TY - JOUR
T1 - Mechanisms of neural stem cell fate determination
T2 - extracellular cues and intracellular programs.
AU - Abematsu, Masahiko
AU - Smith, Ian
AU - Nakashima, Kinichi
PY - 2006/1/1
Y1 - 2006/1/1
N2 - Multipotent neural stem cells (NSC) possess the ability to self-renew and to generate the three major central nervous system (CNS) cell types: neurons, astrocytes and oligodendrocytes. However, the molecular mechanisms that control NSC fate specification are not yet fully understood. Recent studies have provided evidence that soluble protein mediators such as cytokines and transcriptional factors play critical roles in cell fate determination. Furthermore, it has become apparent that epigenetic gene regulation plays an important intracellular role as cell-intrinsic programs in the specification of cell lineages. In this review, we focus on recent progress that addresses the mechanisms of NSC fate specification and their possible contribution in the field of regenerative medicine.
AB - Multipotent neural stem cells (NSC) possess the ability to self-renew and to generate the three major central nervous system (CNS) cell types: neurons, astrocytes and oligodendrocytes. However, the molecular mechanisms that control NSC fate specification are not yet fully understood. Recent studies have provided evidence that soluble protein mediators such as cytokines and transcriptional factors play critical roles in cell fate determination. Furthermore, it has become apparent that epigenetic gene regulation plays an important intracellular role as cell-intrinsic programs in the specification of cell lineages. In this review, we focus on recent progress that addresses the mechanisms of NSC fate specification and their possible contribution in the field of regenerative medicine.
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U2 - 10.2174/157488806776956887
DO - 10.2174/157488806776956887
M3 - Review article
C2 - 18220872
AN - SCOPUS:33749467484
SN - 1574-888X
VL - 1
SP - 267
EP - 277
JO - Current stem cell research & therapy
JF - Current stem cell research & therapy
IS - 2
ER -