Background and Purpose: Platelet function during inflammation is dependent on activation by endogenous nucleotides acting on purinergic receptors. The P2Y14 receptor (P2Y14R) has been reported to be expressed on platelets and is involved in leukocyte recruitment during inflammation. However, a role for P2Y14R receptors on platelet function has not yet been determined. Experimental Approach: Platelets obtained from healthy human volunteers were incubated with the P2Y14R agonist, UDP-Glucose (UDP-G), and PPTN, a selective P2Y14R antagonist. Platelet activation was quantified using Ca2+ mobilization, aggregation, and chemotaxis assays. Cooperativity with P2Y1 receptor (P2Y1R) activation was also assessed after stimulation with UDP-G in the presence of MRS2500, a selective P2Y1R antagonist. Key Results: Ca2+ mobilization occurred in platelets after incubation with UDP-G in a concentration-dependent manner, and this was suppressed in platelets treated with PPTN. Platelets did not aggregate, or bind to fibrinogen after incubation with UDP-G. However, platelet chemotaxis towards f-MLP was dependent on P2Y14R stimulation with UDP-G and this was reduced by Rho-GTPase inhibitors. Furthermore, UDP-G induced Ca2+ mobilization and chemotaxis were also inhibited when platelets were pretreated with MRS2500. Conversely, ADP induced Ca2+ mobilization, chemotaxis and aggregation were not affected by the incubation with PPTN. Conclusion and Implications: Platelets can be activated via P2Y14R stimulation to induce chemotaxis but not aggregation. Furthermore, this was dependent on concomitant activation of P2Y1R. Activation of P2Y14Rs on platelets may therefore be relevant during inflammation, but cooperation with P2Y1R activation is required.