The Expression of TGF-b1, p38 MAPK, and ERK-1 Protein in Cleft Affected Tissue of the Lip: An Observational Study

H. Y. Wihastyoko, E. P. Sidarta
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Abstract

Background: Cleft lip is a congenital birth defect caused by many proteins. Transforming growth factor (TGF)-β1, p38 mitogen-activated protein kinase (MAPK) and extracellular signal-regulated protein kinase (ERK)-1 are proteins which regulate proliferation and apoptosis role during intrauterine period. This study aimed to observe the expression of these proteins in cleft affected tissue of the lip.Materials and Methods: A descriptive study by examining the TGF-β1, p38 MAPK, and ERK-1 immunohistochemical expression of cleft affected tissue of the lip was conducted. Subjects were patients that were participating for the social event held by Plastic Surgery Department, Faculty of Medicine, Univesitas Brawijaya, on December 3-12, 2012 in Nusa Tenggara Timur. Excess lip mucosa (waste tissue) during the operation were stored in 10% formalin then stained by immunohistochemistry for TGF-β1, p38 MAPK, and ERK-1. We counted the average protein expression under the light microscope with 1000x magnification for 20 different fields of view, randomly.Results: Paraffin blocks from 30 subjects were selected. The mean p38 MAPK expression was found to be highest, with the average of 8 per field of view; followed by the mean TGF-β1 expression, with the average of 5 per field of view; and the mean ERK-1 expression was found to be the lowest, with the average of 2 per field of view. Conclusion: Expression of p38 MAPK and TGF-β1 are higher than ERK-1, suggesting that p38 MAPK is in the same signalling pathway as TGF-β1, while ERK-1 is lower, as its role as anti-apoptotic. This is consistent with several previous studies showing that all proteins took part in the development of cleft lip or craniofacial development. Further study needs to be conducted to determine which protein plays the bigger role.Keywords: cleft lip, TGF-β1, p38 MAPK, ERK-1
TGF-b1、p38 MAPK和ERK-1蛋白在唇裂组织中的表达:一项观察性研究
背景:唇裂是一种由多种蛋白质引起的先天性先天性缺陷。转化生长因子(TGF)-β1、p38丝裂原活化蛋白激酶(MAPK)和细胞外信号调节蛋白激酶(ERK)-1是在子宫内调控细胞增殖和细胞凋亡的蛋白。本研究旨在观察这些蛋白在唇部裂损组织中的表达。材料与方法:通过检测唇部裂患组织中TGF-β1、p38 MAPK、ERK-1免疫组化表达进行描述性研究。研究对象为参加2012年12月3日至12日在努沙登加拉木木尔举行的由布拉维贾亚大学医学院整形外科举办的社交活动的患者。术中多余的唇黏膜(废组织)保存在10%福尔马林中,免疫组织化学染色TGF-β1、p38 MAPK和ERK-1。随机选取20个不同视场,在1000倍放大镜下计算平均蛋白表达量。结果:选取了30例受试者的石蜡块。p38 MAPK的平均表达量最高,平均为8个/视场;其次是平均TGF-β1表达量,平均每个视场5个;平均ERK-1表达量最低,平均每视场2个。结论:p38 MAPK和TGF-β1的表达均高于ERK-1,提示p38 MAPK与TGF-β1处于同一信号通路,而ERK-1表达较低,具有抗凋亡作用。这与之前的几项研究一致,表明所有蛋白质都参与了唇裂或颅面发育的发展。需要进一步的研究来确定哪种蛋白质发挥更大的作用。关键词:唇裂,TGF-β1, p38 MAPK, ERK-1
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