Distribution, number, and certain neurochemical identities of infracortical white matter neurons in the brains of three megachiropteran bat species
- PMID: 32103488
- DOI: 10.1002/cne.24894
Distribution, number, and certain neurochemical identities of infracortical white matter neurons in the brains of three megachiropteran bat species
Abstract
A large population of infracortical white matter neurons, or white matter interstitial cells (WMICs), are found within the subcortical white matter of the mammalian telencephalon. We examined WMICs in three species of megachiropterans, Megaloglossus woermanni, Casinycteris argynnis, and Rousettus aegyptiacus, using immunohistochemical and stereological techniques. Immunostaining for neuronal nuclear marker (NeuN) revealed substantial numbers of WMICs in each species-M. woermanni 124,496 WMICs, C. argynnis 138,458 WMICs, and the larger brained R. aegyptiacus having an estimated WMIC population of 360,503. To examine the range of inhibitory neurochemical types we used antibodies against parvalbumin, calbindin, calretinin, and neural nitric oxide synthase (nNOS). The calbindin and nNOS immunostained neurons were the most commonly observed, while those immunoreactive for calretinin and parvalbumin were sparse. The proportion of WMICs exhibiting inhibitory neurochemical profiles was ~26%, similar to that observed in previously studied primates. While for the most part the WMIC population in the megachiropterans studied was similar to that observed in other mammals, the one feature that differed was the high proportion of WMICs immunoreactive to calbindin, whereas in primates (macaque monkey, lar gibbon and human) the highest proportion of inhibitory WMICs contain calretinin. Interestingly, there appears to be an allometric scaling of WMIC numbers with brain mass. Further quantitative comparative work across more mammalian species will reveal the developmental and evolutionary trends associated with this infrequently studied neuronal population.
Keywords: RRID: AB_10000321; RRID: AB_10000340; RRID: AB_10000343; RRID: AB_11204707; RRID: AB_91824; bat brain; cortical evolution; immunohistochemistry; white matter interstitial cells; white matter neurons.
© 2020 Wiley Periodicals, Inc.
Similar articles
-
The distribution, number, and certain neurochemical identities of infracortical white matter neurons in the brains of a southern lesser galago, a black-capped squirrel monkey, and a crested macaque.J Comp Neurol. 2021 Nov;529(16):3676-3708. doi: 10.1002/cne.25216. Epub 2021 Jul 23. J Comp Neurol. 2021. PMID: 34259349
-
The distribution, number, and certain neurochemical identities of infracortical white matter neurons in a lar gibbon (Hylobates lar) brain.J Comp Neurol. 2019 Jul 1;527(10):1633-1653. doi: 10.1002/cne.24545. Epub 2018 Oct 30. J Comp Neurol. 2019. PMID: 30378128 Free PMC article.
-
The distribution, number, and certain neurochemical identities of infracortical white matter neurons in a chimpanzee (Pan troglodytes) brain.J Comp Neurol. 2021 Oct;529(14):3429-3452. doi: 10.1002/cne.25202. Epub 2021 Jul 1. J Comp Neurol. 2021. PMID: 34180538
-
Cellular distribution of the calcium-binding proteins parvalbumin, calbindin, and calretinin in the neocortex of mammals: phylogenetic and developmental patterns.J Chem Neuroanat. 1999 Feb;16(2):77-116. doi: 10.1016/s0891-0618(98)00065-9. J Chem Neuroanat. 1999. PMID: 10223310 Review.
-
Not all brains are made the same: new views on brain scaling in evolution.Brain Behav Evol. 2011;78(1):22-36. doi: 10.1159/000327318. Epub 2011 Jun 17. Brain Behav Evol. 2011. PMID: 21691045 Review.
Cited by
-
Hidden in the white matter: Current views on interstitial white matter neurons.Neuroscientist. 2025 Aug;31(4):381-408. doi: 10.1177/10738584241282969. Epub 2024 Oct 4. Neuroscientist. 2025. PMID: 39365761 Free PMC article. Review.
-
The brain of the tree pangolin (Manis tricuspis). IX. The pallial telencephalon.J Comp Neurol. 2022 Oct;530(15):2645-2691. doi: 10.1002/cne.25349. Epub 2022 May 27. J Comp Neurol. 2022. PMID: 35621013 Free PMC article.
References
REFERENCES
-
- Adrio, F., Rodriguez-Moldes, I., & Anadon, R. (2011). Distribution of glycine immunoreactivity in the brain of the Siberian sturgeon (Acipenser baeri): Comparison with γ-aminobutyric acid. Journal of Comparative Neurology, 519, 1115-1142. https://doi.org/10.1002/cne.22556
-
- Akbarian, S., Kim, J. J., Potkin, S. G., Hetrick, W. P., Bunney, W. E., & Jones, E. G. (1996). Maldistribution of interstitial neurons in prefrontal white matter of the brains of schizophrenic patients. Archives of General Psychiatry, 53, 425-436. https://doi.org/10.1001/archpsyc.1996.01830050061010
-
- Amaral, D. G., Mills Schumann, C., & Wu Nordahl, C. (2008). Neuroanatomy of autism. Trends in Neurosciences, 31, 137-145. https://doi.org/10.1016/j.tins.2007.12.005
-
- Angoulvant, D., & Bejan-Angoulvant, T. (2017). False positive results in preclinical research. Thérapie, 72, 411-413. https://doi.org/10.1016/j.therap.2016.06.001
-
- Arnason, U., Adegoke, J. A., Bodin, K., Born, E. W., Esa, Y. B., Gullberg, A., … Janke, A. (2002). Mammalian mitogenomic relationships and the root of the eutherian tree. Proceedings of the National Academy of Science USA, 99, 8151-8156. https://doi.org/10.1073/pnas.102164299
Publication types
MeSH terms
Grants and funding
- BB/F003285/1/BB_/Biotechnology and Biological Sciences Research Council/United Kingdom
- G0700377/MRC_/Medical Research Council/United Kingdom
- G00900901/MRC_/Medical Research Council/United Kingdom
- G0300200/MRC_/Medical Research Council/United Kingdom
- G0900901/MRC_/Medical Research Council/United Kingdom
LinkOut - more resources
Full Text Sources
Miscellaneous