Protocol for in vivo and in vitro study of lymphatic valve formation driven by shear stress signaling pathway.
Protocol for in vivo and in vitro study of lymphatic valve formation driven by shear stress signaling pathway.
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DOI:
10.1016/j.xpro.2023.102141
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发表时间:
2023-04-17
期刊:
影响因子:
--
通讯作者:
Yang, Ying
中科院分区:
文献类型:
--
作者:
Banerjee, Richa;Knauer, Luz A.;Yang, Ying
Here we detail a protocol for the isolation and processing of lymphatic enriched tissue of mouse models for the purpose of immunostaining and quantification of lymphatic valves, vessel length, and vessel diameter. Furthermore, we describe an optimized protocol for exposing treated human dermal lymphatic endothelial cells to flow for the purpose of studying lymph shear stress responses via gene expression and protein detection methods. This approach is useful to study lymphatic valve formation driven by oscillatory shear stress. For complete details on the use and execution of this protocol, please refer to Scallan et al. (2021). Detailed steps for harvesting lymphatic vessel enriched tissues Morphological analysis of lymphatic vessels and valves using ex vivo imaging Steps for precise quantification of valve number, vessel length, and vessel diameter Steps for investigating flow responses in cultured human lymphatic endothelial cells Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. Here we detail a protocol for the isolation and processing of lymphatic enriched tissue of mice models for the purpose of immunostaining and quantification of lymphatic valves, vessel length, and vessel diameter. Furthermore, we describe an optimized protocol for exposing treated human dermal lymphatic endothelial cells to flow for the purpose of studying lymph shear stress responses via gene expression and protein detection methods. This approach is useful to study lymphatic valve formation driven by oscillatory shear stress.
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