Preview

谢切诺夫学报

高级搜索

The supraependymal nerve plexus in rats during early postnatal development

https://doi.org/10.47093/2218-7332.2026.17.2.1489

摘要

The neural plexus located on the ependyma’s apical surface of the cerebral ventricles may be an important link in the extra-barrier signal transmission and regulation of the cerebrospinal fluid composition, but to date it remains a poorly understood part of the central nervous system.

Aim. To investigate signs of functional activity of the supraependymal nerve plexus in early postnatal development using immunohistochemical methods.

Materials and methods. Coronal brain sections of adult rats and rats on postnatal days 1, 7, and 10 (n = 16) were used for immunohistochemical analysis. Antibodies to tyrosine hydroxylase, tryptophan hydroxylase, and synaptophysin were used to identify supraependymal fibers and structures exhibiting potential synaptic activity.

Results. There was no immunopositive reaction observed in the supraependymal plexus of neonatal rats regardless of the marker used. Synaptophysin-containing puncta or fibers with varicosities on the surface of ependymal cells were first detected by the end of the first week of postnatal development. Tryptophan hydroxylase-positive structures were also observed at this stage of postnatal development. Fibers and puncta were located throughout the walls of the lateral and third ventricles, with the exception of the infundibular recess. Only on the 10th day of postnatal development were tyrosine hydroxylase-containing granules detected on the apical surface of the ependyma. A double immunofluorescence assay demonstrated that the tryptophan hydroxylase distribution matched with synaptophysin. Moreover, at none of the studied periods were neurons found on the surface of the ependyma.

Conclusion. The supraependymal plexus exhibits the capacity for synaptic transmission and serotonin synthesis by the end of the first week of postnatal development. By the 10th day of postnatal development, supraependymal nerve fibers may participate in catecholaminergic neurotransmission.

关于作者

V. Razenkova
Institute of Experimental Medicine
俄罗斯联邦


O. Kirik
Institute of Experimental Medicine
俄罗斯联邦


D. Korzhevskii
Institute of Experimental Medicine
俄罗斯联邦


参考

1. Martínez P.M., de Weerd H. The fine structure of the ependymal surface of the recessus infundibularis in the rat. Anat Embryol (Berl). 1977 Dec; 151(3): 241–265. https://doi.org/10.1007/BF00318929. PMID: 603079

2. Richards J.G., Lorez H.P., Colombo V.E., et al. Demonstration of supra-ependymal 5-HT nerve fibres in human brain and their immunohistochemical identification in rat brain. J Physiol (Paris). 1981; 77(2–3): 219–224. PMID: 7026769

3. Rodríguez P., Bouchaud C. The supra-ependymal innervation is not responsible for the repression of tight junctions in the rat cerebral ependyma. Neurobiology (Bp). 1996; 4(3): 185–201. PMID: 9044345

4. Richards J.G., Lorez H.P., Colombo V.E., et al. Supraependymal nerve fibres in human brain: correlative transmission and scanning electron microscopical and fluorescence histochemical studies. Neuroscience. 1980; 5(8): 1489–1502. https://doi.org/10.1016/0306-4522(80)90011-1. PMID: 7402482

5. Lorez H.P., Richards J.G. Supra-ependymal serotoninergic nerves in mammalian brain: morphological, pharmacological and functional studies. Brain Res Bull. 1982 Jul-Dec; 9(1–6): 727–741. https://doi.org/10.1016/0361-9230(82)90179-4. PMID: 6184136

6. Michaloudi H.C., Papadopoulos G.C. Catecholaminergic and serotoninergic fibres innervate the ventricular system of the hedgehog CNS. J Anat. 1996 Oct; 189(Pt 2): 273–283. PMID: 8886949

7. Разенкова В.А., Кирик О.В. Синаптофизин в супраэпендимных структурах головного мозга крысы. Цитология. 2023; 65(4): 348–353. https://doi.org/10.31857/S0041377123040107. EDN: ZKYDBB

8. Troshev D., Bannikova A., Blokhin V., et al. Striatal neurons partially expressing a dopaminergic phenotype: functional significance and regulation. Int J Mol Sci. 2022 Sep; 23(19): 11054. https://doi.org/10.3390/ijms231911054. PMID: 36232359

9. Robinson S.R., Noone D.F., O’Dowd B.S. Ependymocytes and supra-ependymal axons in rat brain contain glutamate. Glia. 1996 Aug; 17(4): 345–348. https://doi.org/10.1002/(SICI)1098-1136(199608)17:4<345::AID-GLIA9>3.0.CO;2-Y. PMID: 8856331. EDN: AVNPVY

10. Hennou S., Khalilov I., Diabira D., et al. Early sequential formation of functional GABA(A) and glutamatergic synapses on CA1 interneurons of the rat foetal hippocampus. Eur J Neurosci. 2002 Jul; 16(2): 197–208. https://doi.org/10.1046/j.14609568.2002.02073.x. PMID: 12169102

11. Колос Е.А., Григорьев И.П., Коржевский Д.Э. Маркер синаптических контактов – синаптофизин. Морфология. 2015; 147(1): 78–82. EDN: TIJLST

12. Sarnat H.B., Born D.E. Synaptophysin immunocytochemistry with thermal intensification: a marker of terminal axonal maturation in the human fetal nervous system. Brain Dev. 1999 Jan; 21(1): 41–50. https://doi.org/10.1016/s0387-7604(98)00068-0. PMID: 10082252

