Reusch M K, Wastek G J
Department of Dermatology, Stanford University School of Medicine, CA.
Acta Derm Venereol. 1989;69(5):429-31.
We have demonstrated a high-affinity binding site for leukotriene B4 (LTB4) on human epidermal keratinocytes in vitro. In substrate saturation studies, one population of binding sites with a dissociation constant (Kd) of 1.03 +/- 0.3 nM and a maximal binding capacity (Bmax) of 148.2 +/- 45.3 fmol/mg protein could be demonstrated. On average 5,500 binding sites were found on individual keratinocytes in culture. The affinity constant of this binding site correlates well with previous reports on the proliferative effect of LTB4 on keratinocytes in vitro. These findings confirm that LTB4 may in part be responsible for epidermal hyperproliferation in inflammatory skin diseases.
我们已经在体外证明了人表皮角质形成细胞上存在白三烯B4(LTB4)的高亲和力结合位点。在底物饱和研究中,可以证明存在一类结合位点,其解离常数(Kd)为1.03±0.3 nM,最大结合容量(Bmax)为148.2±45.3 fmol/mg蛋白质。在培养的单个角质形成细胞上平均发现5500个结合位点。该结合位点的亲和常数与先前关于LTB4对角质形成细胞体外增殖作用的报道密切相关。这些发现证实,LTB4可能部分导致炎症性皮肤病中的表皮过度增殖。