Intestinal Stem Cell Isolation

Intestinal stem cell isolation is a biological method for separating self-renewing stem cells from intestinal tissue so their maintenance, differentiation, and regenerative capacity can be studied in controlled laboratory systems. The process commonly involves collecting intestinal crypts, releasing cells through mechanical and enzymatic dissociation, and enriching or identifying stem cells using features such as LGR5 expression before culture in defined, growth-factor-containing media. Isolated cells can generate intestinal organoids that model epithelial renewal, tissue injury, disease, and responses to candidate therapeutics. This approach supports research in developmental biology, gastrointestinal pathology, and regenerative medicine while enabling analysis of stem cell behavior outside native tissue.

Intestinal Stem Cell Isolation - Related Videos

Research

JoVE Journal - Biology

Isolation and Transplantation of Hematopoietic Stem Cells (HSCs)

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Cited by 31 •

2007

Isolating Stem Cells from Soft Musculoskeletal Tissues

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Cited by 21 •

2010

Isolating adult stem cells from musculoskeletal soft tissues based on the cell's adherence speed to flask.

Research

JoVE Journal - Medicine
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Intestinal Stem Cell Isolation and Culture in a Porcine Model of Segmental Small Intestinal Ischemia

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Cited by 15 •

2018

This protocol will enable readers to successfully establish a porcine model of segmental intestinal ischemia and subsequently isolate and culture intestinal stem cells for the study of epithelial repair following injury.

Intestinal Crypts Isolation: A Method to Isolate Whole Crypts from Small Intestine of Murine Model

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2023

In this video, we demonstrate a technique to isolate whole crypts from a mouse’s small intestine. The isolated whole crypts can be used to propagate long-lived and self-renewing 3D organoids in vitro.

Isolation and Characterization of Dendritic Cells and Macrophages from the Mouse Intestine

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Cited by 68 •

2012

Here, we detail a methodology for the rapid isolation of mouse intestinal dendritic cells (DCs) and macrophages. Phenotypic characterization of intestinal DCs and macrophages is performed using multi-color flow cytometric analysis while magnetic bead enrichment followed by cell sorting is used to yield highly pure populations for functional studies.

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