Abstract
Background: The choroid plexus epithelium (CPE) is a lobed neuro-epithelial structure that forms the outer blood-brain barrier. The CPE protrudes into the brain ventricles and produces the cerebrospinal fluid (CSF), which is crucial for brain homeostasis. Malfunction of the CPE is possibly implicated in disorders like Alzheimer disease, hydrocephalus or glaucoma. To study human genetic diseases and potential new therapies, mouse models are widely used. This requires a detailed knowledge of similarities and differences in gene expression and functional annotation between the species. The aim of this study is to analyze and compare gene expression and functional annotation of healthy human and mouse CPE. Methods: We performed 44k Agilent microarray hybridizations with RNA derived from laser dissected healthy human and mouse CPE cells. We functionally annotated and compared the gene expression data of human and mouse CPE using the knowledge database Ingenuity. We searched for common and species specific gene expression patterns and function between human and mouse CPE. We also made a comparison with previously published CPE human and mouse gene expression data. Results: Overall, the human and mouse CPE transcriptomes are very similar. Their major functionalities included epithelial junctions, transport, energy production, neuro-endocrine signaling, as well as immunological, neurological and hematological functions and disorders. The mouse CPE presented two additional functions not found in the human CPE: carbohydrate metabolism and a more extensive list of (neural) developmental functions. We found three genes specifically expressed in the mouse CPE compared to human CPE, being ACE, PON1 and TRIM3 and no human specifically expressed CPE genes compared to mouse CPE. Conclusion: Human and mouse CPE transcriptomes are very similar, and display many common functionalities. Nonetheless, we also identified a few genes and pathways which suggest that the CPE between mouse and man differ with respect to transport and metabolic functions.
Original language | English |
---|---|
Article number | e83345 |
Journal | PLoS ONE |
Volume | 8 |
Issue number | 12 |
DOIs | |
Publication status | Published - 31 Dec 2013 |
Bibliographical note
Funding:
This study was supported by grants from the General Dutch Foundation Preventing Blindness (ANVVB), National Foundation for Blinds and Low Vision
(LSBS), Foundation Blinden-Penning, Foundation Glaucoomfonds, Rotterdam Foundation of Blinds and the Professor Mulder Foundation (all together cooperated
by UitZicht, project # UitZicht2008-7). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Janssen, S. F., Van Der Spek, S. J. F., Ten Brink, J. B., Essing, A. H. W., Gorgels, T. G. M. F., Van Der Spek, P. J., Jansonius, N. M., & Bergen, A. A. B. (2013). Gene expression and functional annotation of the human and mouse choroid plexus epithelium. PLoS ONE, 8(12), [e83345]. https://doi.org/10.1371/journal.pone.0083345
Janssen, Sarah F. ; Van Der Spek, Sophie J.F. ; Ten Brink, Jacoline B. et al. / Gene expression and functional annotation of the human and mouse choroid plexus epithelium. In: PLoS ONE. 2013 ; Vol. 8, No. 12.
@article{154d789e824944218d0ffdbeb376e918,
title = "Gene expression and functional annotation of the human and mouse choroid plexus epithelium",
abstract = "Background: The choroid plexus epithelium (CPE) is a lobed neuro-epithelial structure that forms the outer blood-brain barrier. The CPE protrudes into the brain ventricles and produces the cerebrospinal fluid (CSF), which is crucial for brain homeostasis. Malfunction of the CPE is possibly implicated in disorders like Alzheimer disease, hydrocephalus or glaucoma. To study human genetic diseases and potential new therapies, mouse models are widely used. This requires a detailed knowledge of similarities and differences in gene expression and functional annotation between the species. The aim of this study is to analyze and compare gene expression and functional annotation of healthy human and mouse CPE. Methods: We performed 44k Agilent microarray hybridizations with RNA derived from laser dissected healthy human and mouse CPE cells. We functionally annotated and compared the gene expression data of human and mouse CPE using the knowledge database Ingenuity. We searched for common and species specific gene expression patterns and function between human and mouse CPE. We also made a comparison with previously published CPE human and mouse gene expression data. Results: Overall, the human and mouse CPE transcriptomes are very similar. Their major functionalities included epithelial junctions, transport, energy production, neuro-endocrine signaling, as well as immunological, neurological and hematological functions and disorders. The mouse CPE presented two additional functions not found in the human CPE: carbohydrate metabolism and a more extensive list of (neural) developmental functions. We found three genes specifically expressed in the mouse CPE compared to human CPE, being ACE, PON1 and TRIM3 and no human specifically expressed CPE genes compared to mouse CPE. Conclusion: Human and mouse CPE transcriptomes are very similar, and display many common functionalities. Nonetheless, we also identified a few genes and pathways which suggest that the CPE between mouse and man differ with respect to transport and metabolic functions.",
