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马属动物蹄叶炎:葡萄糖剥夺和基质金属蛋白酶激活在体外诱导真皮-表皮分离。

Equine laminitis: glucose deprivation and MMP activation induce dermo-epidermal separation in vitro.

作者信息

French K R, Pollitt C C

机构信息

Australian Equine Laminitis Research Unit, School of Veterinary Science, Faculty of Natural Resources Agriculture and Veterinary Science, The University of Queensland, Brisbane 4072, Australia.

出版信息

Equine Vet J. 2004 Apr;36(3):261-6. doi: 10.2746/0425164044877170.

Abstract

REASONS FOR PERFORMING STUDY

Acute laminitis is characterised by hoof lamellar dermal-epidermal separation at the basement membrane (BM) zone. Hoof lamellar explants cultured in vitro can also be made to separate at the basement membrane zone and investigating how this occurs may give insight into the poorly understood pathophysiology of laminitis.

OBJECTIVES

To investigate why glucose deprivation and metalloproteinase (MMP) activation in cultured lamellar explants leads to dermo-epidermal separation.

METHODS

Explants, cultured without glucose or with the MMP activator p-amino-phenol-mercuric acetate (APMA), were subjected to tension and processed for transmission electron microscopy (TEM).

RESULTS

Without glucose, or with APMA, explants under tension separated at the dermo-epidermal junction. This in vitro separation occurred via 2 different ultrastructural processes. Lack of glucose reduced hemidesmosomes (HDs) numbers until they disappeared and the basal cell cytoskeleton collapsed. Anchoring filaments (AFs), connecting the basal cell plasmalemma to the BM, were unaffected although they failed under tension. APMA activation of constituent lamellar MMPs did not affect HDs but caused AFs to disappear, also leading to dermo-epidermal separation under tension.

CONCLUSIONS

Natural laminitis may occur in situations where glucose uptake by lamellar basal cells is compromised (e.g. equine Cushing's disease, obesity, hyperlipaemia, ischaemia and septicaemia) or when lamellar MMPs are activated (alimentary carbohydrate overload).

POTENTIAL RELEVANCE

Therapies designed to facilitate peripheral glucose uptake and inhibit lamellar MMP activation may prevent or ameliorate laminitis.

摘要

开展本研究的原因

急性蹄叶炎的特征是蹄叶真皮 - 表皮在基底膜(BM)区分离。体外培养的蹄叶外植体也可在基底膜区发生分离,研究其发生机制可能有助于深入了解目前尚不清楚的蹄叶炎病理生理学。

目的

研究体外培养的蹄叶外植体中葡萄糖剥夺和金属蛋白酶(MMP)激活为何会导致真皮 - 表皮分离。

方法

将未添加葡萄糖或添加MMP激活剂对氨基苯酚汞乙酸盐(APMA)培养的外植体施加张力,并进行透射电子显微镜(TEM)处理。

结果

在无葡萄糖或有APMA的情况下,受张力作用的外植体在真皮 - 表皮交界处分离。这种体外分离通过两种不同的超微结构过程发生。缺乏葡萄糖会减少半桥粒(HDs)数量直至其消失,基底细胞细胞骨架塌陷。连接基底细胞质膜与基底膜的锚定丝(AFs)虽不受影响,但在张力作用下断裂。组成蹄叶的MMPs经APMA激活并不影响HDs,但会导致AFs消失,同样在张力作用下导致真皮 - 表皮分离。

结论

天然蹄叶炎可能发生在蹄叶基底细胞葡萄糖摄取受损的情况下(如马库兴氏病、肥胖、高脂血症、缺血和败血症),或蹄叶MMPs被激活时(营养性碳水化合物超载)。

潜在意义

旨在促进外周葡萄糖摄取并抑制蹄叶MMP激活的疗法可能预防或改善蹄叶炎。

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