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      <comment>Funding Agency and Grant Number: Hungarian Brain Research Program [2017-1.2.1-NKP-2017-00002]; National Research, Development and Innovation Office [K131893]
            Funding text: This work was supported by Hungarian Brain Research Program Grant 2017-1.2.1-NKP-2017-00002 and National Research, Development and Innovation Office Grant K131893. We thank Peter Foldi, Eva Krizsan, Orsolya Papp, and Erzsebet Gregori for technical assistance and Laszlo Barna, the Nikon Microscopy Center at the Institute of Experimental Medicine, Nikon Austria, and Auro-Science Consulting for providing microscopy support.</comment>
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      <abstractText>Perisomatic inhibition profoundly controls neural function. However, the structural organization of inhibitory circuits giving rise to the perisomatic inhibition in the higher-order cortices is not completely known. Here, we performed a comprehensive analysis of those GABAergic cells in the medial prefrontal cortex (mPFC) that provide inputs onto the somata and proximal dendrites of pyramidal neurons. Our results show that most GABAergic axonal varicosities contacting the perisomatic region of superficial (layer 2/3) and deep (layer 5) pyramidal cells express parvalbumin (PV) or cannabinoid receptor type 1 (CB1). Further, we found that the ratio of PV/CB1 GABAergic inputs is larger on the somatic membrane surface of pyramidal tract neurons in comparison with those projecting to the contralateral hemisphere. Our morphologic analysis of&lt;jats:italic>in vitro&lt;/jats:italic>labeled PV+ basket cells (PVBC) and CCK/CB1+ basket cells (CCKBC) revealed differences in many features. PVBC dendrites and axons arborized preferentially within the layer where their soma was located. In contrast, the axons of CCKBCs expanded throughout layers, although their dendrites were found preferentially either in superficial or deep layers. Finally, using anterograde trans-synaptic tracing we observed that PVBCs are preferentially innervated by thalamic and basal amygdala afferents in layers 5a and 5b, respectively. Thus, our results suggest that PVBCs can control the local circuit operation in a layer-specific manner via their characteristic arborization, whereas CCKBCs rather provide cross-layer inhibition in the mPFC.&lt;/jats:p>&lt;jats:p>&lt;jats:bold>SIGNIFICANCE STATEMENT&lt;/jats:bold>Inhibitory cells in cortical circuits are crucial for the precise control of local network activity. Nevertheless, in higher-order cortical areas that are involved in cognitive functions like decision-making, working memory, and cognitive flexibility, the structural organization of inhibitory cell circuits is not completely understood. In this study we show that perisomatic inhibitory control of excitatory cells in the medial prefrontal cortex is performed by two types of basket cells endowed with different morphologic properties that provide inhibitory inputs with distinct layer specificity on cells projecting to disparate areas. Revealing this difference in innervation strategy of the two basket cell types is a key step toward understanding how they fulfill their distinct roles in cortical network operations.</abstractText>
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				    &lt;/div&gt;
&lt;/div&gt;
&lt;div class=&quot;title&quot;&gt;&lt;a href=&quot;/gui2/?mode=browse&amp;params=publication;34125713&quot; target=&quot;_blank&quot;&gt;Structural organisation of perisomatic inhibition in the mouse medial prefrontal cortex&lt;/a&gt;&lt;/div&gt;    &lt;div&gt;		&lt;span class=&quot;journal-title&quot;&gt;JOURNAL OF NEUROSCIENCE&lt;/span&gt;

        &lt;span class=&quot;journal-issn&quot;&gt;(&lt;a target=&quot;_blank&quot; href=&quot;https://portal.issn.org/resource/ISSN/0270-6474&quot;&gt;0270-6474&lt;/a&gt; &lt;a target=&quot;_blank&quot; href=&quot;https://portal.issn.org/resource/ISSN/1529-2401&quot;&gt;1529-2401&lt;/a&gt;)&lt;/span&gt;:
		&lt;span class=&quot;journal-volume&quot;&gt;43&lt;/span&gt; &lt;span class=&quot;journal-issue&quot;&gt;42&lt;/span&gt;
&lt;span class=&quot;page&quot;&gt;
	pp 6972-6987
			
&lt;/span&gt;		 &lt;span class=&quot;year&quot;&gt;(2023)&lt;/span&gt;  
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&lt;div class=&quot;pub-footer&quot;&gt;
    

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									DOI
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	&lt;OnlyViewableByAuthor&gt;&lt;div class=&quot;ratings&quot;&gt;
				&lt;div class=&quot;journal-subject&quot;&gt;Journal subject: Scopus - Neuroscience (miscellaneous)&amp;nbsp;&amp;nbsp;&amp;nbsp;Rank:&amp;nbsp;Q1&lt;/div&gt;
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	&lt;div class=&quot;publication-citation&quot; style=&quot;margin-left: 0.5cm;&quot;&gt;
		&lt;span title=&quot;&quot; class=&quot;citingPub-count&quot;&gt;Citing papers: 10&lt;/span&gt;
		| Independent citation: 9
		| Self citation: 1
		| Unknown citation: 0
		| Number of citations in WoS: 10 
		|  Number of citations in Scopus:&amp;nbsp;7 
		|  WoS/Scopus assigned:&amp;nbsp;10 
		|  Number of citations with DOI:&amp;nbsp;10 
		
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			Number of cited publications: 33
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    &lt;div class=&quot;mtid&quot;&gt;&lt;span class=&quot;long-pub-mtid&quot;&gt;Publication: 34125713&lt;/span&gt;
    | &lt;span class=&quot;status-data status-APPROVED&quot;&gt; 	Published
  &lt;/span&gt;
        
	
	
Core	 Citing
	
	
    | &lt;span class=&quot;type-subtype&quot;&gt;Journal Article
			( Article
			
			)
		&lt;/span&gt;
      		| &lt;span class=&quot;pub-category&quot;&gt;Scientific&lt;/span&gt;
	| &lt;span class=&quot;publication-sourceOfData&quot;&gt;kézi felvitel&lt;/span&gt;
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&lt;div class=&quot;funder&quot;&gt; Hungarian National Brain Research Program(2017-1.2.1-NKP-2017-00002),    (K131893)   &lt;/div&gt;
&lt;div class=&quot;lastModified&quot;&gt;Last Modified: 2025.11.18. 12:22 Ilona Kósa (MTMT központi Admin, admin)
&lt;/div&gt;


        &lt;div class=&quot;lockedBy&quot;&gt;Centrally managed 2024.04.17. 16:19  Katalin Lévayné Deseő (MTMT Központi admin)
        &lt;/div&gt;


	&lt;pre class=&quot;comment&quot; style=&quot;margin-top: 0; margin-bottom: 0;&quot;&gt;&lt;u&gt;Comments&lt;/u&gt;: Funding Agency and Grant Number: Hungarian Brain Research Program [2017-1.2.1-NKP-2017-00002]; National Research, Development and Innovation Office [K131893]
            Funding text: This work was supported by Hungarian Brain Research Program Grant 2017-1.2.1-NKP-2017-00002 and National Research, Development and Innovation Office Grant K131893. We thank Peter Foldi, Eva Krizsan, Orsolya Papp, ...&lt;/pre&gt;
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