author = "Janssen, {Sarah F.} and {Van Der Spek}, {Sophie J.F.} and {Ten Brink}, {Jacoline B.} and Essing, {Anke H.W.} and Gorgels, {Theo G.M.F.} and {Van Der Spek}, {Peter J.} and Jansonius, {Nomdo M.} and Bergen, {Arthur A.B.}",
note = "Funding: This study was supported by grants from the General Dutch Foundation Preventing Blindness (ANVVB), National Foundation for Blinds and Low Vision (LSBS), Foundation Blinden-Penning, Foundation Glaucoomfonds, Rotterdam Foundation of Blinds and the Professor Mulder Foundation (all together cooperated by UitZicht, project # UitZicht2008-7). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.",
year = "2013",
month = dec,
day = "31",
doi = "10.1371/journal.pone.0083345",
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Janssen, SF, Van Der Spek, SJF, Ten Brink, JB, Essing, AHW, Gorgels, TGMF, Van Der Spek, PJ, Jansonius, NM & Bergen, AAB 2013, 'Gene expression and functional annotation of the human and mouse choroid plexus epithelium', PLoS ONE, vol. 8, no. 12, e83345. https://doi.org/10.1371/journal.pone.0083345
Gene expression and functional annotation of the human and mouse choroid plexus epithelium. / Janssen, Sarah F.; Van Der Spek, Sophie J.F.; Ten Brink, Jacoline B. et al.
In: PLoS ONE, Vol. 8, No. 12, e83345, 31.12.2013.
Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - Gene expression and functional annotation of the human and mouse choroid plexus epithelium
AU - Janssen, Sarah F.
AU - Van Der Spek, Sophie J.F.
AU - Ten Brink, Jacoline B.
AU - Essing, Anke H.W.
AU - Gorgels, Theo G.M.F.
AU - Van Der Spek, Peter J.
AU - Jansonius, Nomdo M.
AU - Bergen, Arthur A.B.
N1 - Funding: This study was supported by grants from the General Dutch Foundation Preventing Blindness (ANVVB), National Foundation for Blinds and Low Vision(LSBS), Foundation Blinden-Penning, Foundation Glaucoomfonds, Rotterdam Foundation of Blinds and the Professor Mulder Foundation (all together cooperatedby UitZicht, project # UitZicht2008-7). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
PY - 2013/12/31
Y1 - 2013/12/31
N2 - Background: The choroid plexus epithelium (CPE) is a lobed neuro-epithelial structure that forms the outer blood-brain barrier. The CPE protrudes into the brain ventricles and produces the cerebrospinal fluid (CSF), which is crucial for brain homeostasis. Malfunction of the CPE is possibly implicated in disorders like Alzheimer disease, hydrocephalus or glaucoma. To study human genetic diseases and potential new therapies, mouse models are widely used. This requires a detailed knowledge of similarities and differences in gene expression and functional annotation between the species. The aim of this study is to analyze and compare gene expression and functional annotation of healthy human and mouse CPE. Methods: We performed 44k Agilent microarray hybridizations with RNA derived from laser dissected healthy human and mouse CPE cells. We functionally annotated and compared the gene expression data of human and mouse CPE using the knowledge database Ingenuity. We searched for common and species specific gene expression patterns and function between human and mouse CPE. We also made a comparison with previously published CPE human and mouse gene expression data. Results: Overall, the human and mouse CPE transcriptomes are very similar. Their major functionalities included epithelial junctions, transport, energy production, neuro-endocrine signaling, as well as immunological, neurological and hematological functions and disorders. The mouse CPE presented two additional functions not found in the human CPE: carbohydrate metabolism and a more extensive list of (neural) developmental functions. We found three genes specifically expressed in the mouse CPE compared to human CPE, being ACE, PON1 and TRIM3 and no human specifically expressed CPE genes compared to mouse CPE. Conclusion: Human and mouse CPE transcriptomes are very similar, and display many common functionalities. Nonetheless, we also identified a few genes and pathways which suggest that the CPE between mouse and man differ with respect to transport and metabolic functions.
