Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Shlomo Dellal
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Manuel Valero
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Hector Zurita
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Ilya Kruglikov
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
John Hongyu Meng
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States; Center for Neural Science, New York University, New York, United States
Jessica L Hanson
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Yoshiko Hashikawa
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Benjamin Schuman
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States; Department of Neuroscience and Physiology, New York University Grossman School of Medicine, New York, United States
Neuroscience Institute, New York University Grossman School of Medicine, New York, United States; Department of Neuroscience and Physiology, New York University Grossman School of Medicine, New York, United States; Department of Anesthesiology, Perioperative Care and Pain Medicine, New York University Grossman School of Medicine, New York, United States
Cortical GABAergic interneurons (INs) represent a diverse population of mainly locally projecting cells that provide specialized forms of inhibition to pyramidal neurons and other INs. Most recent work on INs has focused on subtypes distinguished by expression of Parvalbumin (PV), Somatostatin (SST), or Vasoactive Intestinal Peptide (VIP). However, a fourth group that includes neurogliaform cells (NGFCs) has been less well characterized due to a lack of genetic tools. Here, we show that these INs can be accessed experimentally using intersectional genetics with the gene Id2. We find that outside of layer 1 (L1), the majority of Id2 INs are NGFCs that express high levels of neuropeptide Y (NPY) and exhibit a late-spiking firing pattern, with extensive local connectivity. While much sparser, non-NGFC Id2 INs had more variable properties, with most cells corresponding to a diverse group of INs that strongly expresses the neuropeptide CCK. In vivo, using silicon probe recordings, we observed several distinguishing aspects of NGFC activity, including a strong rebound in activity immediately following the cortical down state during NREM sleep. Our study provides insights into IN diversity and NGFC distribution and properties, and outlines an intersectional genetics approach for further study of this underappreciated group of INs.