Abstract
The ability of stem cells to self-renew has hung been attributed to an asymmetry in division that generates one daughter cell identical to the mother and another cell committed to differentiation. Recent studies on neuroblasts, a group of neural stem cells responsible for generating various neurons and glial cells in the central nervous system, have revealed exciting mechanisms that underlie self-renewing asymmetric division. Several important localized cell fate determinants have been characterized, and their segregation mechanism has been explored in the context of cytoskeletal organization, cell-cycle type progression, cytokinesis and mitotic orientation. These findings are illuminating in understanding the general mechanism of stem cell division.
Publication types
-
Research Support, Non-U.S. Gov't
-
Research Support, U.S. Gov't, P.H.S.
-
Review
MeSH terms
-
Animals
-
Cell Differentiation
-
Cell Division
-
Drosophila / embryology
-
Drosophila / physiology
-
Drosophila Proteins*
-
Gene Expression Regulation, Developmental
-
Juvenile Hormones / physiology
-
Mammals / physiology
-
Membrane Proteins / physiology
-
Models, Biological
-
Nerve Tissue Proteins / physiology
-
Neurons / cytology*
-
Neurons / physiology*
-
Nuclear Proteins / physiology
-
Receptors, Notch
-
Signal Transduction
-
Stem Cells / cytology
-
Stem Cells / physiology*
-
Transcription Factors*
Substances
-
Drosophila Proteins
-
Juvenile Hormones
-
Membrane Proteins
-
N protein, Drosophila
-
Nerve Tissue Proteins
-
Nuclear Proteins
-
Receptors, Notch
-
Transcription Factors
-
numb protein, Drosophila
-
pros protein, Drosophila