Shenzhen Eye Hospital, Jinan University, Shenzhen Eye Institute, Shenzhen, China.
Department of Cardiovascular Medicine, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Transl Vis Sci Technol. 2022 Dec 1;11(12):4. doi: 10.1167/tvst.11.12.4.
To screen and compare the differential proteins in meibomian gland secretions between patients with blepharokeratoconjunctivitis (BKC) and healthy individuals and to identify target proteins that may participate in the occurrence and development of BKC.
Thirteen patients diagnosed with BKC in Shenzhen Eye Hospital and five healthy volunteers were included in this study. Meibomian gland secretions and clinical traits were collected before and after 1 month of standard BKC treatment. Label-free mass spectrometry was used for proteomic detection of meibomian gland secretions. Weighted protein coexpression network analysis (WPCNA) and several different protein analyses were performed to identify hub proteins associated with BKC and its clinical characteristics.
Patients with BKC had significantly lower cleanliness of the eyelid margin, higher palpebral margin scores, more serious clinical manifestations of secretions, and more damaged meibomian gland morphology compared with the healthy controls. One hundred fifteen differential proteins were associated with the clinical traits, which included diagnosis, sex, age, severity, corneal neovascularization, disease course, eyelid margin cleanliness, palpebral margin score, secretion characteristics, and meibomian gland morphology. Four hub proteins related to inflammation and the immune response (namely, S100A8, S100A9, ANXA3, and LCN2) were increased in BKC and remained increased after 1 month of treatment. The cleanliness, blepharon eyelid score, and secretion characteristics were improved after BKC treatment.
S100A8, S100A9, ANXA3, and LCN2 are BKC-associated proteins probably involved in the chronic inflammation of BKC.
Hub proteins probably involved in chronic inflammation of BKC were identified by proteomic methods.
筛选和比较睑板腺功能障碍(BKC)患者和健康个体的睑板腺分泌物中的差异蛋白,并鉴定可能参与 BKC 发生和发展的靶蛋白。
本研究纳入了深圳眼科医院 13 名 BKC 患者和 5 名健康志愿者。在标准 BKC 治疗前和治疗 1 个月后收集了睑板腺分泌物和临床特征。使用无标记质谱法进行睑板腺分泌物的蛋白质组学检测。进行加权蛋白质共表达网络分析(WPCNA)和几种不同的蛋白质分析,以鉴定与 BKC 及其临床特征相关的关键蛋白。
与健康对照组相比,BKC 患者的睑缘清洁度显著降低,睑缘评分较高,分泌物的临床表现更严重,睑板腺形态受损更严重。与临床特征相关的 115 个差异蛋白包括诊断、性别、年龄、严重程度、角膜新生血管形成、病程、睑缘清洁度、睑缘评分、分泌物特征和睑板腺形态。与炎症和免疫反应相关的 4 个关键蛋白(即 S100A8、S100A9、ANXA3 和 LCN2)在 BKC 中增加,并在治疗 1 个月后仍保持增加。BKC 治疗后,睑缘清洁度、睑板腺眼睑评分和分泌物特征得到改善。
S100A8、S100A9、ANXA3 和 LCN2 是与 BKC 相关的蛋白,可能参与 BKC 的慢性炎症。
杨宁