4.4 Article

MACF1 regulates the migration of pyramidal neurons via microtubule dynamics and GSK-3 signaling

期刊

DEVELOPMENTAL BIOLOGY
卷 395, 期 1, 页码 4-18

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2014.09.009

关键词

MACF1; Neuronal migration; Cytoskeleton; Microtubule; GSK-3

资金

  1. Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health [P20GM103471]
  2. NE DHHS [2012-05]
  3. Alzheimer's Association [NIRP-12-258440]

向作者/读者索取更多资源

Neuronal migration and subsequent differentiation play critical roles for establishing functional neural circuitry in the developing brain. However, the molecular mechanisms that regulate these processes are poorly understood. Here, we show that microtubule actin crosslinking factor 1 (MACF1) determines neuronal positioning by regulating microtubule dynamics and mediating GSK-3 signaling during brain development. First, using MACF1 foxed allele mice and in utero gene manipulation, we find that MACF1 deletion suppresses migration of cortical pyramidal neurons and results in aberrant neuronal positioning in the developing brain. The cell autonomous deficit in migration is associated with abnormal dynamics of leading processes and centrosomes. Furthermore, microtubule stability is severely damaged in neurons lacking MACF1, resulting in abnormal microtubule dynamics. Finally, MACF1 interacts with and mediates GSK-3 signaling in developing neurons. Our findings establish a cellular mechanism underlying neuronal migration and provide insights into the regulation of cytoskeleton dynamics in developing neurons. (C) 2014 Elsevier Inc. All rights reserved.

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