The choroid plexus is a highly vascular specialized structure within the cerebral ventricles that produces most cerebrospinal fluid. It consists of fenestrated capillaries within a connective tissue core covered by specialized choroid plexus epithelial cells derived from ependymal cells, which form the blood-CSF barrier.
The choroid plexus is a highly vascular specialized structure located within the ventricular system of the brain. Its principal function is the production and regulation of cerebrospinal fluid (CSF).
Choroid plexuses are present within the lateral ventricles, third ventricle, and fourth ventricle. They are not present within the cerebral aqueduct or the normal central canal of the spinal cord.
Structurally, each choroid plexus consists of a vascular connective tissue core containing fenestrated capillaries, covered by specialized choroid plexus epithelial cells. Tight junctions between these epithelial cells form the anatomical basis of the blood-CSF barrier.
Choroid plexus tissue projects into the ventricular cavities at specific sites where vascular pia and ventricular lining are closely related.
The distribution differs among the lateral, third, and fourth ventricles.
Within each lateral ventricle, the choroid plexus extends through portions of the body, atrium, and temporal horn.
It is associated with the choroidal fissure, a cleft between the fornix and thalamic or fimbrial structures through which the vascular choroidal tissue is related to the ventricular cavity.
The choroid plexus of the third ventricle is associated with its roof.
It is related to the tela choroidea and vascular structures situated between the third ventricle and overlying deep cerebral structures.
The choroid plexus of the fourth ventricle is associated primarily with the inferior portion of its roof.
It contributes CSF directly to the fourth ventricular cavity, from which CSF can enter the subarachnoid space through the median and lateral apertures.
| Ventricular Region | Choroid Plexus |
|---|---|
| Lateral ventricles | Present in body, atrium and temporal horn |
| Third ventricle | Present along roof |
| Cerebral aqueduct | Absent |
| Fourth ventricle | Present, especially along inferior roof |
| Central canal | Absent |
The choroidal fissure is an important anatomical cleft associated with attachment of the choroid plexus of the lateral ventricle.
It follows a curved course related to the fornix, thalamus, fimbria, and medial temporal structures.
The tela choroidea is a thin vascular membrane formed where pia-related vascular tissue is closely applied to the ventricular lining.
Invagination and specialization of this tissue contribute to formation of the choroid plexus.
The choroid plexus consists of numerous branching folds and villous projections that increase its surface area.
Each projection contains a central vascular connective tissue core covered by a layer of specialized epithelial cells.
The major histological components of the choroid plexus include:
The ventricular surface of the choroid plexus is covered by a single layer of specialized choroid plexus epithelial cells.
These cells are modified ependymal cells and possess structural and transport characteristics suited to controlled secretion of CSF.
The apical surface of choroid plexus epithelial cells faces the ventricular CSF.
Microvilli increase the surface area available for transport, while cellular transport systems regulate movement of ions, water, and other substances between blood-derived interstitial fluid and the ventricular compartment.
Adjacent choroid plexus epithelial cells are connected by tight junctions.
These junctions restrict uncontrolled movement of substances between the cells and are fundamental to the blood-CSF barrier.
The capillaries within the choroid plexus are fenestrated and relatively permeable compared with capillaries forming the blood-brain barrier.
Substances can therefore leave the capillary lumen and enter the choroid plexus stroma more readily, but passage into CSF remains regulated by the epithelial layer.
The blood-CSF barrier is formed primarily by tight junctions between choroid plexus epithelial cells.
It regulates the movement of ions, metabolites, proteins, xenobiotics, and other substances between blood and ventricular CSF.
| Feature | Blood-CSF Barrier | Blood-Brain Barrier |
|---|---|---|
| Principal barrier cells | Choroid plexus epithelial cells | Cerebral capillary endothelial cells |
| Site of tight junctions | Between epithelial cells | Between endothelial cells |
| Underlying capillaries | Fenestrated | Continuous, nonfenestrated |
| Primary interface | Blood and ventricular CSF | Blood and brain interstitial environment |
The choroid plexus produces most of the cerebrospinal fluid within the ventricular system.
CSF formation is an active secretory process involving selective transport of electrolytes across the choroid plexus epithelium, followed by movement of water into the ventricular cavity.
CSF production depends on coordinated transport of ions including sodium, chloride, and bicarbonate across choroid plexus epithelial cells.
Water follows the resulting osmotic gradients through transcellular pathways, producing a clear fluid with a composition distinct from blood plasma.
Normal CSF contains water, electrolytes, glucose, small amounts of protein, and very few cells.
The choroid plexus contributes to maintaining this controlled composition through selective secretion, transport, and clearance mechanisms.
The functions of the choroid plexus extend beyond simple fluid production.
After production by the choroid plexuses, CSF moves through the ventricular system and into the subarachnoid space.
A simplified pathway is:
CSF produced within the lateral ventricles passes through the paired interventricular foramina into the third ventricle.
Additional CSF is produced by the third ventricular choroid plexus.
CSF passes from the third ventricle through the cerebral aqueduct into the fourth ventricle.
The cerebral aqueduct contains no choroid plexus and functions primarily as a narrow connecting channel.
CSF leaves the fourth ventricle primarily through the median aperture and paired lateral apertures.
It then circulates through the subarachnoid cisterns and around the surfaces of the brain and spinal cord.
The choroid plexus is principally associated with CSF production rather than the major routes of CSF return to the circulation.
