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小鼠主动脉环实验:血管生成分子遗传学的新方法。

Mouse Aortic Ring Assay: A New Approach of the Molecular Genetics of Angiogenesis.

作者信息

Masson V V éRonique, Devy Laetitia, Grignet-Debrus Christine, Bernt Sarah, Bajou Khalid, Blacher Silvia, Roland Guy, Chang Yawen, Fong Timothy, Carmeliet Peter, Foidart Jean-Michel, Noël Agnès

机构信息

Laboratory of Tumor and Developmental Biology, Université de Liège. Tour de Pathologie (B23), Sart Tilman, B-4000 Liège. Belgium.; Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Katholieke Universiteit Leuven. B-3000 Leuven. Belgium.Rhone-Poulenc Rorer. Hayward, California, 94545. USA.

出版信息

Biol Proced Online. 2002 Oct 28;4:24-31. doi: 10.1251/bpo30.

Abstract

Angiogenesis, a key step in many physiological and pathological processes, involves proteolysis of the extracellular matrix. To study the role of two enzymatic families, serine-proteases and matrix metalloproteases in angiogenesis, we have adapted to the mouse, the aortic ring assay initially developed in the rat. The use of deficient mice allowed us to demonstrate that PAI-1 is essential for angiogenesis while the absence of an MMP, MMP-11, did not affect vessel sprouting. We report here that this model is attractive to elucidate the cellular and molecular mechanisms of angiogenesis, to identify, characterise or screen "pro- or anti-angiogenic agents that could be used for the treatment of angiogenesis-dependent diseases. Approaches include using recombinant proteins, synthetic molecules and adenovirus-mediated gene transfer.

摘要

血管生成是许多生理和病理过程中的关键步骤,涉及细胞外基质的蛋白水解。为了研究丝氨酸蛋白酶和基质金属蛋白酶这两个酶家族在血管生成中的作用,我们将最初在大鼠中开发的主动脉环试验应用于小鼠。使用基因缺陷小鼠使我们能够证明纤溶酶原激活物抑制剂-1(PAI-1)对血管生成至关重要,而基质金属蛋白酶-11(MMP-11)的缺失并不影响血管芽生。我们在此报告,该模型对于阐明血管生成的细胞和分子机制、鉴定、表征或筛选可用于治疗血管生成依赖性疾病的“促血管生成或抗血管生成剂”具有吸引力。方法包括使用重组蛋白、合成分子和腺病毒介导的基因转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0897/145553/0d0a06b908f7/m30f1lg.jpg

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