13. Leclerc N., Beesley P.W., Brown I., et al. Synaptophysin expression during synaptogenesis in the rat cerebellar cortex. J Comp Neurol. 1989 Feb; 280(2): 197–212. https://doi.org/10.1002/cne.902800204. PMID: 2494237

14. Ovtscharoff W., Bergmann M., Marquèze-Pouey B., et al. Ontogeny of synaptophysin and synaptoporin in the central nervous system: differential expression in striatal neurons and their afferents during development. Brain Res Dev Brain Res. 1993 Apr; 72(2): 219–225. https://doi.org/10.1016/0165-3806(93)90186-e. PMID: 8485845

15. Dehorter N., Vinay L., Hammond C., Ben-Ari Y. Timing of developmental sequences in different brain structures: physiological and pathological implications. Eur J Neurosci. 2012 Jun; 35(12): 1846–1856. https://doi.org/10.1111/j.1460-9568.2012.08152.x. PMID: 22708595. EDN: PGKMRJ

16. Naskar S., Narducci R., Balzani E., et al. The development of synaptic transmission is time-locked to early social behaviors in rats. Nat Commun. 2019 Mar; 10(1): 1195. https://doi.org/10.1038/s41467-019-09156-3. PMID: 30867422. EDN: REVGHL

17. Li X., Wang S., Zhang D., et al. The periaxonal space as a conduit for cerebrospinal fluid flow to peripheral organs. Proc Natl Acad Sci USA. 2024 Nov; 121(45): e2400024121. https://doi.org/10.1073/pnas.2400024121. Epub 2024 Nov 1. PMID: 39485799. EDN: AQVPEZ

18. Meister B., Hökfelt T., Tsuruo Y., et al. DARPP-32, a dopamine- and cyclic AMP-regulated phosphoprotein in tanycytes of the mediobasal hypothalamus: distribution and relation to dopamine and luteinizing hormone-releasing hormone neurons and other glial elements. Neuroscience. 1988 Nov; 27(2): 607–622. https://doi.org/10.1016/0306-4522(88)90292-8. PMID: 2905789

19. Murtazina A.R., Bondarenko N.S., Pronina T.S., et al. A comparative analysis of CSF and the blood levels of monoamines as neurohormones in rats during ontogenesis. Acta Naturae. 2021 OctDec; 13(4): 89–97. https://doi.org/10.32607/actanaturae.11516. PMID: 35127152. EDN: VKGBIM

20. Tong C.K., Cebrián-Silla A., Paredes M.F., et al. Axons take a dive: specialized contacts of serotonergic axons with cells in the walls of the lateral ventricles in mice and humans. Neurogenesis (Austin). 2014 Jan; 1(1): e29341. https://doi.org/10.4161/neur.29341. PMID: 26413556

21. Cupédo R.N.J. The surface ultrastructure of the habenular complex of the rat. Anat Embryol (Berl). 1977 Dec; 152(1): 43–64. https://doi.org/10.1007/BF00341434. PMID: 605996

22. Cupédo R.N.J., de Weerd H. Serotonergic intraventricular axons in the habenular region. Phagocytosis after induced degeneration. Anat Embryol (Berl). 1980; 158(2): 213–226. https://doi.org/10.1007/BF00315907. PMID: 7356178

23. Sugiyama E., Guerrini M.M., Honda K., et al. Detection of a high-turnover serotonin circuit in the mouse brain using mass spectrometry imaging. iScience. 2019 Oct; 20: 359–372. https://doi.org/10.1016/j.isci.2019.09.036. Epub 2019 Sep 27. PMID: 31614319

24. Kalinina T.S., Dygalo N.N. Development of the noradrenergic system of the rat brain after prenatal exposure to corticosterone. Biology Bulletin. 2013; 40(6): 545–549. https://doi.org/10.1134/S1062359013040043. EDN: SKZMQN

25. Сухарева Е.В., Калинина Т.С., Булыгина В.В., Дыгало Н.Н. Тирозингидроксилаза мозга и ее регуляция глюкокортикоидами. Вавиловский журнал генетики и селекции. 2016; 20(2): 212–219. https://doi.org/10.18699/VJ16.156. EDN: WLVJZL

26. García-González D., Khodosevich K., Watanabe Y., et al. Serotonergic projections govern postnatal neuroblast migration. Neuron. 2017 May; 94(3): 534–549.e9. https://doi.org/10.1016/j.neuron.2017.04.013. PMID: 28472655

27. Chang V.N., Ogelman R., Vargas R.S., Oh W.C. Serotonergic modulation of excitatory synapse development and plasticity. Mol Cells. 2026 May; 49(5): 100346. https://doi.org/10.1016/j.mocell.2026.100346. Epub 2026 Mar 10. PMID: 41819288. EDN: PXVANM

28. Udoh U.G., Bruno J.R., Osborn P.O., Pratt K.G. Serotonin strengthens a developing glutamatergic synapse through a PI3Kdependent mechanism. J Neurosci. 2024 Feb; 44(6): e1260232023. https://doi.org/10.1523/JNEUROSCI.1260-23.2023. PMID: 38169457. EDN: TKWRLG

29. Razenkova V.A., Korzhevskii D.E. Catecholaminergic structures of the rat subfornical organ. Cell and Tissue Biology. 2022; 16(6): 568–575. https://doi.org/10.1134/S1990519X22060062. EDN: NLALOY


评论

浏览: 27

JATS XML

ISSN 2218-7332 (Print)
ISSN 2658-3348 (Online)