Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Contact of Jurkat T-lymphocytes with the extracellular matrix (ECM) protein laminin resulted in long-lasting alpha6beta1-integrin-mediated Ca(2+) signalling. Both Ca(2+) release from thapsigargin-sensitive Ca(2+) stores and capacitative Ca(2+) entry via Ca(2+) channels sensitive to SKF 96365 constitute important parts of this process. Inhibition of alpha6beta1-integrin-mediated Ca(2+) signalling by (1) the src kinase inhibitor PP2, (2) the PLC inhibitor U73122, and (3) the cyclic adenosine diphosphoribose (cADPR) antagonist 7-deaza-8-Br-cADPR indicate the involvement of src tyrosine kinases and the Ca(2+)-releasing second messengers D-myo-inositol 1,4,5-trisphosphate (InsP3) and cADPR.

Type

Journal article

Journal

Cell Signal

Publication Date

12/2001

Volume

13

Pages

895 - 899

Keywords

Adenosine Diphosphate Ribose, Calcium Channel Blockers, Calcium Signaling, Cyclic ADP-Ribose, Dose-Response Relationship, Drug, Enzyme Inhibitors, Estrenes, Humans, Imidazoles, Integrin alpha6beta1, Integrins, Jurkat Cells, Kinetics, Laminin, Pyrimidines, Pyrrolidinones, T-Lymphocytes, Thapsigargin, Type C Phospholipases, src-Family Kinases