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Related Concept Videos

Differentiation of Common Myeloid Progenitor Cells01:15

Differentiation of Common Myeloid Progenitor Cells

Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...
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Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...

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Related Experiment Video

Updated: Jul 13, 2026

Patient Derived Cell Culture and Isolation of CD133+ Putative Cancer Stem Cells from Melanoma
12:16

Patient Derived Cell Culture and Isolation of CD133+ Putative Cancer Stem Cells from Melanoma

Published on: March 13, 2013

CD133 (AC133) expression on AML cells and progenitors.

S M Vercauteren1, H J Sutherland

  • 1Terry Fox Laboratory, British Columbia Cancer Agency Vancouver Hospital and Health Sciences Centre, Vancouver, BC Canada.

Cytotherapy
|April 16, 2002
PubMed
Summary

CD133 expression does not predict outcomes in acute myeloid leukemia (AML). While CD133 marks primitive leukemic progenitors in vitro, it cannot be used to isolate them in vivo.

Area of Science:

  • Hematology
  • Cancer Biology
  • Cellular Hierarchy

Background:

  • Acute myeloid leukemia (AML) exhibits a hierarchy of progenitor cells with varying functional capabilities.
  • CD133 (AC133) is a transmembrane protein found on normal hematopoietic progenitors (CD34(+) and CD34(-)).
  • This study investigates the prognostic value of CD133 expression in AML and its presence on disease-maintaining AML progenitors.

Purpose of the Study:

  • To determine the prognostic significance of CD133 expression in acute myeloid leukemia (AML).
  • To characterize the expression of CD133 on AML progenitors responsible for disease maintenance.
  • To assess the utility of CD133 for purifying primitive leukemic progenitors.

Main Methods:

  • Analysis of CD133 and CD34 expression in AML cells from 102 patients.

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  • Correlation of CD133/CD34 expression with clinical outcomes in 92 treated AML patients.
  • Flow cytometry sorting of AML cells into CD34/CD133 subfractions for in vitro (CFU, SC) and in vivo (NOD/SCID mice) assays.
  • Main Results:

    • CD133 expression did not correlate with survival, FAB subtype, cytogenetics, or white blood cell count (WBCC) in AML.
    • CD133 expression was correlated with CD34 expression.
    • Leukemic progenitors capable of forming colonies (CFU) and engrafting immunodeficient mice (NOD/SCID) were found across all CD34/CD133 subfractions, including CD34(-)/CD133(-).

    Conclusions:

    • CD133 is not a reliable prognostic marker for AML.
    • CD133 is co-expressed with CD34 on primitive leukemic progenitors detected in vitro.
    • CD133 alone cannot be used to purify in vivo leukemic progenitors in AML patients.