AB - Background: The choroid plexus epithelium (CPE) is a lobed neuro-epithelial structure that forms the outer blood-brain barrier. The CPE protrudes into the brain ventricles and produces the cerebrospinal fluid (CSF), which is crucial for brain homeostasis. Malfunction of the CPE is possibly implicated in disorders like Alzheimer disease, hydrocephalus or glaucoma. To study human genetic diseases and potential new therapies, mouse models are widely used. This requires a detailed knowledge of similarities and differences in gene expression and functional annotation between the species. The aim of this study is to analyze and compare gene expression and functional annotation of healthy human and mouse CPE. Methods: We performed 44k Agilent microarray hybridizations with RNA derived from laser dissected healthy human and mouse CPE cells. We functionally annotated and compared the gene expression data of human and mouse CPE using the knowledge database Ingenuity. We searched for common and species specific gene expression patterns and function between human and mouse CPE. We also made a comparison with previously published CPE human and mouse gene expression data. Results: Overall, the human and mouse CPE transcriptomes are very similar. Their major functionalities included epithelial junctions, transport, energy production, neuro-endocrine signaling, as well as immunological, neurological and hematological functions and disorders. The mouse CPE presented two additional functions not found in the human CPE: carbohydrate metabolism and a more extensive list of (neural) developmental functions. We found three genes specifically expressed in the mouse CPE compared to human CPE, being ACE, PON1 and TRIM3 and no human specifically expressed CPE genes compared to mouse CPE. Conclusion: Human and mouse CPE transcriptomes are very similar, and display many common functionalities. Nonetheless, we also identified a few genes and pathways which suggest that the CPE between mouse and man differ with respect to transport and metabolic functions.
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Janssen SF, Van Der Spek SJF, Ten Brink JB, Essing AHW, Gorgels TGMF, Van Der Spek PJ et al. Gene expression and functional annotation of the human and mouse choroid plexus epithelium. PLoS ONE. 2013 Dec 31;8(12):e83345. doi: 10.1371/journal.pone.0083345
FAQs
What is the function of the choroid plexus in the brain? ›
One of the primary functions is to produce cerebrospinal fluid (CSF) via the ependymal cells that line the ventricles of the brain. Secondly, the choroid plexus serves as a barrier in the brain separating the blood from the CSF, known as the blood-CSF barrier.
Where are the choroid plexuses found and what is their function? ›The choroid plexus (ChP) is a secretory tissue found in each of the brain ventricles, the main function of which is to produce cerebrospinal fluid (CSF).
What is choroid plexus epithelial cells? ›Choroid plexus epithelial cells (CPEpiC) play a central role in restricting the passage of molecules and ions between the brain and CSF by the junctional complexes between neighboring cells. They also have a special cellular structure, and channel and transporter protein expression well-adapted for CSF secretion.
What are the characteristics of the choroid plexuses? ›Choroid Plexus Anomalies
The choroid plexus is a vascular convolute, consisting of epithelial cells (a type of microglia), fenestrated blood vessels, and stroma, which lie in the ventricular system of the brain. It is the main source of cerebrospinal fluid (CSF) and actively regulates the constituents in CSF.
What is the function of the choroid plexus? The choroid plexus produces cerebrospinal fluid.
What are two functions of the choroid layer in the eye? ›The choroid has several functions: Its vasculature is the major supply for the outer retina; impairment of the flow of oxygen from choroid to retina may cause Age-Related Macular Degeneration. The choroidal blood flow, which is as great as in any other organ, may also cool and warm the retina.
Where are the choroid plexuses found? ›The choroid plexuses, found in the lateral, third and fourth ventricles of the brain (adjacent to the embryonic dorsal midline in the hindbrain, diencephalon, and telencephalon, respectively) are epithelial tissue masses highly vascularized with fenestrated blood vessels (Figure 1).
What is the physiology of the choroid plexus? ›The choroid plexuses (CPs) are leaf-like highly vascular structures laying in the ventricles. The main function of choroid plexuses is the production of the cerebrospinal fluid (CSF).
What are choroid plexuses composed of? ›Composition. The tissue of the choroid plexus consists of both columnar cuboidal epithelial cells and specialized cells called ependyma. The ependyma are ciliated, meaning they have tiny hair-like projections on the outside of the cell as well as microvilli (projections that work to absorb CSF).
What is the role of the choroid plexus in health and disease? ›The choroid plexus acts as an immunological niche where several types of peripheral immune cells can be found within the stroma including dendritic cells, macrophages, and T cells. Including the epithelia cells, these cells perform immunosurveillance, detecting pathogens and changes in the cytokine milieu.
What is the choroid plexus also known as? ›
The choroid plexus, or plica choroidea, is a plexus of cells that arises from the tela choroidea in each of the ventricles of the brain. Regions of the choroid plexus produce and secrete most of the cerebrospinal fluid (CSF) of the central nervous system.
