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马属动物蹄叶炎细菌致病机制的体外证据。

In vitro evidence for a bacterial pathogenesis of equine laminitis.

作者信息

Mungall B A, Kyaw-Tanner M, Pollitt C C

机构信息

Department of Companion Animal Sciences, School of Veterinary Science, The University of Queensland, St. Lucia, Qld 4072, Australia.

出版信息

Vet Microbiol. 2001 Apr 2;79(3):209-23. doi: 10.1016/s0378-1135(00)00359-x.

DOI:10.1016/s0378-1135(00)00359-x
PMID:11240100
Abstract

Utilizing an in vitro laminitis explant model, we have investigated how bacterial broth cultures and purified bacterial proteases activate matrix metalloproteinases (MMPs) and alter structural integrity of cultured equine lamellar hoof explants. Four Gram-positive Streptococcus spp. and three Gram-negative bacteria all induced a dose-dependent activation of MMP-2 and MMP-9 and caused lamellar explants to separate. MMP activation was deemed to have occurred if a specific MMP inhibitor, batimastat, blocked MMP activity and prevented lamellar separation. Thermolysin and streptococcal pyrogenic exotoxin B (SpeB) both separated explants dose-dependently but only thermolysin was inhibitable by batimastat or induced MMP activation equivalent to that seen with bacterial broths. Additionally, thermolysin and broth MMP activation appeared to be cell dependent as MMP activation did not occur in isolation. These results suggest the rapid increase in streptococcal species in the caecum and colon observed in parallel with carbohydrate induced equine laminitis may directly cause laminitis via production of exotoxin(s) capable of activating resident MMPs within the lamellar structure. Once activated, these MMPs can degrade key components of the basement membrane (BM) hemidesmosome complex, ultimately separating the BM from the epidermal basal cells resulting in the characteristic laminitis histopathology of hoof lamellae. While many different causative agents have been evaluated in the past, the results of this study provide a unifying aetiological mechanism for the development of carbohydrate induced equine laminitis.

摘要

利用体外蹄叶炎外植体模型,我们研究了细菌肉汤培养物和纯化的细菌蛋白酶如何激活基质金属蛋白酶(MMPs)并改变培养的马属动物蹄叶外植体的结构完整性。四种革兰氏阳性链球菌属细菌和三种革兰氏阴性细菌均诱导了MMP-2和MMP-9的剂量依赖性激活,并导致蹄叶外植体分离。如果一种特异性MMP抑制剂batimastat能阻断MMP活性并防止蹄叶分离,则认为发生了MMP激活。嗜热菌蛋白酶和链球菌致热外毒素B(SpeB)均能剂量依赖性地使外植体分离,但只有嗜热菌蛋白酶可被batimastat抑制或诱导出与细菌肉汤所见相当的MMP激活。此外,嗜热菌蛋白酶和肉汤诱导的MMP激活似乎依赖于细胞,因为单独时不会发生MMP激活。这些结果表明,在碳水化合物诱导的马属动物蹄叶炎中观察到的盲肠和结肠中链球菌种类的快速增加,可能通过产生能够激活蹄叶结构内常驻MMPs的外毒素而直接导致蹄叶炎。一旦被激活,这些MMPs可降解基底膜(BM)半桥粒复合物的关键成分,最终使BM与表皮基底细胞分离,导致蹄叶典型的蹄叶炎组织病理学变化。虽然过去已经评估了许多不同的致病因素,但本研究结果为碳水化合物诱导的马属动物蹄叶炎的发展提供了一个统一的病因机制。

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