Uncovering the Role of the Hsp40 Family Member, Cysteine String Protein-α, in Mouse Platelets Open Access

• Mice lacking CSPα/DNAJC5/CLN4 have defective granule secretion and thrombosis.

• Deletion of CSPα affected megakaryocytes and increased collagen I deposition in the bone marrow.

Platelets modulate vascular microenvironments via the release of cargo molecules. Granule secretion is modulated by proteins called Soluble NSF Attachment Protein Receptors (SNAREs). Secretion is complex and regulated by several protein-protein interactions; however, not all are characterized in platelets. We have identified Cysteine String Protein-α (CSPα; aka, DNAJC5 or CLN4) as required for platelet secretion. CSPα is the only member from the CSP family present in platelets and has been proposed as a chaperone for the SNAP-23/25 t (Qb,c)-SNAREs. To address CSPα's role, we analyzed platelets from CSPα-/- mice. The loss of CSPα significantly affected dense- and α-granule release with minimal effects on lysosomal secretion. Consistent with the secretion defects, in vivo and ex vivo assays showed that loss of CSPα caused significant bleeding and attenuated thrombosis under flow. Interestingly, loss of CSPα caused a reduction in GPVI levels and reduced αIIbβ3 activation, especially in response to GPVI-specific agonists. Deletion of CSPα did not affect proteins in the platelet secretory machinery, e.g., the SNAP-23/25 proteins. Subcellular fractionation studies showed that CSPα, which is reported to be acylated, was present on membranes but not in lipid rafts. Immunofluorescence studies showed CSPα co-localized with α and lysosomal granules markers. CSPα-/- mice had reduced red blood cell, leukocyte, and megakaryocyte numbers, suggesting effects on bone marrow progenitor cells. Simultaneously, we detected increased collagen I deposition, but no fibrosis in the marrow of CSPα-/- mice. These results identify CSPα as another element of the platelet secretory machinery that significantly contributes to thrombosis and hemostasis.