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建立鸡胚卵黄囊膜(YSM)在体分析方法,用于初步筛选潜在的血管生成和抗血管生成药物。

Establishment of an in ovo chick embryo yolk sac membrane (YSM) assay for pilot screening of potential angiogenic and anti-angiogenic agents.

机构信息

School of Regenerative Medicine, Manipal University, Bangalore 560065, Karnataka, India.

Prof. Ramkrishna More Arts, Science and Commerce College, Akurdi, Pune 411044, Maharashtra, India.

出版信息

Cell Biol Int. 2018 Nov;42(11):1474-1483. doi: 10.1002/cbin.11051. Epub 2018 Sep 11.

Abstract

Angiogenesis, the process of new blood vessel formation from pre-existing vessels, is essential for growth and development. Development of drugs that can accelerate or decelerate angiogenesis in the context of various diseases requires appropriate preclinical screening. As angiogenesis involves complex cellular and molecular processes, in vivo studies are superior to in vitro investigations. Conventional in vitro, in vivo, and ex ovo models of angiogenesis are time consuming and tedious, and require sophisticated infrastructure for embryo culture. In the present study, we established an in ovo chick embryo yolk sac membrane (YSM) assay for angiogenesis and tested the angiogenic potential of arginine, conditioned medium (CM) from human adipose tissue and placenta-derived mesenchymal stem cells (ADMSCs-CM and PDMSCs-CM), avastin and vitamin C. The obtained results were confirmed with the routinely employed chick embryo Chorioallantoic Membrane (CAM) assay. Both assays revealed the pro-angiogenic nature of arginine, ADMSCs-CM, and PDMSCs-CM, and the anti-angiogenic effect of avastin and vitamin C. This novel in ovo YSM model is simple, reproducible, and highly economic in terms of the time frame and cost incurred. The proposed model is thus a suitable substitute to the CAM model for pilot screening of potential angiogenic and anti-angiogenic agents.

摘要

血管生成,即从现有血管形成新血管的过程,对于生长和发育至关重要。为了在各种疾病的背景下加速或减缓血管生成,需要开发能够加速或减缓血管生成的药物,这就需要进行适当的临床前筛选。由于血管生成涉及复杂的细胞和分子过程,因此体内研究优于体外研究。传统的血管生成体外、体内和鸡胚外模型既耗时又乏味,并且需要复杂的胚胎培养基础设施。在本研究中,我们建立了一种鸡胚卵黄囊膜(YSM)血管生成检测方法,并测试了精氨酸、人脂肪组织和胎盘间充质干细胞(ADMSCs-CM 和 PDMSCs-CM)条件培养基、阿瓦斯汀和维生素 C 的血管生成潜力。通过常规使用的鸡胚尿囊膜(CAM)检测方法验证了获得的结果。两种检测方法均显示了精氨酸、ADMSCs-CM 和 PDMSCs-CM 的促血管生成特性,以及阿瓦斯汀和维生素 C 的抗血管生成作用。这种新颖的鸡胚 YSM 模型简单、可重复,在时间框架和成本方面具有高度经济性。因此,该模型是 CAM 模型的合适替代品,可用于潜在的血管生成和抗血管生成药物的初步筛选。

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