Rajendran R, Rajeesh Mohammed P K, Shaikh Saleen, Pillai M R
Department of Oral Pathology and Microbiology, Govt Dental College, Kerala.
Indian J Dent Res. 2006 Oct-Dec;17(4):161-6. doi: 10.4103/0970-9290.29870.
Immunohistochemical staining of formalin fixed, paraffin embedded tissue sections of OSF for MMPs-1,2,9 and their tissue inhibitors TIMP-1and 2 was performed using monospecific antibodies coupled with gelatin zymography (MMP-2 and 9) for measuring enzymatic activity quantitatively and for distinguishing the active from the inactive variants of enzymes. The present study, contrary to earlier reports, recorded statistically significant increase in the levels of stromal expression of MMP-1, MMP-2 and MMP-9 and TIMP-1 and TIMP-2 using monospecific antibodies reacting against tissue antigens. The simultaneous increase in reactivity of MMPs and TIMPs poise difficulty in interpretingthe results of this study. The possible reasons for this result, against the backdrop of existing knowledge, were attempted in this study.
使用与明胶酶谱法(用于MMP-2和9)相结合的单特异性抗体,对口腔黏膜下纤维化(OSF)的福尔马林固定、石蜡包埋组织切片进行基质金属蛋白酶(MMPs)-1、2、9及其组织抑制剂TIMP-1和2的免疫组织化学染色,以定量测量酶活性,并区分酶的活性变体和非活性变体。与早期报告相反,本研究使用针对组织抗原的单特异性抗体,记录到MMP-1、MMP-2和MMP-9以及TIMP-1和TIMP-2的基质表达水平有统计学显著增加。MMPs和TIMPs反应性的同时增加给本研究结果的解释带来了困难。在现有知识的背景下,本研究尝试探究这一结果的可能原因。