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Imaging Blood Vessels and Lymphatics in Mouse Trachea Wholemounts.

Methods in molecular biology (Clifton, N.J.) (2022-02-01)
Peter Baluk, Donald M McDonald
要旨

Changes in blood vessels and lymphatics in health and disease are easier to understand and interpret when studied microscopically in three dimensions. The mouse trachea is a simple, yet powerful, and versatile model system in which to achieve this. We describe practical immunohistochemical methods for fluorescence and confocal microscopy of wholemounts of the mouse trachea to achieve this purpose in which the entire vasculature can be visualized from the organ level to the cellular and subcellular level. Blood vessels and lymphatics have highly stereotyped vascular architectures that repeat in arcades between the tracheal cartilages. Arterioles, capillaries, and venules can be easily identified for the blood vessels, while the lymphatics consist of initial lymphatics and collecting lymphatics. Even small abnormalities in either blood vessels or lymphatics can be noticed and evaluated in three dimensions. We and others have used the mouse trachea for examining in situ angiogenesis and lymphangiogenesis, vascular development and regression, vessel patency, differences in transgenic mice, and pathological changes, such as increased vascular permeability induced by inflammatory mediators.

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Sigma-Aldrich
抗アセチル化チューブリン抗体、マウスモノクローナル マウス宿主抗体, clone 6-11B-1, purified from hybridoma cell culture
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抗アクチンα-平滑筋-FITC抗体、マウスモノクローナル マウス宿主抗体, clone 1A4, purified from hybridoma cell culture
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抗ホスホヒストンH3 (Ser10)抗体、有糸分裂マーカー, Upstate®, from rabbit
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抗NG2コンドロイチン硫酸プロテオグリカン抗体, Chemicon®, from rabbit
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抗クララ細胞分泌タンパク質抗体, serum, Upstate®
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Anti-VCAM-1 (CD106) Antibody, clone 6C7.1, clone 6C7.1, from rat