Unit of Dermatology and Venereology, Department of Medicine, Karolinska University Hospital, Solna, Stockholm 171 76, Sweden.
Arch Dermatol Res. 2009 Jul;301(6):449-57. doi: 10.1007/s00403-009-0933-y. Epub 2009 Mar 5.
Since the symptoms of psoriasis may be changed by treatment with selective serotonin reuptake inhibitors (SSRIs), the expression of serotonin (5-HT) and its transporter protein (SERT) in the skin of patients with psoriasis were examined employing a biotinylated-streptavidine procedure. In biopsies of such skin staining for 5-HT was limited to platelets; the expression of SERT in the keratinocytes of involved regions was redistributed; the numbers of SERT-positive dendritic or round mononuclear cells in the epidermis of involved psoriatic skin were higher than in normal healthy control skin; and the dermis of the involved skin contained higher numbers of round inflammatory cells immunostained for SERT than either non-involved psoriatic skin or normal skin. Double-immunostaining indicated that the skin cells expressing SERT also expressed CD1a, CD3 or tryptase. In addition, SERT immunostaining was co localized with caspase-3, a key regulator of apoptosis, but not with TUNEL staining. The present findings indicate that SERT might play a role in regulating apoptosis in inflammatory cells associated with psoriasis, in which case this protein might constitute a valuable therapeutic target.
由于选择性 5-羟色胺再摄取抑制剂(SSRIs)治疗可能改变银屑病的症状,因此检查了银屑病患者皮肤中 5-羟色胺(5-HT)及其转运蛋白(SERT)的表达。采用生物素化链霉亲和素法,对皮肤活检标本进行 5-HT 染色,结果显示血小板染色阳性;SERT 在受累区域角质形成细胞中的表达重新分布;银屑病皮损表皮中 SERT 阳性树突状或圆形单核细胞数量高于正常健康对照皮肤;受累皮肤的真皮中,SERT 免疫染色的圆形炎症细胞数量高于非受累银屑病皮肤或正常皮肤。双免疫染色表明,表达 SERT 的皮肤细胞也表达 CD1a、CD3 或类胰蛋白酶。此外,SERT 免疫染色与凋亡的关键调节因子 caspase-3 共定位,但与 TUNEL 染色不共定位。这些发现表明,SERT 可能在调节与银屑病相关的炎症细胞凋亡中发挥作用,在这种情况下,该蛋白可能构成一个有价值的治疗靶点。