Chait A, Iverius P H, Brunzell J D
J Clin Invest. 1982 Feb;69(2):490-3. doi: 10.1172/jci110473.
Human monocyte-derived macrophages in culture produced lipoprotein lipase. Although freshly isolated blood monocytes did not secrete much lipase activity, 1 d in culture was sufficient to trigger measureable enzyme production. During 3 wk in culture, maximal activity was attained after 7 d. At all times, the culture medium contained more enzyme activity than did a serum-heparin eluate or a detergent extract of the cell layer. The lipase activity was stimulated by serum and was inhibited by preincubation with antiserum to bovine lipoprotein lipase or when assayed at a high salt concentration. Furthermore, the enzyme bound to a heparin-Sepharose affinity column at physiological ionic strength. Cells cultured from a subject with primary lipoprotein lipase deficiency secreted no detectable enzyme. Since macrophages are prominent components of atherosclerotic lesions in man, their ability to synthesize and secrete lipoprotein lipase may be important to atherogenesis.
培养的人单核细胞衍生巨噬细胞可产生脂蛋白脂肪酶。尽管新鲜分离的血液单核细胞分泌的脂肪酶活性不多,但培养1天就足以引发可测量的酶产生。在培养3周期间,7天后达到最大活性。在所有时间点,培养基中的酶活性均高于血清 - 肝素洗脱液或细胞层的去污剂提取物。脂肪酶活性受血清刺激,并在与抗牛脂蛋白脂肪酶抗血清预孵育或在高盐浓度下测定时受到抑制。此外,该酶在生理离子强度下可与肝素 - 琼脂糖亲和柱结合。从原发性脂蛋白脂肪酶缺乏症患者培养的细胞不分泌可检测到的酶。由于巨噬细胞是人类动脉粥样硬化病变的主要成分,它们合成和分泌脂蛋白脂肪酶的能力可能对动脉粥样硬化的发生很重要。