What do epithelial cells do in the brain? ›The cerebral endothelium forms the largest barrier in the brain, the BBB, while epithelial cells of the choroid plexus form the blood–CSF barrier, and the avascular arachnoid epithelium lies under the dura and completely encases the brain, forming the CSF–blood barrier.
What is the structure and function of choroid? ›Choroid is the vascular layer of the eye. Also referred to as choroid coat or choroidea, it is a thin layer of tissue which is part of the middle layer of the eye wall, found between the sclera and the retina. The choroid is filled with blood vessels, which brings nutrients and oxygen to the outer layers of the retina.
What is a characteristic feature of choroid layer of human eye? ›The choroid is a layer of eyeball. The eyeball has three coats namely sclera, choroid, and retina. The choroid is middle dark pigmented thin vascular layer of the eyeball and is characterized by the presence of many blood vessels.
What is choroid description and function? ›(KOR-oyd) A thin layer of tissue that is part of the middle layer of the wall of the eye, between the sclera (white outer layer of the eye) and the retina (the inner layer of nerve tissue at the back of the eye). The choriod is filled with blood vessels that bring oxygen and nutrients to the eye.
How is the choroid in the human eye adapted to its function? ›The choroid blocks the internal reflection of light into the eye, contains blood vessels that supply oxygen, nutrients and remove metabolic waste from the eye. The yellow spot of the eye gives accurate visual activity.
What do the choroid plexuses produce ____________________ that helps protects the brain? ›Cerebrospinal fluid is made by tissue called the choroid plexus in the ventricles (hollow spaces) in the brain. Also called CSF.
What are two functions of the choroid quizlet? ›- Nourishment/waste removal of the outer 1/3rd of the retina.
- Thermoregulation (heat dissipation during visual processing)
- Conduit for blood vessels & nerves.
- Absorption of excess light.
Photoreceptors There are two main types of light-sensitive cell in the eye: rods and cones. Rods enable vision in poor light, whereas cones are responsible for colour vision.
What is the histology of the choroid? ›Structure/Histology
The choroid is composed of loose connective tissue containing numerous fibroblasts and other connective tissue cells. The layer closest to the sclera is a layer of pigmented melanocytes, which gives the membrane a black color.
What are the three layers of the eye functions? ›
The cornea and lens bend light so it passes through the vitreous gel in the back chamber of the eye and is projected onto the retina. The retina converts light to electrical impulses. The optic nerve carries these electrical impulses to the brain, which converts them into the visual images that you see.
What is the choroid plexus in simple terms? ›A network of blood vessels and cells in the ventricles (fluid-filled spaces) of the brain. The blood vessels are covered by a thin layer of cells that make cerebrospinal fluid.
Are there neurons in choroid plexus? ›In addition to the core cell types shown above, the researchers found several neuronal subtypes. “Typically, the choroid plexus is not thought to have too many neurons,” says Lehtinen. “What they're doing in the choroid plexus is still up for discussion and experimentation.”
How many choroid plexus are in the brain? ›The choroid plexuses are four modified epithelial structures suspended inside the cerebral ventricles. There are two lateral ventricular choroid plexuses, the third ventricular choroid plexus and the fourth ventricular (hindbrain) choroid plexus (Figure 2).
What is the blood supply to the choroid plexus? ›The choroid plexus of the lateral ventricles are supplied by the anterior choroidal arteries (branch of internal carotid artery) and the lateral posterior choroidal arteries (branch of the posterior cerebral artery).
What are the three structures of the choroid? ›The choroid is a thin, pigmented vascular network consisting of three layers (from inner to outer): choriocapillaris, stroma, and lamina fusca. The choriocapillaris provides nutrients to the RPE and the outer third of the retina.
What is the histology of the normal choroid plexus? ›Normal Histology. Normal choroid plexus, with an epithelial layer around a stroma with prominent blood vessels. This is where the cerebrospinal fluid is formed. The ependymal cells lining the ventricle are present at the left.
How does choroid plexus produce CSF? ›The epithelial cells of the choroid plexus secrete cerebrospinal fluid (CSF), by a process that involves the movement of Na(+), Cl(-) and HCO(3)(-) from the blood to the ventricles of the brain. This creates the osmotic gradient, which drives the secretion of H(2)O.
Is choroid plexus a cell? ›Choroid plexus cells are modified ependymal cells that cover the capillary loops responsible for production of cerebrospinal fluid (CSF). The cells form a single layer of cuboidal epithelium, the slight apical bulge of which resembles a set of cobblestones. Choroid plexus cells are found in all of the ventricles.
