Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma.

Arachnoid granulations (AG) are poorly investigated. Historical reports suggest that they regulate brain volume by passively transporting cerebrospinal fluid (CSF) into dural venous sinuses. Here, we studied the microstructure of cerebral AG in humans with the aim of understanding their roles in physiology. We discovered marked variations in AG size, lobation, location, content, and degree of surface encapsulation. High-resolution microscopy shows that AG consist of outer capsule and inner stromal core regions. The fine and porous framework suggests uncharacterized functions of AG in mechanical CSF filtration. Moreover, internal cytokine and immune cell enrichment imply unexplored neuroimmune properties of these structures that localize to the brain-meningeal lymphatic interface. Dramatic age-associated changes in AG structure are additionally identified. This study depicts for the first time microscopic networks of internal channels that communicate with perisinus spaces, suggesting that AG subserve important functions as transarachnoidal flow passageways. These data raise new theories regarding glymphatic-lymphatic coupling and mechanisms of CSF antigen clearance, homeostasis, and diseases.

Identification of lymphatic endothelium in cranial arachnoid granulation-like dural gap.

The dynamics of cerebrospinal fluid (CSF) are essential for maintaining homeostasis in the central nervous system. Despite insufficiently detailed descriptions of their structural and molecular properties for a century, cranial arachnoid granulations (CAGs) on meninges have been thought to participate in draining CSF from the subarachnoid space into the dural sinuses. However, recent studies have demonstrated the existence of other types of CSF drainage systems, such as lymphatic vessels adjacent to dural sinus and paravascular space in the brain so-called glymphatic system. Therefore, the role of CAGs in CSF drainage has become dubious. To better understand CAG function, we analyzed the ultrastructure and molecular identity of CAG-like structure on meninges adjacent to the superior sagittal sinus of pigs. Transmission electron microscopy analysis revealed that this structure has a reticular conglomerate consisting of endothelial cells that resembles lymphatic linings. Furthermore, immunohistochemistry and immunoelectron microscopy showed that they express molecules specific to lymphatic endothelial cell. We coined a name 'CAG-like dural gap (CAG-LDG)' to this structure and discussed the physiological relevance in terms of CSF drainage.

Ultrastructural and Molecular Characterization of Platelet-derived growth factor Beta-Positive Leptomeningeal Cells in the Adult Rat Brain.

The leptomeninges, referring to the arachnoid and pia mater and their projections into the perivascular compartments in the central nervous system, actively participate in diverse biological processes including fluid homeostasis, immune cell infiltrations, and neurogenesis, yet their detailed cellular and molecular identities remain elusive. This study aimed to characterize platelet-derived growth factor beta (PDGFR-ß)-expressing cells in the leptomeninges in the adult rat brain using light and electron microscopy. PDGFR-ß+ cells were observed in the inner arachnoid, arachnoid trabeculae, pia mater, and leptomeningeal sheath of the subarachnoid vessels, thereby forming a cellular network throughout the leptomeninges. Leptomeningeal PDGFR-ß+ cells were commonly characterized by large euchromatic nuclei, thin branching processes forming web-like network, and the expression of the intermediate filaments nestin and vimentin. These cells were typical of active fibroblasts with a well-developed rough endoplasmic reticulum and close spatial correlation with collagen fibrils. Leptomeningeal PDGFR-ß+ cells ensheathing the vasculature in the subarachnoid space joined with pial PDGFR-ß+ cells upon entering the cortical parenchyma, yet perivascular PDGFR-ß+ cells in these penetrating vessels underwent abrupt changes in their morphological and molecular characteristics: they became more flattened with loss of immunoreactivity for nestin and vimentin and deficient collagen deposition, which was indicative of inactive fibroblasts termed fibrocytes. In the cortical parenchyma, PDGFR-ß immunoreactivity was almost exclusively localized to larger caliber vessels, and significantly decreased in capillary-like microvessels. Collectively, our data identify PDGFR-ß as a novel cellular marker for leptomeningeal fibroblasts comprising the leptomeninges and perivascular adventitial cells of the subarachnoid and penetrating large-sized cortical vasculatures.

