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通过放射免疫测定法定量牛视网膜和肿瘤提取物中的血管生成因子。

Quantitation of angiogenesis factor in bovine retina and tumour extracts by means of radioimmunoassay.

作者信息

Shahabuddin S, Kumar S

出版信息

Br J Ophthalmol. 1983 May;67(5):286-91. doi: 10.1136/bjo.67.5.286.

Abstract

Using an antiserum raised against tumour angiogenesis factor (TAF) we have developed a radioimmunoassay for retina and tumour angiogenesis factor(s). This antiserum was previously shown to bind to both human and animal tumour extracts and to inhibit the angiogenesis induced by TAF in vivo. TAF from rat Walker tumour was used for iodination by the chloramine-T method. An excess of 125I-labelled TAF was incubated with TAF antibody in the absence (maximum binding) and presence (inhibition of maximum binding) of unlabelled tissue extract. A double antibody technique was used to separate free and bound TAF. Unlabelled human Wilms tumour TAF was used as a standard. The extent of inhibition of 125I-TAF-anti-TAF binding provided a measure of TAF in tissue extracts examined. Extracts of normal bovine retina, cornea, lung, aorta, lymph nodes, iris, vitreous humour, and human tumours and normal human pituitary and liver were assayed. Only bovine retina and human tumours were found to contain angiogenesis factor. These findings, together with our earlier results, suggest that angiogenesis factor from both bovine retina and human tumours induce angiogenesis in vivo and possess common antigenic determinants. The presence of angiogenesis factor in healthy retina and its relationship to neovascularisation in clinical conditions is discussed.

摘要

我们使用针对肿瘤血管生成因子(TAF)产生的抗血清,开发了一种用于视网膜和肿瘤血管生成因子的放射免疫测定法。先前已证明这种抗血清能与人和动物肿瘤提取物结合,并能在体内抑制TAF诱导的血管生成。用氯胺 - T法将来自大鼠Walker肿瘤的TAF进行碘化。在不存在(最大结合)和存在(抑制最大结合)未标记组织提取物的情况下,将过量的125I标记的TAF与TAF抗体一起孵育。采用双抗体技术分离游离的和结合的TAF。未标记的人Wilms肿瘤TAF用作标准品。125I - TAF - 抗TAF结合的抑制程度提供了所检测组织提取物中TAF含量的一种度量。对正常牛视网膜、角膜、肺、主动脉、淋巴结、虹膜、玻璃体液以及人肿瘤和正常人体垂体及肝脏的提取物进行了检测。仅发现牛视网膜和人肿瘤中含有血管生成因子。这些发现与我们早期的结果一起表明,来自牛视网膜和人肿瘤的血管生成因子在体内诱导血管生成并具有共同的抗原决定簇。本文讨论了健康视网膜中血管生成因子的存在及其与临床疾病中新血管形成的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2e/1040044/83af6d115096/brjopthal00161-0015-a.jpg

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