GABAergic interneuron lineages selectively sort into specific cortical layers during early postnatal development.

It is of considerable interest to determine how diverse subtypes of γ-aminobutyric acidergic (GABAergic) interneurons integrate into the functional network of the cerebral cortex. Using inducible in vivo genetic fate mapping approaches, we found that interneuron precursors arising from the medial ganglionic eminence (MGE) and caudal ganglionic eminence (CGE) at E12.5, respectively, populate deep and superficial cortical layers in a complementary manner in the mature cortex. These age-matched populations initiate tangential migration into the cortex simultaneously, migrate above and below the cortical plate in a similar ratio, and complete their entrance into the cortical plate by P1. Surprisingly, while these 2 interneuron populations show a comparable layer distribution at P1, they subsequently segregate into distinct cortical layers. In addition, the initiation of the radial sorting within each lineage coincided well with the upregulation of the potassium/chloride cotransporter KCC2. Moreover, layer sorting of a later born (E16.5) CGE-derived population occurred with a similar time course to the earlier born E12.5 cohorts, further suggesting that this segregation step is controlled in a subtype specific manner. We conclude that radial sorting within the early postnatal cortex is a key mechanism by which the layer-specific integration of GABAergic interneurons into the emerging cortical network is achieved.

[1]  G. Miyoshi,et al.  Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons , 2010, The Journal of Neuroscience.

[2]  E. Anton,et al.  Netrin-1–α3β1 integrin interactions regulate the migration of interneurons through the cortical marginal zone , 2009, Proceedings of the National Academy of Sciences.

[3]  Dante S. Bortone,et al.  KCC2 Expression Promotes the Termination of Cortical Interneuron Migration in a Voltage-Sensitive Calcium-Dependent Manner , 2009, Neuron.

[4]  G. Miyoshi,et al.  Cerebral Cortex doi:10.1093/cercor/bhp038 Characterization of Nkx6-2-Derived , 2009 .

[5]  P. Somogyi,et al.  Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations , 2008, Science.

[6]  S. Anderson,et al.  Fate mapping Nkx2.1‐lineage cells in the mouse telencephalon , 2008, The Journal of comparative neurology.

[7]  O. Marín,et al.  Delineation of Multiple Subpallial Progenitor Domains by the Combinatorial Expression of Transcriptional Codes , 2007, The Journal of Neuroscience.

[8]  H. T. Ghashghaei,et al.  Radial Glial Dependent and Independent Dynamics of Interneuronal Migration in the Developing Cerebral Cortex , 2007, PloS one.

[9]  Arturo Alvarez-Buylla,et al.  Mosaic Organization of Neural Stem Cells in the Adult Brain , 2007, Science.

[10]  G. Miyoshi,et al.  Physiologically Distinct Temporal Cohorts of Cortical Interneurons Arise from Telencephalic Olig2-Expressing Precursors , 2007, The Journal of Neuroscience.

[11]  K. Nakajima Control of tangential/non-radial migration of neurons in the developing cerebral cortex , 2007, Neurochemistry International.

[12]  M. Ekker,et al.  Distinct cis-Regulatory Elements from the Dlx1/Dlx2 Locus Mark Different Progenitor Cell Populations in the Ganglionic Eminences and Different Subtypes of Adult Cortical Interneurons , 2007, The Journal of Neuroscience.

[13]  G. Miyoshi,et al.  Directing neuron-specific transgene expression in the mouse CNS , 2006, Current Opinion in Neurobiology.

[14]  O. Marín,et al.  Layer Acquisition by Cortical GABAergic Interneurons Is Independent of Reelin Signaling , 2006, The Journal of Neuroscience.

[15]  P. Rakic,et al.  Translocation of Synaptically Connected Interneurons across the Dentate Gyrus of the Early Postnatal Rat Hippocampus , 2006, The Journal of Neuroscience.

[16]  Pierre Gressens,et al.  Pathogenesis of migration disorders , 2006, Current opinion in neurology.

[17]  G. Fishell,et al.  The Temporal and Spatial Origins of Cortical Interneurons Predict Their Physiological Subtype , 2005, Neuron.