Ultrastructural changes in the Liliequist membrane in the hydrocephalic process and its implications for the endoscopic third ventriculostomy procedure.

AIM: Fenestration of Liliequist membrane (LM) during endoscopic third ventriculostomy (ETV) is extremely important for the success of the procedure. It is noteworthy that LM usually shows a tough and dense stucture in long-standing hydrocephalus cases different from its usual arachnoidal membrane-like structure observed in new-onset hydrocephalus cases. The structural variation of LM in different hydrocephalic states was investigated histologically in this study. MATERIAL AND METHODS: Specimens of LM obtained during endoscopic fenestration in 11 cases were examined under transmission-electron-microscopy. Six cases had long-standing hydrocephalus and five had new-onset triventricular hydrocephalus. None of the cases had a history of infection or hemorrhage. RESULTS: In cases with long-standing hydrocephalus, ultrastructural examinations revealed the existence of regular and dense bundles of type-I collagen among the fibroblast-like cells, which were closely connected by dense desmosomes and gap-junctions. In cases with new-onset hydrocephalus, it was observed that the cells usually had long cytoplasmic extentions and were connected with loose desmosomes. Sparse type-I collagen bundles were observed rarely among the cells. CONCLUSION: These results suggest that the structure of LM may change with the duration of the hydrocephalic process. This may help explain the tough and dense LM stucture observed during the ETV procedure in cases with long-standing-hydrocephalus.

Arachnoid cells on culture plates and collagen scaffolds: phenotype and transport properties.

INTRODUCTION: The arachnoid tissue is a critical component of cerebrospinal fluid removal. Failure of that function results in hydrocephalus, a serious medical condition. The purpose of this study was to characterize arachnoid cell transport in culture and on three-dimensional collagen scaffold. METHODS: Arachnoid cells were harvested from rat brainstems and cultured onto bilayered bovine collagen scaffolds. Cell growth and phenotype (protein expression and morphometry) were determined. Permeability and hydraulic conductivity were quantified. RESULTS: Cells harvested from the anterior brainstem surface exhibited arachnoid cell phenotype (positive for vimentin, desmoplakin, and cytokeratin), readily penetrated the collagen scaffold, and doubled approximately every 2-3 days. The transepithelial electrical resistance value for a monolayer of cells was 160 Ω cm(2) and the permeability of indigo carmine was 6.7×10(-6)±1.1×10(-6) cm/s. Hydraulic conductivity of the collagen construct was 6.39 mL/min/mmHg/cm(2). CONCLUSION: Cells isolated from the anterior brain stem exhibited the same phenotype as those found in the native tissue and exhibited aspects of barrier function found in vivo. These studies suggest that an ex vivo model for the arachnoid granulation can be developed.

[Structure of the arachnoid layer of the human spinal meninges: a barrier that regulates dural sac permeability]. / Morfología de la lámina aracnoidea espinal humana. Barrera que limita la permeabilidad del saco dural.

OBJECTIVES: Drugs injected into the epidural space are known to penetrate the subarachnoid space by simple diffusion through the dural sac. We aimed to study the cellular ultrastructure of the arachnoid membrane and the type of intercellular junctions responsible for creating the barrier that regulates the passage of drugs through the dural sac in humans. MATERIAL AND METHODS: Fourteen tissue samples of arachnoid membrane were taken from 2 patients during procedures that required opening the lumbar dural sac. The samples were treated with glutaraldehyde, osmium tetroxide, ferrocyanide and acetone, and then embedded in resin. Ultrathin sections were stained with lead citrate for examination by transmission electron microscopy. RESULTS: The arachnoid membrane was 35 to 40 microm thick. The outer surface contained neurothelial cells (dural border cells) along the subdural compartment, while the internal portion was made up of a plane 5 to 8 microm thick with 4 to 5 arachnoid cells overlapping to form a barrier layer. The intercellular spaces on this plane were 0.02 to 0.03 microm wide; the arachnoid cells were bridged by specialized junctions (desmosomes and other tight junctions). CONCLUSIONS: Structural features of the arachnoid cells provide a barrier within the human dural sac. They occupy only the internal portion of the arachnoid membrane. Specialized intercellular junctions explain the selective permeability of this membrane.

