b-D-Glucans are major structural components of the fungal cell wall and mainly consist of (1→3)-linked and (1→6)-linked b-D-glucopyranosyl residues.1,2) The ratio of (1→3)-/ (1→6)-linkages and architecture of the b-glucan network vary significantly depending on the species as well as specimens, such as from mycelium, fruit body, and yeast. It is well known that fungal (1→3)-b-D-glucans exhibit various immunomodulating activities, such as antitumor activity, adjuvant activity, hematopoietic activity, complement activation, and cytokine production. [3][4][5][6][7][8] We have been studying the relationship between the structure and activity of fungal b-glucans and suggested that the activity of b-glucan was significantly different depending on the molecular weight, degree of branching, solubility, and conformation. Even though bglucans are the major component of the fungal cell wall, the structure and content of immunomodulating b-glucans are also significantly different depending on the species and specimens. It is difficult to discriminate between the immunomodulating versus inert b-glucans in fungi, and b-glucans may show a variety of immunomodulating spectra. On the other hand, (1→3)-b-D-glucans are detected in the sera of patients with systemic fungal infections and are clinically approved for the diagnostic limulus G test. 9) Recently, several investigators have suggested the presence of the b-glucan receptor on human monocytes and murine peritoneal macrophages, and these proteins could be candidates for the functional b-glucan receptor.10-12) However, this is not sufficient to understand the entire mechanism of b-glucan mediated biological activity because of the diversity of b-glucanmediated activity.Platelets are anucleate blood cells that are required for hemostasis and they participate in pathologic thrombotic syndromes. Platelets are one of the primary defense barriers against the invasion of bacteria and fungi and are important for the induction of inflammatory responses, mediated mainly by preformed granular components such as chemokines, cytokines, growth factors, and microbicidal proteins. 16) It was also demonstrated that this process continues for hours after stimulation with thrombinor integrin-mediated adhesion. It was also reported that human platelets bind to phagocytes via P-selectin and P-selectin glycoprotein ligand-1 (PSGL-1) and modulate the function of these cells, i.e., by cytokine production, superoxide anion production, etc. [17][18][19][20] Elstad et al. suggested that P-selectin primes monocytes for increased platelet-activating factor (PAF) synthesis through regulation of the b-glucan receptor or regulation of signal transduction mechanisms that are linked to the receptor, and that P-selectin expressed on endothelial cells or platelets may serve both to localize monocytes at sites of vascular inflammation or thrombosis and to prime the cells for subsequent responses to augment inflammation. Recently, we have demonstrated that human leukocytes as well as cell lines were activated in...