Topographic organization in the cerebellar nuclei and inferior olive in relation to cerebellar hemispheric lobules in the mouse: Distinction between crus I and neighboring lobules
- PMID: 37585320
 - DOI: 10.1002/cne.25527
 
Topographic organization in the cerebellar nuclei and inferior olive in relation to cerebellar hemispheric lobules in the mouse: Distinction between crus I and neighboring lobules
Abstract
The parallel closed-loop topographic connections between subareas of the inferior olive (IO), cerebellar cortex, and cerebellar nuclei (CN) define the fundamental modular organization of the cerebellum. The cortical modules or zones are organized into longitudinal zebrin stripes which are extended across transverse cerebellar lobules. However, how cerebellar lobules, which are related to the cerebellar functional localization, are incorporated into the olivo-cortico-nuclear topographic organization has not been fully clarified. In the present study, we analyzed the lobular topography in the CN and IO by making 57 small bidirectional tracer injections in the lateral zebrin-positive stripes equivalent with C2, D1, and D2 zones in every hemispheric lobule in zebrin stripe-visualized mice. C2, D1, and D2 zones were connected to the lateral part of the posterior interpositus nucleus (lPIN), and caudal and rostral parts of the lateral nucleus (cLN, rLN), respectively, and from the rostral part of the medial accessory olive (rMAO), and ventral and dorsal lamellas of the PO (vPO, dPO), respectively, as reported. Within these areas, crus I was specifically connected to the ventral parts of the lPIN, cLN, and rLN, and from the rostrolateral part of the rMAO and the lateral parts of the vPO and dPO. The results indicated that the cerebellar modules have lobule-related subdivisions and that crus I is topographically distinct from other lobules. We speculate that crus I and crus I-connected subdivisions in the CN and IO are involved more in nonmotor functions than other neighboring areas in the mouse.
Keywords: Purkinje cells; RRID:AB_2313920; cerebellar cortex; cerebellar nuclei; inferior olive; lateral cerebellar nucleus; mice; zebrin II.
© 2023 Wiley Periodicals LLC.
References
REFERENCES
- 
    
- Apps, R., & Hawkes, R. (2009). Cerebellar cortical organization: A one-map hypothesis. Nature Reviews. Neuroscience, 10(9), 670-681. https://doi.org/10.1038/nrn2698
 
 - 
    
- Apps, R., Hawkes, R., Aoki, S., Bengtsson, F., Brown, A. M., Chen, G., Ebner, T. J., Isope, P., Jörntell, H., Lackey, E. P., Lawrenson, C., Lumb, B., Schonewille, M., Sillitoe, R. V., Spaeth, L., Sugihara, I., Valera, A., Voogd, J., Wylie, D. R., & Ruigrok, T. J. H. (2018). Cerebellar modules and their role as operational cerebellar processing units. Cerebellum (London, England), 17, 654-682. https://doi.org/10.1007/s12311-018-0952-3
 
 - 
    
- Azizi, S. A., & Woodward, D. J. (1987). Inferior olivary nuclear complex of the rat: Morphology and comments on the principles of organization within the olivocerebellar system. Journal of Comparative Neurology, 263(4), 467-484. https://doi.org/10.1002/cne.902630402
 
 - 
    
- Biswas, M. S., Luo, Y., Sarpong, G. A., & Sugihara, I. (2019). Divergent projections of single pontocerebellar axons to multiple cerebellar lobules in the mouse. Journal of Comparative Neurology, 527(12), 1966-1985. https://doi.org/10.1002/cne.24662
 
 - 
    
- Bostan, A. C., & Strick, P. L. (2013). Cerebellar Outputs in non-human primates: An anatomical perspective using transsynaptic tracers. In M. Manto, J. D. Schmahmann, F. Rossi, D. L. Gruol, & N. Koibuchi (Eds.), Handbook of the cerebellum and cerebellar disorders. Springer. https://doi.org/10.1007/978-94-007-1333-8_25
 
 
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