CSF outflow involves arachnoid granulations and additional drainage pathways associated with meningeal and lymphatic systems.
| Feature | Choroid Plexus | Arachnoid Granulations |
|---|---|---|
| Location | Within ventricles | Project from arachnoid toward dural venous sinuses |
| Primary association | CSF production and regulation | CSF outflow to venous circulation |
| Barrier function | Forms blood-CSF barrier | Participates in CSF drainage |
The choroid plexus has a rich arterial supply derived from choroidal arteries.
Different portions of the ventricular plexuses receive blood from branches of the internal carotid and vertebrobasilar circulations.
The anterior choroidal artery, usually arising from the internal carotid artery, contributes to the choroid plexus of the lateral ventricle, particularly within the temporal horn.
It also supplies several important deep neural structures along its course.
The posterior choroidal arteries generally arise from the posterior cerebral circulation.
Medial and lateral posterior choroidal branches contribute to choroid plexuses of the third and lateral ventricles and supply adjacent deep structures.
The choroid plexus of the fourth ventricle receives arterial contributions from branches of the posterior inferior cerebellar artery and related posterior circulation vessels.
Venous drainage from the choroid plexuses communicates with the deep cerebral venous system.
Veins associated with the lateral and third ventricular plexuses ultimately contribute to deep venous channels such as the internal cerebral veins and related vessels.
The choroid plexus develops at specialized regions where vascular mesenchyme and pia-related tissue become closely associated with the thin ventricular roof.
The epithelial covering is derived from neuroectodermal ventricular lining, while the vascular connective tissue core has mesenchymal contributions.
Cells derived from the neuroepithelial lining differentiate into specialized choroid plexus epithelial cells.
These cells develop tight junctions and transport systems required for formation of the blood-CSF interface.
By controlling the composition of CSF, the choroid plexus contributes to the chemical stability of the central nervous system.
Its transport systems regulate the movement of water, electrolytes, nutrients, metabolites, and selected signaling molecules.
The choroid plexus also functions as an interface between the immune system, blood, and central nervous system.
Its vascular stroma can contain immune cells, while the epithelial barrier regulates movement of cells and molecules into the CSF compartment.
The choroid plexus can be identified on CT and MRI within characteristic ventricular locations.
Because it is highly vascular, it normally enhances after administration of contrast material.
Calcification of portions of the choroid plexus is common, particularly in adults, and is often a normal incidental imaging finding.
Calcification is frequently visible within the atria of the lateral ventricles.
Choroid plexus papilloma is a tumor arising from choroid plexus epithelium.
It can occur within the ventricular system and may cause hydrocephalus through excessive CSF production, obstruction of CSF pathways, or both.
Choroid plexus carcinoma is a malignant choroid plexus epithelial tumor.
It is uncommon and occurs predominantly in children. Its ventricular location can produce symptoms related to increased intracranial pressure and hydrocephalus.
Hydrocephalus results from abnormal accumulation of CSF associated with disturbed CSF circulation, absorption, or, less commonly, excessive production.
Because the choroid plexus continuously secretes CSF, obstruction of ventricular pathways can cause progressive enlargement of ventricles proximal to the obstruction.
Excessive CSF production is an uncommon mechanism of hydrocephalus but may occur with certain choroid plexus tumors.
More commonly, hydrocephalus results from impaired CSF flow or impaired outflow from the intracranial CSF spaces.
The highly vascular nature of the choroid plexus makes it relevant to intraventricular hemorrhage.
Blood entering the ventricular system can interfere with normal CSF circulation and may contribute to secondary hydrocephalus.
Choroid plexus cysts can occur during fetal development and are often detected on prenatal ultrasonography.
Many are transient and resolve during gestation. Their clinical interpretation depends on associated findings and the broader prenatal assessment.
Inflammatory processes affecting the ventricular and meningeal compartments can involve the choroid plexus and alter blood-CSF barrier function.
Changes in epithelial transport and immune signaling may influence the composition of CSF during disease.
The choroid plexus is an important landmark during ventricular and endoscopic neurosurgical procedures.
Within the lateral ventricle, its relationship to the choroidal fissure, fornix, thalamus, and interventricular foramen helps orient the surgeon to deep ventricular anatomy.
The choroid plexus near the interventricular foramen provides a useful anatomical landmark at the junction between the lateral and third ventricles.
This region is closely related to the fornix, thalamus, septal structures, and deep cerebral veins.
| Feature | Key Point |
|---|---|
| Primary function | Production and regulation of CSF |
| Locations | Lateral, third and fourth ventricles |
| Absent from | Cerebral aqueduct and central canal |
| Surface cells | Specialized choroid plexus epithelial cells |
| Capillaries | Fenestrated |
| Barrier | Blood-CSF barrier |
| Barrier junctions | Tight junctions between epithelial cells |
| Major arterial sources | Anterior and posterior choroidal arteries plus posterior circulation branches |
| Imaging feature | Normal contrast enhancement and frequent age-related calcification |
| Major clinical associations | Choroid plexus tumors and hydrocephalus |
The choroid plexus is the principal anatomical structure responsible for producing the fluid environment surrounding and supporting the central nervous system. Its highly vascular core allows close contact with the circulation, while the specialized epithelial covering carefully regulates which substances enter the ventricular CSF.
This organization creates the blood-CSF barrier, which differs structurally from the blood-brain barrier because its tight junctions are located between epithelial cells rather than between capillary endothelial cells.
By producing CSF and regulating its composition, the choroid plexus contributes to mechanical protection, chemical homeostasis, transport, waste handling, and signaling within the central nervous system. Its ventricular location also makes it an important landmark in neuroimaging and neurosurgical anatomy.