Does choroid plexus have blood-brain barrier? ›The choroid plexuses are the main structures that comprise the blood-CSF barrier, the other contributors being the arachnoid and arachnoid villi on the outer surface of the brain (Wright, 1978; and for review see Davson and Segal, 1996).
What is the most important function of epithelial tissue? ›
There are three primary functions of epithelial tissue: serving as a protective barrier, secreting substances, and absorbing substances. The main function of specific tissues varies by the specific location and type of cell. Protective barriers are typically formed by stratified epithelium and goblet cells.
What are the five most important functions of epithelial tissue? ›They perform a variety of functions that include protection, secretion, absorption, excretion, filtration, diffusion, and sensory reception.
What happens when epithelial cells are damaged? ›Damaged epithelial cells stimulate the release of more pro-inflammatory chemokines/cytokines and DAMPs, exacerbating epithelial cell damage and death.
What are the characteristics of the choroid plexus quizlet? ›The choroid plexus is a highly folded membrane, and its surface is covered by a specialized cuboidal layer of epithelium, which differs from the ciliated ependymal cells that line most of the ventricular surface.
Why does choroid have pigment? ›Choroidal pigmentation is largely caused by melanin pigment within choroidal melanocytes. Individuals with dark racial pigmentation generally have very heavy choroidal pigmentation and are at extremely low risk of uveal melanoma.
What are the layers of choroid histology? ›Histologically, the choroid is divided into five layers, starting from the retina to the sclera ( Fig. 3.2 ): (1) Bruch's membrane; (2) choriocapillaris; two layers of vasculature—(3) Sattler's layer; (4) Haller's layer—and (5) suprachoroidea.
What does the thick part of the choroid layer form? ›The choroid layer is thin in the posterior two-thirds of the eye ball, but it becomes thick in the anterior part to form the ciliary body.
What are some facts about the choroid? ›The choroid is the layer of blood vessels and connective tissue between the white of the eye and retina (at the back of the eye). It is part of the uvea and supplies nutrients to the inner parts of the eye. Inflammation of the choroid is called choroiditis.
What is choroid plexus in simple words? ›A network of blood vessels and cells in the ventricles (fluid-filled spaces) of the brain. The blood vessels are covered by a thin layer of cells that make cerebrospinal fluid.
What is the choroid plexus of the eye? ›The choroid, also known as the choroidea or choroid coat, is a part of the uvea, the vascular layer of the eye, and contains connective tissues, and lies between the retina and the sclera. The human choroid is thickest at the far extreme rear of the eye (at 0.2 mm), while in the outlying areas it narrows to 0.1 mm.
Does the choroid protect the eye? ›
This thin layer of tissue is made up almost entirely of blood vessels. These blood vessels supply oxygen and nutrients to the outer part of the retina. In short, the choroid is the life source that keeps the retina healthy and functioning.
How does the choroid nourish the eye? ›1 It contains the retinal pigmented epithelial cells and provides oxygen and nourishment to the outer retina. The choroid forms the uveal tract, which includes the iris and the ciliary body. The dark-colored melanin pigment in the choroid absorbs light and limits reflections within the eye that could degrade vision.
What are the parts of choroid plexus? ›The choroid plexus consists of a layer of cuboidal epithelial cells surrounding a core of capillaries and loose connective tissue. The epithelium of the choroid plexus is continuous with the ependymal cell layer (ventricular layer) that lines the ventricular system.
What structures make up the choroid plexus? ›The choroid plexus is composed of blood vessels and specialized epithelial tissue called ependyma. Ependymal cells contain hair-like projections called cilia which form a tissue layer that encases the choroid plexus. Ependymal cells also line the cerebral ventricles and spinal cord central canal.
What do parts of the choroid form? ›The choroid forms part of the vascular layer of the eyeball, along with the ciliary body and iris. It is a thin, pigmented vascular connective tissue layer of the eyeball that extends from the ora serrata to the optic nerve (CN II).
What is the blood supply to the choroid? ›Blood is delivered to the choroid through the ophthalmic artery that branches to form (typically) two posterior ciliary arteries, 35 which in turn branch to form many short posterior ciliary arteries and two long posterior ciliary arteries.
What disease affects the choroid of the eye? ›Choroidal dystrophy is an eye disorder that involves a layer of blood vessels called the choroid. These vessels are between the sclera and retina. In most cases, choroidal dystrophy is due to an abnormal gene, which is passed down through families.
What nerve Innervates the choroid in eye? ›The choroid is richly innervated by parasympathetic, sympathetic and trigeminal sensory nerve fibers that regulate choroidal blood flow in birds and mammals, and presumably other vertebrate classes as well.