Related Experiment Video
Updated: May 19, 2026

14:08
Blastomere Explants to Test for Cell Fate Commitment During Embryonic Development
Published on: January 26, 2013
FoxOs in neural stem cell fate decision.
Seung-Hyun Ro1, Debra Liu, Hyeonju Yeo
1Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
Archives of Biochemistry and Biophysics
|August 21, 2012
Summary
Neural stem cells (NSCs) maintain brain homeostasis through self-renewal and quiescence. The PI3K-Akt-FoxO pathway, particularly FoxO transcription factors, is crucial for regulating NSC fate and function.
Area of Science:
- Neuroscience
- Stem Cell Biology
- Molecular Biology
Background:
- Neural stem cells (NSCs) are vital for lifelong brain maintenance, requiring self-renewal and quiescence.
- Aberrant proliferation or differentiation of NSCs can lead to malignant growth or premature depletion.
- The PI3K-Akt-FoxO signaling pathway is implicated in regulating various stem cell types, including brain NSCs.
Purpose of the Study:
- To review the current understanding of FoxO transcription factor function in neural stem cells.
- To discuss the biological activities of FoxO factors that influence neural stem cell fate.
Main Methods:
- Literature review focusing on the PI3K-Akt-FoxO pathway and FoxO transcription factors in NSCs.
- Analysis of existing research on stem cell regulation, proliferation, differentiation, and homeostasis.
Main Results:
- FoxO transcription factors are highly expressed in mammalian brain NSCs.
- FoxO factors act as key downstream effectors regulating NSC proliferation, oxidative stress response, and homeostasis.
- These factors are critical for maintaining the long-term repopulating potential of NSCs.
Conclusions:
- FoxO transcription factors play a central role in determining neural stem cell fate.
- Understanding FoxO function is essential for comprehending neural stem cell maintenance and brain homeostasis.
More Related Videos
Related Concept Videos
Lineage Commitment
Commitment is the process whereby stem cells:
Stem Cell Niche
The stem cell niche is the dynamic microenvironment where stem cells reside. Inside these niches, the cells may remain undifferentiated, undergo high self-renewal, or become lineage-specific progenitors. Stem cells coexist with other niche cells, such as stromal cells. They also interact closely with the ECM. Cell-cell and cell-matrix communication occur via adhesion molecules or soluble factors that signal the stem cells and determine their fate. Stromal cells also provide survival signals to...
Embryonic Stem Cells
Embryonic stem (ES) cells are undifferentiated pluripotent cells, meaning they can produce any cell type in the body. This gives them tremendous potential in science and medicine since they can generate specific cell types for use in research or to replace body cells lost due to damage or disease.
Embryonic Stem Cells
Embryonic stem (ES) cells were first discovered in mice in 1981 by Martin Evans. In 1998, James Thomson identified a method to isolate embryonic stem cells from humans. Human embryonic stem cells (hESCs) are obtained from 3-5 day old embryos that remain unused after an in vitro fertilization procedure.
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
Zygotic Development And Stem Cell Formation
The development of all multicellular organisms starts with the fusion of haploid cells called sperm and egg to form a diploid zygote. A zygote is a totipotent cell that can develop into a complete organism. The zygote undergoes cell division or cleavage to form an 8-cell mass. Until this stage, the cells are spherical, loosely attached, and remain totipotent. Totipotent cells are capable of developing both the embryonic and the extraembryonic tissues. However, as they continue to divide, they...
Determination
During embryogenesis, cells become progressively committed to different fates through a two-step process: specification followed by determination. Specification is demonstrated by removing a segment of an early embryo, “neutrally” culturing the tissue in vitro—for example, in a petri dish with simple medium—and then observing the derivatives. If the cultured region gives rise to cell types that it would normally generate in the embryo, this means that it is specified. In contrast, determination...

