Muller A, Michel L, Basset-Seguin N, Modat G, Dubertret L, Bonne C
Laboratoire de Physiologie Cellulaire, Université Montpellier 1, France.
Br J Dermatol. 1988 Sep;119(3):275-80. doi: 10.1111/j.1365-2133.1988.tb03218.x.
Peptidoleukotriene C4 (LTC4) and leukotriene B4 (LTB4) are both suspected of being inflammatory mediators and epidermal mitogenic agents in cutaneous psoriatic lesions. In the present study an LTC4 specific binding site was characterized in membranes from cultured human keratinocytes (Kd, 8.7 nmol/l; Bmax, 1.2 pmol/mg protein). In contrast LTB4 did not show any high affinity binding which could account for its biological effects. These data suggest that LTC4, unlike LTB4, acts on epidermal cells through a receptor-mediated mechanism.
肽白三烯C4(LTC4)和白三烯B4(LTB4)均被怀疑是皮肤银屑病皮损中的炎症介质和表皮促有丝分裂剂。在本研究中,在培养的人角质形成细胞膜中鉴定出了LTC4特异性结合位点(解离常数Kd为8.7 nmol/l;最大结合容量Bmax为1.2 pmol/mg蛋白质)。相比之下,LTB4未显示出任何可解释其生物学效应的高亲和力结合。这些数据表明,与LTB4不同,LTC4通过受体介导的机制作用于表皮细胞。