Morfología de la lámina aracnoidea espinal humana. Barrera que limita la permeabilidad del saco dural / Structure of the arachnoid layer of the human spinal meninges: a barrier that regulates dural sac permeability

OBJETIVOS: Se ha demostrado que las moléculas inyectadas en el espacio epidural pasan desde éste al espacio subaracnoideo por difusión simple a través de la pared del saco dural. Nuestro objetivo fue estudiar la ultraestructura de células de la lámina aracnoidea y tipo de uniones especializadas responsables del efecto barrera que gobierna el tránsito de moléculas a través del saco dural humano. MATERIAL Y MÉTODO: Se estudiaron catorce muestras de la lámina aracnoidea obtenidas de dos pacientes durante intervenciones con apertura del saco dural lumbar. Las muestras se trataron con glutaraldehido, tetróxido de osmio, ferrocianuro, acetona, e incluyeron en resina. Los cortes ultrafinos se contrastaron con citrato de plomo, para poder ser observados con un microscopio electrónico de transmisión. RESULTADOS: La lámina aracnoidea posee un espesor de 35-40 μm. En su porción externa se hallan células neuroteliales del compartimento subdural, mientras que su porción interna está formada por un plano celular de 5-8 μm de espesor, constituido por la superposición de 4-5 células aracnoideas que forman la capa barrera. El espacio intercelular de este plano fue de 0,02-0,03 μm. Entre las células aracnoideas se encontraron uniones especializadas de membrana de tipo desmosomas y uniones estrechas. CONCLUSIONES: Las células aracnoideas poseen características estructurales que aseguran la función barrera del saco dural humano y no ocupan todo el espesor de la lámina aracnoidea, sólo su porción interna. La presencia de uniones especializadas de membrana entre sus células justifica la permeabilidad selectiva de esta lámina(AU)

OBJETIVES: Drugs injected into the epidural space are known to penetrate the subarachnoid space by simple diffusion through the dural sac. We aimed to study the cellular ultrastructure of the arachnoid membrane and the type of intercellular junctions responsible for creating the barrier that regulates the passage of drugs through the dural sac in humans. MATERIAL AND METHODS: Fourteen tissue samples of arachnoid membrane were taken from 2 patients during procedures that required opening the lumbar dural sac. The samples were treated with glutaraldehyde, osmium tetroxide, ferrocyanide and acetone, and then embedded in resin. Ultrathin sections were stained with lead citrate for examination by transmission electron microscopy. RESULTS: The arachnoid membrane was 35 to 40 μm thick. The outer surface contained neurothelial cells (dural border cells) along the subdural compartment, while the internal portion was made up of a plane 5 to 8 μm thick with 4 to 5 arachnoid cells overlapping to form a barrier layer. The intercellular spaces on this plane were 0.02 to 0.03 μm wide; the arachnoid cells were bridged by specialized junctions (desmosomes and other tight junctions). CONCLUSIONS: Structural features of the arachnoid cells provide a barrier within the human dural sac. They occupy only the internal portion of the arachnoid membrane. Specialized intercellular junctions explain the selective permeability of this membrane(AU)

Ex vivo model of cerebrospinal fluid outflow across human arachnoid granulations.

