Kyaw-Tanner M, Pollitt C C
Australian Equine Laminitis Research Unit, School of Veterinary Science, Faculty of Natural Resources Agriculture and Veterinary Science, The University of Queensland, Brisbane, Queensland 4072, Australia.
Equine Vet J. 2004 Apr;36(3):221-5. doi: 10.2746/0425164044877242.
The dysadhesion and destruction of lamellar basement membrane of laminitis may be due to increased lamellar metalloproteinase activity. Characterising lamellar metalloproteinase-2 (MMP-2) and locating it in lamellar tissues may help determine if laminitis pathology is associated with increased MMP-2 transcription.
To clone and sequence the cDNA encoding lamellar MMP-2, develop antibody and in situ hybridisation probes to locate lamellar MMP-2 and quantitate MMP-2 transcription in normal and laminitis tissue.
Total RNA was isolated, fragmented by RT-PCR, cloned into vector and sequenced. Rabbit anti-equine MMP-2 and labelled MMP-2 riboprobe were developed to analyse and quantitate MMP-2 expression.
Western immunoblotting with anti-MMP-2 detected 72 kDa MMP-2 in hoof tissue homogenates and cross-reacted with human MMP-2. Immunohistochemistry and in situ hybridisation detected MMP-2 in the cytoplasm of basal and parabasal cells in close proximity to the lamellar basement membrane. Northern analysis and quantitative real-time PCR showed MMP-2 expression significantly (P < 0.01) elevated in laminitis affected tissues.
The lamellar pathology of laminitis is associated with increased transcription of MMP-2.
Real-time PCR analysis of lamellar MMP-2 accurately monitors laminitis development at the molecular level and can be used diagnostically and for testing preventive strategies. Controlling increased MMP-2 transcription may ameliorate or prevent laminitis in high risk clinical situations. Our findings represent a warning to clinicians that the basement membrane lesion of laminitis is insidious and well under way before clinical signs are apparent.
蹄叶炎中板层基底膜的黏附障碍和破坏可能是由于板层金属蛋白酶活性增加所致。对板层金属蛋白酶-2(MMP-2)进行特性鉴定并确定其在板层组织中的定位,可能有助于确定蹄叶炎病理是否与MMP-2转录增加有关。
克隆并测序编码板层MMP-2的cDNA,制备抗体和原位杂交探针以定位板层MMP-2,并定量正常和蹄叶炎组织中MMP-2的转录。
提取总RNA,通过逆转录聚合酶链反应(RT-PCR)进行片段化,克隆到载体中并测序。制备兔抗马MMP-2抗体和标记的MMP-2核糖探针,以分析和定量MMP-2的表达。
用抗MMP-2进行的蛋白质免疫印迹法在蹄组织匀浆中检测到72 kDa的MMP-2,并且与人MMP-2发生交叉反应。免疫组织化学和原位杂交在紧邻板层基底膜的基底细胞和副基底细胞的细胞质中检测到MMP-2。Northern印迹分析和定量实时PCR显示,在患蹄叶炎的组织中MMP-2表达显著升高(P < 0.01)。
蹄叶炎的板层病理与MMP-2转录增加有关。
对板层MMP-2进行实时PCR分析可在分子水平准确监测蹄叶炎的发展,可用于诊断和测试预防策略。控制MMP-2转录增加可能改善或预防高风险临床情况下的蹄叶炎。我们的研究结果向临床医生发出警告,即蹄叶炎的基底膜病变在临床症状出现之前就已悄然发生且进展良好。