Brody I
Ups J Med Sci. 1986;91(1):1-16. doi: 10.3109/03009738609178486.
Mast cell degranulation (MCD) was studied in lesions of chronic psoriasis vulgaris before and during topical treatment with low-strength anthralin. Before the treatment, two forms (A and B) of mast cells with Type I MCD were distinguished in the lesions, in addition to mast cells showing Type II MCD. In Type I MCD, electron-dense mast cell granules in form A mast cells, and electron-dense mast cell granules and vacuoles containing granule matrix in form B mast cells, were released as intact structures by the mechanism of diacytosis. Distinct gaps of the mast cell plasma membranes were observed. Around blood vessels, beneath the epidermal-dermal junction and in the intercellular space of strata basale and spinosum, the mast cell granules appeared partly as intact structures and partly in more or less disintegrated form. In Type II MCD the granule matrix was released into the extracellular compartment by the mechanism of exocytosis. During treatment with low-strength anthralin, the mast cell changes underwent regression. In macular psoriasis only form A mast cells of Type I MCD were demonstrated, and the released intact mast cell granules were restricted to the immediate neighbourhood of the mast cells. There were no mast cell granules in the epidermis. At the sites with clinically complete clearance of psoriatic lesions, the mast cells displayed no degranulation but distinct gaps were still found in the mast cell plasma membranes. Low-strength anthralin's mode of action in psoriasis is suggested to involve regression of a series of systems, including prevention of mast cell degranulation, thereby inhibiting release of histamine, proteinase and other mast cell mediators sustaining the psoriatic process.
在寻常型慢性银屑病皮损中,于外用低浓度蒽林治疗前及治疗期间对肥大细胞脱颗粒(MCD)进行了研究。治疗前,除了显示II型MCD的肥大细胞外,在皮损中还区分出了具有I型MCD的两种肥大细胞形式(A和B)。在I型MCD中,A 型肥大细胞中电子致密的肥大细胞颗粒,以及B型肥大细胞中电子致密的肥大细胞颗粒和含有颗粒基质的空泡,通过双胞吐作用机制作为完整结构释放。观察到肥大细胞质膜有明显间隙。在血管周围、表皮-真皮交界处下方以及基底层和棘层的细胞间隙中,肥大细胞颗粒部分呈现为完整结构,部分呈现为或多或少的解体形式。在II型MCD中,颗粒基质通过胞吐作用机制释放到细胞外间隙。在用低浓度蒽林治疗期间,肥大细胞的变化逐渐消退。在点滴状银屑病中,仅显示出I型MCD的A型肥大细胞,释放的完整肥大细胞颗粒局限于肥大细胞紧邻区域。表皮中没有肥大细胞颗粒。在银屑病皮损临床完全清除的部位,肥大细胞未显示脱颗粒,但在肥大细胞质膜中仍发现明显间隙。低浓度蒽林在银屑病中的作用方式被认为涉及一系列系统的消退,包括预防肥大细胞脱颗粒,从而抑制组胺、蛋白酶和其他维持银屑病进程的肥大细胞介质的释放。