PURPOSE: The brain's arachnoid membrane with granulations is an important biological barrier whose responsibilities include the transmission of cerebrospinal fluid (CSF) and the regulation of pressure. Membrane disturbance may cause changes that are difficult to replicate with animal models, suggesting the need for a model using human arachnoid membrane with granulations for the study of conditions such as Alzheimer disease, hydrocephalus, and pseudotumor cerebri. The authors detail the development and validation of an ex vivo model of CSF outflow across human arachnoid granulations (AGs) as an approximation of in vivo conditions. METHODS: Human AGs were perfused at normal physiological pressure in physiological and nonphysiological directions for permeability data. Fluorescent particle perfusion with electron microscopy identified outflow pathways through the AGs. RESULTS: This human ex vivo model demonstrated in vivo properties of unidirectionality, particle transport, and ultrastructure, similar to our 2005 in vitro model. The average baseline hydraulic conductivity in the physiological direction (n = 20) was 1.05 +/- 0.15 microL/min/mm Hg/cm(2) compared with 0.11 +/- 0.03 microL/min/mm Hg/cm(2) in the nonphysiological direction (n = 3) under statistically equivalent (P = 0.46) average normal physiological pressures (5.88 +/- 0.22 mm Hg and 6.14 +/- 0.23 mm Hg, respectively). CONCLUSIONS: The ex vivo model is feasible and herein demonstrated. These findings agree with in vivo CSF outflow. This model increases understanding of the clearance not only of CSF but also of metabolites through the arachnoid membrane. Additional evidence suggests, but does not yet prove, that CSF outflow may occur in a similar manner in the arachnoid membrane adjacent to the granulations, in addition to the flow through the AGs. This is a topic for further investigation.

Aracnoides trabecular, piamadre espinal humana y anestesia subaracnoidea / Trabecular arachnoid membrane, human spinal piamater and subarachnoid anesthesia

En los textos de anestesiología se aportan pocos detalles sobre la aracnoides trabecular y la piamadre espinal humana, a pesar de ser estructuras íntimamente relacionadas con los anestésicos locales administrados en una anestesia subaracnoidea. Complicaciones tales como el síndrome de cauda equina y el síndrome de irritación radicular transitorio posterior a la realización de bloqueos subaracnoideos, sumado a la alta permeabilidad que ha sido asociada con la piamadre, nos ha motivado a investigar sobre la ultraestructura de estas meninges. Método. Las muestras estudiadas se tomaron de cadáveres recientes y fueron examinadas por microscopía electrónica de transmisión y de barrido. Resultados. El trabeculado aracnoideo rodeaba a las raíces nerviosas, a la médula y a los vasos que se encontraban dentro del espacio subaracnoideo, limitando zonas. La piamadre estaba formada por un plano celular y por un compartimiento subpial. En el plano celular existían perforaciones naturales, especialmente en la región del cono medular y en las raíces nerviosas. Conclusiones. La inyección accidental de anestésicos locales dentro de las fundas que formaban el trabeculado aracnoideo podría justificar una dilución inadecuada de estas soluciones y el origen de síndromes neurotóxicos transitorios o permanentes. La alta permeabilidad de la piamadre podría deberse, en parte, a la existencia de perforaciones naturales, las cuales facilitarían un pasaje rápido de las sustancias introducidas en el líquido cefalorraquídeo hacia las raíces nerviosas y la médula espinal. En este caso, la membrana basal ubicada por debajo de las fibras colágenas del compartimiento subpial sería la única estructura limitante previa al tejido glio-neuronal de la médula.

Few details are to be found in anesthesiology texts concerning the trabecular arachnoid membrane and the human spinal pia mater in spite of being structures that are intimately related to local anesthetics administered in subarachnoid anesthesia. We were driven to investigate the ultrastructure of these meninges by complications such as the cauda equina syndrome and the transitory radicular irritation syndrome following subarachnoid blocks, added to the high permeability associated to the pia mater. Method. The samples analyzed were taken from recently deceased cadavers and were examined under transmission and scanning electron microscopy. Results. The arachnoid trabeculation surrounded the nerve roots, the spinal cord and the vessels within the subarachnoid space, limiting areas. The pia mater was formed by a cellular plane and by a sub-pial compartment. There were natural perforations in the cellular plane, particularly in the medullar cone region and the nerve roots. Conclusions. Accidental injection of local anesthetics into the sheaths formed by arachnoid trabeculation could be the cause of inadequate dilution of these solutions and the source of transitory or permanent neurotoxic syndromes. The high permeability of the pia mater could be partly due to the existence of natural perforations, which enable the quick passage of the substances introduced in the cerebrospinal fluid into the nerve roots and spinal cord. ln this case, the basal membrane located underneath the collagen fibers of the subpial compartment would be the only limiting structure before the glioneural tissue of the spinal cord.

