使用吡咪唑来表征体内组织工程室内环境中的缺氧

S.O.P. Hofer, G.M. Mitchell, A.J. Penington, W.A. Morrison, R. RomeoMeeuw, E. Keramidaris, J. Palmer, K.R. Knight
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引用次数: 48

摘要

缺氧细胞在体内组织工程腔内的分布在植入后28天进行了研究。方法采用基底膜凝胶(BM凝胶)将大鼠成纤维细胞置于含有2×106的双瓣聚碳酸酯腔内。在雄性大鼠腹股沟皮下插入腔室,分别于3 (n=6)、7 (n=6)、14 (n=4)和28 (n=4)天取出。收获前90分钟,腹腔注射吡莫硝唑(60 mg/kg)。取出腔室组织,浸泡固定,石蜡包埋,切片并使用hypoxyprobe-1 Mab进行免疫组织化学染色,该Mab检测细胞中形成的还原吡硝唑加合物,pO2<10 mmHg。结果3天后,纤维蛋白凝块/BM凝胶框架填充腔室。有籽的成纤维细胞大部分死亡。大多数3天的腔室没有显示AV环的组织生长,也没有吡莫硝唑结合在这些腔室中。在组织生长发生的一个腔室中,新组织内明显存在强的吡莫硝唑结合。在6个7天的腔室中,有4个腔室的增生区较宽,从房室环内皮延伸至0.4 mm(约),显示出强烈的吡莫硝唑结合。其余两个7天的腔室显示出更大的组织生长(前沿距房室环内皮0.7 mm),但非常弱或没有吡莫硝唑结合。在第14和28天,纤维蛋白/BM凝胶基质被不结合吡莫硝唑的成熟血管结缔组织所取代。结论采用组织工程腔室,新组织生长至距房室环内皮0.4 mm(腔室≤7天),表现出强烈的吡莫硝唑结合,因此出现缺氧。距离房室环内皮(7-28天的腔室)大于0.5 mm的组织生长由于新血管数量的显著增加而没有表现出吡莫硝唑结合,因此被充分充氧。
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The use of pimonidazole to characterise hypoxia in the internal environment of an in vivo tissue engineering chamber

The distribution of hypoxic cells in an in vivo tissue engineering chamber was investigated up to 28 days post-implantation.

Methods

Arteriovenous loops were constructed and placed into bi-valved polycarbonate chambers containing 2×106 rat fibroblasts in basement membrane gel (BM gel). Chambers were inserted subcutaneously in the groin of male rats and harvested at 3 (n=6), 7 (n=6), 14 (n=4) or 28 (n=4) days. Ninety minutes before harvest, pimonidazole (60 mg/kg) was injected intraperitoneally. Chamber tissue was removed, immersion fixed, paraffin embedded, sectioned and stained immunohistochemically using hypoxyprobe-1 Mab that detects reduced pimonidazole adducts forming in cells, where pO2<10 mmHg.

Results

At 3 days a fibrin clot/BM gel framework filled the chamber. Seeded fibroblasts had largely died. The majority of 3 day chambers did not demonstrate tissue growth from the AV loop nor was pimonidazole binding present in these chambers. In one chamber in which tissue growth had occurred strong pimonidazole binding was evident within the new tissue. In four out of six 7 day chambers a broader proliferative zone existed extending up to 0.4 mm (approximately) from the AV loop endothelium which demonstrated intense pimonidazole binding. The two remaining 7 day chambers displayed even greater tissue growth (leading edge>0.7 mm from the AV loop endothelium), but very weak or no pimonidazole binding. At 14 and 28 days the fibrin/BM gel matrix was replaced by mature vascularised connective tissue that did not bind pimonidazole.

Conclusion

Employing a tissue engineering chamber, new tissue growth extending up to 0.4 mm from the AV loop endothelium (chambers≤7 days) demonstrated intense pimonidazole binding and, therefore, hypoxia. Tissue growth greater than 0.5 mm from the AV loop endothelium (7–28 days chambers) did not exhibit pimonidazole binding due to a significant increase in the number of new blood vessels and was, therefore, adequately oxygenated.

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