| Literature DB >> 33643001 |
Lars Hildebrandt-Einfeldt1, Kenrick Yap1, Mandy H Paul1, Carolin Stoffer1, Nadine Zahn1, Alexander Drakew1, Maximilian Lenz2, Andreas Vlachos2,3,4, Thomas Deller1.
Abstract
The entorhino-dentate projection, i.e., the perforant pathway, terminates in a highly ordered and laminated fashion in the rodent dentate gyrus (DG): fibers arising from the medial entorhinal cortex (MEC) terminate in the middle molecular layer, whereas fibers arising from the lateral entorhinal cortex (LEC) terminate in the outer molecular layer of the DG. In rats and rabbits, a crossed entorhino-dentate projection exists, which originates from the entorhinal cortex (EC) and terminates in the contralateral DG. In contrast, in mice, such a crossed projection is reportedly absent. Using single and double mouse organotypic entorhino-hippocampal slice cultures, we studied the ipsi- and crossed entorhino-dentate projections. Viral tracing revealed that entorhino-dentate projections terminate with a high degree of lamina-specificity in single as well as in double cultures. Furthermore, in double cultures, entorhinal axons arising from one slice freely intermingled with entorhinal axons originating from the other slice. In single as well as in double cultures, entorhinal axons exhibited a correct topographical projection to the DG: medial entorhinal axons terminated in the middle and lateral entorhinal axons terminated in the outer molecular layer. Finally, entorhinal neurons were virally transduced with Channelrhodopsin2-YFP and stimulated with light, revealing functional connections between the EC and dentate granule cells. We conclude from our findings that entorhino-dentate projections form bilaterally in the mouse hippocampus in vitro and that the mouse DG provides a permissive environment for crossed entorhinal fibers.Entities:
Keywords: calretinin; dentate gyrus; layer-specificity; perforant path transection; species differences; viral tracing
Year: 2021 PMID: 33643001 PMCID: PMC7904698 DOI: 10.3389/fnana.2021.637036
Source DB: PubMed Journal: Front Neuroanat ISSN: 1662-5129 Impact factor: 3.856