Os textos de anestesiologia fornecem poucos detalhes sobre a aracnóide trabecular e a pia-máter espinhal humana, apesar delas serem estruturas intimamente relacionadas com os anestésicos locais administrados em uma anestesia subaracnóidea. Complicações tais como a síndrome de cauda eqüina e a síndrome de irritação radicular transitória posterior a bloqueios subaracnóideosas quais se soma a alta permeabilidade, que tem sido associada à pia-máter -levou-nos a pesquisar a ultraestrutura dessas meninges. Método. As amostras estudadas foram coletadas de cadáveres recentes e examinadas por microscopia eletrónica de transmissão e de varredura. Resultados. A trabeculação aracnóidea rodea va as raízes nervosas, a medula e os vasos no interior do espaço subaracnóide, limitando zonas. A pia-máter estava formada por um plano celular e um espaço subpial. No plano celular existiam perfurações naturais, especialmente na regiáo do cone medular e nas raízes nervosas. Conclusóes. A injeção acidental de anestésicos locais no interior das coberturas que formavam a trabeculação aracnoidea poderia justificar uma diluição inadequada das soluções e a origem de síndromes neurotóxicas transitórias ou permanentes. A causa da alta permeabilidade da pia-máter seria, em parte, a existencia de perfurações naturais que facilitariam a rápida passagem das substancias introduzidas no líquido cefalorraquiano para as raizes nervosas e a medula espinhal. Neste caso, a membrana basal localizada abaixo das fibras colágenas do espaço subpial seria a única estrutura limitante anterior ao tecido glio-neuronal da medula.

Cefalea pospunción dural. Ultraestructura de las lesiones durales y agujas espinales usadas en las punciones lumbares / Post dural puncture cephalea. UItra-structure of the dural lesions and spinal needles used in lumbar punctures

Con el microscopio electrónico de barrido, se examinó la morfología de las lesiones durales y aracnoideas en muestras de saco dura-aracnoideo extraídos de cuerpos humanos recién fallecidos. Después de hacer punciones con agujas Quincke y Whitacre 22-G y 25-G, no se encontraron diferencias estadísticamente significativas entre las áreas de las lesiones durales y aracnoideas. La lesión tenía una morfología diferente con cada aguja. La aguja Whitacre producía una lesión de bordes rotos con gran destrucción de fibras durales, mientras que la aguja "biselada" Quincke causaba una lesión con forma de "U" o "V", como la tapa de una lata, con bordes de corte limpio. La alineación paralela o perpendicular entre el bisel de la punta de la aguja Quincke y el eje del axis no modificaba el área de las lesiones durales y aracnoideas. Se analizó cómo se puede producir cada tipo de lesión y se interpretaron los otros factores que podrían participar. Con la misma técnica se estudiaron agujas espinales nuevas obteniéndose, en cierto porcentaje de éstas, una imagen tridimensional a gran aumento de la fragmentación de puntas, defectos del pulido y existencia de rebabas. Se analizó cómo se pueden alterar las puntas de las agujas al chocar contra el hueso y de qué manera los defectos de estas constituyen otro aspecto de la compleja suma de variables que predisponen a la aparición de una cefalea pospunción dural.

The morphology of dural and arachnoid lesions was electronically scanned, from samples of dura-arachnoid sacs taken from recently deceased human beings. After punctures with Quincke y Whitacre 22-G y 25-G needles, no statistically significant differences were found between the areas of the dural and arachnoid lesions. The lesion had a different morphology with each needle. The Whitacre needle produced a lesion of broken edges with great destruction of the dural fibers, whereas the Quincke "beveled" needle caused a "U" or "V" shaped lesion, like the lid of a can, with clean-cut edges. The parallel or perpendicular alignment between the bevel of the Quincke needle tip and the axis of the axis did not modify the area of the dural and arachnoid lesions. A study was made of how each type of lesion could have come about and of other possible participating factors. The same technique was used to study new spinal needles and, in a certain percentage, a three dimensional image was obtained, showing a great increase in the fragmentation of the tips, burnish defects and the existence of burrs. We also analyzed how hitting against the bone could affect the tips of the needles and how their defects could be another factor in the complex sum of variables that predispose the patient to suffer post dural puncture cephalea.

