Author
Listed:
- Chungkil Won
(Harvard Medical School
Angiogenesis and Brain Development Laboratory, McLean Hospital)
- Zhicheng Lin
(Harvard Medical School
McLean Hospital)
- Peeyush Kumar T.
(Harvard Medical School
Angiogenesis and Brain Development Laboratory, McLean Hospital)
- Suyan Li
(Harvard Medical School
Angiogenesis and Brain Development Laboratory, McLean Hospital)
- Lai Ding
(Enhanced Neuroimaging Core, Harvard NeuroDiscovery Center, Harvard Medical School)
- Abdallah Elkhal
(Harvard Medical School
Brigham and Women’s Hospital)
- Gábor Szabó
(Laboratory of Molecular Biology and Genetics, Institute of Experimental Medicine)
- Anju Vasudevan
(Harvard Medical School
Angiogenesis and Brain Development Laboratory, McLean Hospital)
Abstract
Gamma-aminobutyric acid neurons, born in remote germinative zones in the ventral forebrain (telencephalon), migrate tangentially in two spatially distinct streams to adopt their specific positions in the developing cortex. The cell types and molecular cues that regulate this divided migratory route remains to be elucidated. Here we show that embryonic vascular networks are strategically positioned to fulfil the task of providing support as well as critical guidance cues that regulate the divided migratory routes of gamma-aminobutyric acid neurons in the telencephalon. Interestingly, endothelial cells of the telencephalon are not homogeneous in their gene expression profiles. Endothelial cells of the periventricular vascular network have molecular identities distinct from those of the pial network. Our data suggest that periventricular endothelial cells have intrinsic programs that can significantly mould neuronal development and uncovers new insights into concepts and mechanisms of central nervous system angiogenesis from both developmental and disease perspectives.
Suggested Citation
Chungkil Won & Zhicheng Lin & Peeyush Kumar T. & Suyan Li & Lai Ding & Abdallah Elkhal & Gábor Szabó & Anju Vasudevan, 2013.
"Autonomous vascular networks synchronize GABA neuron migration in the embryonic forebrain,"
Nature Communications, Nature, vol. 4(1), pages 1-14, October.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3149
DOI: 10.1038/ncomms3149
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