[18]  M. Calcagnotto,et al.  Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy , 2005, Nature Neuroscience.

[19]  C. Englund,et al.  Postnatal shifts of interneuron position in the neocortex of normal and reeler mice: evidence for inward radial migration , 2004, Neuroscience.

[20]  H. Markram,et al.  Interneurons of the neocortical inhibitory system , 2004, Nature Reviews Neuroscience.

[21]  Arnold R Kriegstein,et al.  Patterns of neuronal migration in the embryonic cortex , 2004, Trends in Neurosciences.

[22]  S. Anderson,et al.  Origins of Cortical Interneuron Subtypes , 2004, The Journal of Neuroscience.

[23]  C. Branda,et al.  Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice. , 2004, Developmental cell.

[24]  T. Kaneko,et al.  Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67‐GFP knock‐in mouse , 2003, The Journal of comparative neurology.

[25]  O. Marín,et al.  Cell migration in the forebrain. , 2003, Annual review of neuroscience.

[26]  Y. Morozov,et al.  Post‐natal development of type 1 cannabinoid receptor immunoreactivity in the rat hippocampus , 2003, The European journal of neuroscience.

[27]  P. Rakic,et al.  Four-Dimensional Migratory Coordinates of GABAergic Interneurons in the Developing Mouse Cortex , 2003, The Journal of Neuroscience.

[28]  Seong-Seng Tan,et al.  Layer Specification of Transplanted Interneurons in Developing Mouse Neocortex , 2003, The Journal of Neuroscience.

[29]  D. O'Leary,et al.  Dynamic Patterned Expression of Orphan Nuclear Receptor Genes RORα and RORβ in Developing Mouse Forebrain , 2003, Developmental Neuroscience.

[30]  D. O'Leary,et al.  Dynamic patterned expression of orphan nuclear receptor genes RORalpha and RORbeta in developing mouse forebrain. , 2003, Developmental neuroscience.

[31]  G. Fishell,et al.  The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations , 2002, Nature Neuroscience.

[32]  W. Dobyns,et al.  Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans , 2002, Nature Genetics.

[33]  Arnold R. Kriegstein,et al.  Is there more to gaba than synaptic inhibition? , 2002, Nature Reviews Neuroscience.

[34]  G. Fishell,et al.  Telencephalic cells take a tangent: non-radial migration in the mammalian forebrain , 2001, Nature Neuroscience.

[35]  Chris J. McBain,et al.  Interneurons unbound , 2001, Nature Reviews Neuroscience.

[36]  J. A. Payne,et al.  The K+/Cl− co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation , 1999, Nature.

[37]  C. Houser,et al.  Evidence for changing positions of GABA neurons in the developing rat dentate gyrus , 1999, Hippocampus.

[38]  David J. Anderson,et al.  Fate mapping of the mouse midbrain–hindbrain constriction using a site-specific recombination system , 1998, Current Biology.

[39]  Y. Kubota,et al.  GABAergic cell subtypes and their synaptic connections in rat frontal cortex. , 1997, Cerebral cortex.

[40]  Y. Ben-Ari,et al.  Giant synaptic potentials in immature rat CA3 hippocampal neurones. , 1989, The Journal of physiology.

[41]  A. Fairén,et al.  Times of generation of glutamic acid decarboxylase immunoreactive neurons in mouse somatosensory cortex , 1986, The Journal of comparative neurology.

[42]  M. Miller,et al.  Cogeneration of retrogradely labeled corticocortical projection and GABA-immunoreactive local circuit neurons in cerebral cortex. , 1985, Brain research.

[43]  P. Rakić Neurons in Rhesus Monkey Visual Cortex: Systematic Relation between Time of Origin and Eventual Disposition , 1974, Science.

[44]  R. Sidman,et al.  Autoradiographic Study of Cell Migration during Histogenesis of Cerebral Cortex in the Mouse , 1961, Nature.

[45]  J. Hirschfeld,et al.  Distribution of Group-specific Components (Gc) in the Sera of Native Africans , 1961, Nature.