Hatanaka K, Li X A, Guo L, Sakata T, Gillissen J A, Yoshioka A, Yamamoto A
Department of Etiology/Pathophysiology, National Cardiovascular Center, Osaka, Japan.
Thromb Res. 1994 Jun 15;74(6):643-54. doi: 10.1016/0049-3848(94)90220-8.
We have experienced a coagulation factor VIII-deficient patient whose plasma has normal protein S (PS) activity and masses of free PS and its bound form in complex with C4b-binding protein (C4BP). Although the patient's plasma showed a normal ratio of free PS to PS-C4BP complex in the presence of 5 mM EDTA, the plasma gave an abnormally retarding major C4BP peak together with a major PS peak in the crossed immunoelectrophoresis (CIE) in the presence of 2 mM CaCl2. It was revealed that the major peak was formed by a mixture of PS-C4BP complex and free form. The addition of normal human plasma (NHP) to the patient's plasma inhibited the retardation of the major PS-C4BP complex. These suggest that the patient's plasma lacks some component(s) to inhibit Ca(2+)-dependent association of PS with C4BP.