Binding of human serum amyloid P component (hSAP) to human neutrophils

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Abstract
Human serum amyloid P component (hSAP) and human C‐reactive protein (hCRP) are normal serum constituents related to the pentraxin family of plasma proteins. hSAP has morphological and immunochemical identity and extensive sequence similarity to the amyloid P (AP) component found in normal tissues and particularly in amyloid deposits. hCRP and its proteolytic products have been previously shown to bind and to interact with various types of human leukocytes. Binding‐displacement experiments with 125I‐labeled hSAP and hCRP show that both proteins have specific high‐affinity binding sites on normal human polymorphonuclear leukocytes (PMN) and each can compete efficiently with the binding of the other. Scatchard analysis of hSAP‐displacement curves reveals a heterogeneous population of hSAP‐binding sites existing on the PMN cells, among them about 300000 low‐affinity binding sites with Kd≤ 5X10−6 M and about 30000 high‐affinity binding sites with Kd≤ 5X10−8 M. hAP was found to be degraded by enzymes from human neutrophils to yield a mixture of low‐molecular‐mass peptides, similarly to the case of CRP reported previously. The binding of hSAP can be efficiently inhibited by this peptide mixture. The results suggest that both hCRP and hSAP, together with related peptides, may participate in vivo in an unknown mechanism of regulation of human neutrophils.

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