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Related Concept Videos

Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...
Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

Role Of Notch Signalling In Intestinal Stem Cell Renewal

Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Adult Stem Cells01:33

Adult Stem Cells

Stem cells are undifferentiated cells that divide and produce more stem cells or progenitor cells that differentiate into mature, specialized cell types. All the cells in the body are generated from stem cells in the early embryo, but small populations of stem cells are also present in many adult tissues including the bone marrow, brain, skin, and gut. These adult stem cells typically produce the various cell types found in that tissue—to replace cells that are damaged or to continuously renew...

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A Three-dimensional Model of Spheroids to Study Colon Cancer Stem Cells
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CD133+ CD44+ subgroups may be human small intestinal stem cells.

Neng-Yi Hou1, Kun Yang, Tie Chen

  • 1Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, No. 37 Guo Xue Xiang, Chengdu, 610041, Sichuan Province, People's Republic of China.

Molecular Biology Reports
|June 8, 2010
PubMed
Summary
This summary is machine-generated.

Researchers identified CD133(+)CD44(+) cells as potential human small intestinal epithelial stem cells. This finding aids in the preliminary identification and separation of these crucial cells for further study.

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Area of Science:

  • Gastroenterology
  • Stem Cell Biology
  • Cellular and Molecular Medicine

Background:

  • Identifying and isolating small intestinal epithelial stem cells is challenging.
  • Current methods for stem cell identification are preliminary.

Purpose of the Study:

  • To investigate CD133 and CD44 as potential markers for human small intestinal epithelial stem cells.
  • To explore the expression of Lgr5 in relation to CD133 and CD44 markers.

Main Methods:

  • Immunohistochemistry was used to study the expression of CD133, CD44, and Lgr5.
  • Fluorescence-activated cell sorting (FACS) was employed to isolate cell subgroups based on CD133 and CD44 expression.
  • RT-PCR and PAGE with silver staining were utilized to measure Lgr5 gene expression levels.

Main Results:

  • Immunohistochemistry showed overlapping expression of CD133, CD44, and Lgr5 in cells at the bottom of crypts.
  • FACS analysis identified distinct percentages for CD133(+)CD44(+), CD133(+)CD44(-), CD133(-)CD44(+), and CD133(-)CD44(-) cell populations.
  • Lgr5 gene expression was significantly higher in the CD133(+)CD44(+) subgroup compared to other subgroups (P < 0.001).

Conclusions:

  • CD133(+)CD44(+) cells show promise as human small intestinal epithelial stem cells.
  • Further research is required to confirm the definitive role of these cells.
  • This study provides a foundation for improved stem cell isolation techniques.