic fitness through a PKC{beta}- and Akt-dependent mechanism. JEM 203: 2551-2562 [Abstract] [Full Text]