Endothelial Cell Viability

Endothelial cell viability is the capacity of endothelial cells to remain alive, metabolically active, and functionally intact under defined conditions. It is commonly evaluated by measuring membrane integrity, metabolic activity, and responses to stress, because cell death or dysfunction can compromise barrier formation and vascular signaling. In bioengineering, viability assessment helps optimize culture conditions, biomaterials, microfluidic vessels, and tissue-engineered vascular grafts; viable endothelial layers can support selective permeability, reduce the thrombogenicity of surfaces, and improve the physiological relevance of engineered vascular models.

Endothelial Cell Viability - Related Videos

Research

JoVE Journal - Biology

Viability Assays for Cells in Culture

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Cited by 35 •

2014

Therapeutic compounds are often first examined in vitro with viability assays. Blind cell counts by a human observer can be highly sensitive to small changes in cell number but do not assess function. Computerized viability assays, as described here, can assess both structure and function in an objective manner.

Counting and Determining the Viability of Cultured Cells

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Cited by 19 •

2008

Determining the number of cells in culture is important in standardization of culture conditions and in performing accurate quantitation experiments. In this video, we demonstrate how cells are counted using a hemacytometer.

Research

JoVE Journal - Biology

Isolation of Mouse Pancreatic Endothelial Cells

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2024

This protocol describes the isolation of mouse endothelial cells from whole pancreas.

Isolation of Murine Retinal Endothelial Cells for Next-Generation Sequencing

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Cited by 4 •

2021

This protocol describes a method for the isolation of murine postnatal retinal endothelial cells optimized for cell yield, purity, and viability. These cells are suitable for next-generation sequencing approaches.

Research

JoVE Journal - Developmental Biology
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Isolation of Murine Embryonic Hemogenic Endothelial Cells

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Cited by 10 •

2016

Hematopoietic stem and progenitor cells (HSPC) derive from specialized (hemogenic) endothelial cells during development, yet little is known about the process by which some endothelial cells specify to become blood forming. We demonstrate a flow-cytometry based method allowing simultaneous isolation of hemogenic endothelial cells and HSPC from murine embryonic tissues.

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