Zani Marcelo B, Sant'Ana Aquiles M, Tognato Rafael C, Chagas Jair R, Puzer Luciano
Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Sao Bernardo do Campo, Brazil.
Departamento de Biofísica, Universidade Federal de São Paulo, São Paulo, Brazil.
Front Med (Lausanne). 2022 Mar 4;8:777619. doi: 10.3389/fmed.2021.777619. eCollection 2021.
Human tissue Kallikrein-related peptidases (hKLKs) are serine proteases distributed in several tissues that are involved in several biological processes. In skin, many are responsible for skin desquamation in the Stratum Corneum (SC) of the epidermis, specially hKLK5, hKLK7, hKLK6, hKLK8, and hKLK14. In SC, hKLKs cleave proteins of corneodesmosomes, an important structure responsible to maintain corneocytes attached. As part of skin desquamation, hKLKs are also involved in skin diseases with abnormal desquamation and inflammation, such as Atopic Dermatitis (AD), psoriasis, and the rare disease Netherton Syndrome (NS). Many studies point to hKLK overexpression or overactive in skin diseases, and they are also part of the natural skin inflammation process, through the PAR2 cleavage pathway. Therefore, the control of hKLK activity may offer successful treatments for skin diseases, improving the quality of life in patients. Diseases like AD, Psoriasis, and NS have an impact on social life, causing pain, itchy and mental disorders. In this review, we address the molecular mechanisms of skin desquamation, emphasizing the roles of human tissue Kallikrein-related peptidases, and the promising therapies targeting the inhibition of hKLKs.
人组织激肽释放酶相关肽酶(hKLKs)是分布于多种组织中的丝氨酸蛋白酶,参与多种生物学过程。在皮肤中,许多hKLKs负责表皮角质层(SC)的皮肤脱屑,特别是hKLK5、hKLK7、hKLK6、hKLK8和hKLK14。在SC中,hKLKs切割桥粒芯蛋白,桥粒芯蛋白是维持角质形成细胞附着的重要结构。作为皮肤脱屑的一部分,hKLKs还参与脱屑和炎症异常的皮肤疾病,如特应性皮炎(AD)、银屑病和罕见的Netherton综合征(NS)。许多研究指出hKLKs在皮肤疾病中过表达或过度活跃,并且它们也是天然皮肤炎症过程的一部分,通过蛋白酶激活受体2(PAR2)裂解途径。因此,控制hKLK活性可能为皮肤疾病提供成功的治疗方法,改善患者的生活质量。AD、银屑病和NS等疾病会影响社会生活,导致疼痛、瘙痒和精神障碍。在这篇综述中,我们阐述了皮肤脱屑的分子机制,强调了人组织激肽释放酶相关肽酶的作用,以及针对hKLKs抑制的有前景的治疗方法。