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卡氏棘阿米巴的体内和体外胶原酶活性

In vivo and in vitro collagenolytic activity of Acanthamoeba castellanii.

作者信息

He Y G, Niederkorn J Y, McCulley J P, Stewart G L, Meyer D R, Silvany R, Dougherty J

机构信息

Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

Invest Ophthalmol Vis Sci. 1990 Nov;31(11):2235-40.

PMID:2173683
Abstract

Axenic cultures of Acanthamoeba castellanii contained a collagenolytic enzyme that digested collagen shields and purified collagen in vitro. Specificity of biologic activity was determined by the addition of selected enzyme inhibitors to the assays and revealed that the parasite-conditioned medium contained both collagenase and lower concentrations of other proteolytic enzymes. However, most of the collagenolytic and pathogenic activity was directly attributable to specific collagenase. Intrastromal injection of sterile, Acanthamoeba-conditioned culture medium into naive Lewis rats produced corneal lesions clinically similar to and closely resembling those found in biopsy specimens of human patients diagnosed with acanthamoebic keratitis. Histopathologic analysis revealed moderate-to-severe neutrophil infiltration, disruption of stromal lamellae, and edema. Identical pathologic sequelae were produced by intrastromal injection of purified collagenase (25 units/ml). The pathogenicity of the soluble parasite-derived product was removed by passage over affinity columns armed with antibody specific for collagenase. These results indicated that soluble parasite-derived factors were capable of producing lesions characteristic of acanthamoebic keratitis and that the pathogenicity of these factors was either directly or indirectly attributable to specific collagenase activity.

摘要

卡氏棘阿米巴的无菌培养物含有一种胶原酶,该酶可在体外消化胶原防护层和纯化的胶原蛋白。通过在检测中添加选定的酶抑制剂来确定生物活性的特异性,结果显示寄生虫条件培养基中既含有胶原酶,也含有较低浓度的其他蛋白水解酶。然而,大部分胶原分解活性和致病活性直接归因于特定的胶原酶。将无菌的、棘阿米巴条件培养基基质内注射到未感染的Lewis大鼠体内,会产生临床上与诊断为棘阿米巴角膜炎的人类患者活检标本中发现的角膜病变相似且极为相像的病变。组织病理学分析显示有中度至重度中性粒细胞浸润、基质板层破坏和水肿。通过基质内注射纯化的胶原酶(25单位/毫升)也会产生相同的病理后果。可溶性寄生虫衍生产物的致病性可通过用装有针对胶原酶的特异性抗体的亲和柱进行过柱处理而消除。这些结果表明,可溶性寄生虫衍生因子能够产生棘阿米巴角膜炎特征性的病变,并且这些因子的致病性直接或间接归因于特定的胶原酶活性。

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