Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus
Abstract Background CSF has long been accepted to circulate throughout the subarachnoid space, which lies between the arachnoid and pia maters of the meninges. How the CSF interacts with the cellular components of the developing postnatal meninges including the dura, arachnoid, and pia of both the m...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2024-01-01
|
Series: | Fluids and Barriers of the CNS |
Online Access: | https://doi.org/10.1186/s12987-023-00503-7 |
_version_ | 1797355567819259904 |
---|---|
author | Shelei Pan Joshua P. Koleske Gretchen M. Koller Grace L. Halupnik Abdul-Haq O. Alli Shriya Koneru Dakota DeFreitas Sruthi Ramagiri Jennifer M. Strahle |
author_facet | Shelei Pan Joshua P. Koleske Gretchen M. Koller Grace L. Halupnik Abdul-Haq O. Alli Shriya Koneru Dakota DeFreitas Sruthi Ramagiri Jennifer M. Strahle |
author_sort | Shelei Pan |
collection | DOAJ |
description | Abstract Background CSF has long been accepted to circulate throughout the subarachnoid space, which lies between the arachnoid and pia maters of the meninges. How the CSF interacts with the cellular components of the developing postnatal meninges including the dura, arachnoid, and pia of both the meninges at the surface of the brain and the intracranial meninges, prior to its eventual efflux from the cranium and spine, is less understood. Here, we characterize small and large CSF solute distribution patterns along the intracranial and surface meninges in neonatal rodents and compare our findings to meningeal CSF solute distribution in a rodent model of intraventricular hemorrhage-posthemorrhagic hydrocephalus. We also examine CSF solute interactions with the tela choroidea and its pial invaginations into the choroid plexuses of the lateral, third, and fourth ventricles. Methods 1.9-nm gold nanoparticles, 15-nm gold nanoparticles, or 3 kDa Red Dextran Tetramethylrhodamine constituted in aCSF were infused into the right lateral ventricle of P7 rats to track CSF circulation. 10 min post-1.9-nm gold nanoparticle and Red Dextran Tetramethylrhodamine injection and 4 h post-15-nm gold nanoparticle injection, animals were sacrificed and brains harvested for histologic analysis to identify CSF tracer localization in the cranial and spine meninges and choroid plexus. Spinal dura and leptomeninges (arachnoid and pia) wholemounts were also evaluated. Results There was significantly less CSF tracer distribution in the dura compared to the arachnoid and pia maters in neonatal rodents. Both small and large CSF tracers were transported intracranially to the arachnoid and pia mater of the perimesencephalic cisterns and tela choroidea, but not the falx cerebri. CSF tracers followed a similar distribution pattern in the spinal meninges. In the choroid plexus, there was large CSF tracer distribution in the apical surface of epithelial cells, and small CSF tracer along the basolateral surface. There were no significant differences in tracer intensity in the intracranial meninges of control vs. intraventricular hemorrhage-posthemorrhagic hydrocephalus (PHH) rodents, indicating preserved meningeal transport in the setting of PHH. Conclusions Differential CSF tracer handling by the meninges suggests that there are distinct roles for CSF handling between the arachnoid-pia and dura maters in the developing brain. Similarly, differences in apical vs. luminal choroid plexus CSF handling may provide insight into particle-size dependent CSF transport at the CSF-choroid plexus border. |
first_indexed | 2024-03-08T14:13:01Z |
format | Article |
id | doaj.art-404d7d737ca44f8a9aecfe3a23ac3d73 |
institution | Directory Open Access Journal |
issn | 2045-8118 |
language | English |
last_indexed | 2024-03-08T14:13:01Z |
publishDate | 2024-01-01 |
publisher | BMC |
record_format | Article |
series | Fluids and Barriers of the CNS |
spelling | doaj.art-404d7d737ca44f8a9aecfe3a23ac3d732024-01-14T12:33:18ZengBMCFluids and Barriers of the CNS2045-81182024-01-0121111610.1186/s12987-023-00503-7Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalusShelei Pan0Joshua P. Koleske1Gretchen M. Koller2Grace L. Halupnik3Abdul-Haq O. Alli4Shriya Koneru5Dakota DeFreitas6Sruthi Ramagiri7Jennifer M. Strahle8Department of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisDepartment of Neurosurgery, Washington University School of Medicine, Washington University in St. LouisAbstract Background CSF has long been accepted to circulate throughout the subarachnoid space, which lies between the arachnoid and pia maters of the meninges. How the CSF interacts with the cellular components of the developing postnatal meninges including the dura, arachnoid, and pia of both the meninges at the surface of the brain and the intracranial meninges, prior to its eventual efflux from the cranium and spine, is less understood. Here, we characterize small and large CSF solute distribution patterns along the intracranial and surface meninges in neonatal rodents and compare our findings to meningeal CSF solute distribution in a rodent model of intraventricular hemorrhage-posthemorrhagic hydrocephalus. We also examine CSF solute interactions with the tela choroidea and its pial invaginations into the choroid plexuses of the lateral, third, and fourth ventricles. Methods 1.9-nm gold nanoparticles, 15-nm gold nanoparticles, or 3 kDa Red Dextran Tetramethylrhodamine constituted in aCSF were infused into the right lateral ventricle of P7 rats to track CSF circulation. 10 min post-1.9-nm gold nanoparticle and Red Dextran Tetramethylrhodamine injection and 4 h post-15-nm gold nanoparticle injection, animals were sacrificed and brains harvested for histologic analysis to identify CSF tracer localization in the cranial and spine meninges and choroid plexus. Spinal dura and leptomeninges (arachnoid and pia) wholemounts were also evaluated. Results There was significantly less CSF tracer distribution in the dura compared to the arachnoid and pia maters in neonatal rodents. Both small and large CSF tracers were transported intracranially to the arachnoid and pia mater of the perimesencephalic cisterns and tela choroidea, but not the falx cerebri. CSF tracers followed a similar distribution pattern in the spinal meninges. In the choroid plexus, there was large CSF tracer distribution in the apical surface of epithelial cells, and small CSF tracer along the basolateral surface. There were no significant differences in tracer intensity in the intracranial meninges of control vs. intraventricular hemorrhage-posthemorrhagic hydrocephalus (PHH) rodents, indicating preserved meningeal transport in the setting of PHH. Conclusions Differential CSF tracer handling by the meninges suggests that there are distinct roles for CSF handling between the arachnoid-pia and dura maters in the developing brain. Similarly, differences in apical vs. luminal choroid plexus CSF handling may provide insight into particle-size dependent CSF transport at the CSF-choroid plexus border.https://doi.org/10.1186/s12987-023-00503-7 |
spellingShingle | Shelei Pan Joshua P. Koleske Gretchen M. Koller Grace L. Halupnik Abdul-Haq O. Alli Shriya Koneru Dakota DeFreitas Sruthi Ramagiri Jennifer M. Strahle Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus Fluids and Barriers of the CNS |
title | Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus |
title_full | Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus |
title_fullStr | Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus |
title_full_unstemmed | Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus |
title_short | Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus |
title_sort | postnatal meningeal csf transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage posthemorrhagic hydrocephalus |
url | https://doi.org/10.1186/s12987-023-00503-7 |
work_keys_str_mv | AT sheleipan postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT joshuapkoleske postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT gretchenmkoller postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT gracelhalupnik postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT abdulhaqoalli postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT shriyakoneru postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT dakotadefreitas postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT sruthiramagiri postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus AT jennifermstrahle postnatalmeningealcsftransportisprimarilymediatedbythearachnoidandpiamatersandisnotalteredafterintraventricularhemorrhageposthemorrhagichydrocephalus |