CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation.

Journal:

Nat. Med. 2004 Sep

Authors:

Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM

Abstract

Signaling through the second messengers calcium and diacylglycerol (DAG) is a critical element in many biological systems. Integration of calcium and DAG signals has been suggested to occur primarily through protein kinase C family members, which bind both calcium and DAG. However, an alternative pathway may involve members of the CalDAG-GEF/RasGRP protein family, which have structural features (calcium-binding EF hands and DAG-binding C1 domains) that suggest they can function in calcium and DA
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G signal integration. To gain insight into the signaling systems that may be regulated by CalDAG-GEF/RasGRP family members, we have focused on CalDAG-GEFI, which is expressed preferentially in the brain and blood. Through genetic ablation in the mouse, we have found that CalDAG-GEFI is crucial for signal integration in platelets. Mouse platelets that lack CalDAG-GEFI are severely compromised in integrin-dependent aggregation as a consequence of their inability to signal through CalDAG-GEFI to its target, the small GTPase Rap1. These results suggest that analogous signaling defects are likely to occur in the central nervous system when CalDAG-GEFI is absent or compromised in function.[less]

Mesh Headings:

Animals, Blood Cell Count, Calcium, DNA Primers, DNA-Binding Proteins, Diglycerides, Flow Cytometry, Genotype, Guanine Nucleotide Exchange Factors, Immunohistochemistry, Mice, Mice, Knockout, Platelet Aggregation, Second Messenger Systems, Signal Transduction, Thrombosis, rap1 GTP-Binding Proteins