Com o microscópio eletrônico de varredura, examinou-se a morfologia das lesoes durais e da aracnóide em amostras de saco dural-aracnóideo extraídos de corpos humanos de recem-falecidos. As diferencas entre as áreas das lesoes durais e da aracnóide pós-puncao com agulhas Quincke e Whitacre 22-G e 25-G nao foram estatisticamente significativas, e a morfologia da lesao causada com cada agulha foi diferente. A agulha Whitacre provocou lesao de bordas rompidas com grande destruicao de fibras durais, enquanto a agulha "biselada" Quincke causou lesao com forma de "U" ou "V", como a tampa de uma lata, com bordas de corte limpo. O alinhamento paralelo ou perpendicular do bisel da ponta da agulha Quincke com o eixo do áxis nao modificou a área das lesóes durais e da aracnóide. Foram analisadas as causas de cada tipo de lesao e interpretados outros fatores envolvidos. Utilizando a mesma técnica, avaliaram-se imagens tridimensionais de algumas agulhas espinhais novas tiradas com grande aumento: fragmentacao das pontas, defeitos de polimento e presenca de rebarbas. Avaliou-se também como se modificam as pontas das agulhas ao atingirem o osso e a influência dos defeitos das pontas na complexa soma de variáveis que predispoem o aparecimento de cefaléia pós-puncao dural.

An experimental Staphylococcus aureus meningitis model for investigating induced leptomeningeal and subpial inflammation in rats: a transmission electron microscopy study.

OBJECTIVE: To evaluate leptomeningeal and subpial inflammatory responses of experimental Staphylococcus aureus bacteriemia following intraperitoneal and intravenous applications and to compare the inflammatory reactions in different regions of central nervous system. MATERIAL AND METHODS: Forty anesthetized rats were divided into four groups equal in number. The rats in group-I were given 1 ml suspension of Staphylococcus aureus intraperitoneally. Group-II was the control group of group I; it was administrated 1 ml 0.9% NaCl in water intraperitoneally. The rats in group-III were given the same amount of bacteria intravenously. Group IV was the control group of the group-III; it was administrated 1 ml 0.9% NaCl solution intravenously. The rats were sacrificed on the 21st day. Inflammatory changes of different regions of the central nervous system were examined under transmission electron microscopy. Statistical analysis was done by using variance analysis, Bonferroni, Tamhane post hoc, Student's t and univariate tests. RESULTS: Thoracic and occipital regions were the most vulnerable zones. Increasing of collagen tissue was the most detected inflammatory change. CONCLUSION: This experimental model can be used for inducing subpial and leptomeningeal inflammations and it may be developed for investigations of pathogenesis of leptomeningitis during systemic infections.

Human spinal arachnoid villi revisited: immunohistological study and review of the literature.

OBJECT: Few have described the relationship between arachnoid protrusions (villi) and adjacent spinal radicular veins, and the descriptions that do exist are conflicting. Some authors have even denied the presence of spinal arachnoid villi, suggesting that they play no role in cerebrospinal fluid (CSF) absorption. METHODS: To further elucidate these structures, laminectomies from C-2 inferiorly to S-2 were performed in 10 fresh human adult cadavers. Following removal of the laminae, the dural nerve sleeves were identified and the spinal nerves excised 1 cm lateral and medial to the intervertebral foramina. Samples were submitted for histological and immunohistological analysis. RESULTS: The authors identified arachnoid villi in all specimens. The length of these structures was approximately 50 to 170 microm. Regionally, these villi were more concentrated in the lumbar region, but they were not present at every vertebral level, with observed skip zones. Occasionally, more than one villus was identified per vertebral level. The majority of villi were intimately related to an adjacent radicular vein. There was a direct relationship between the size of the adjacent radicular vein, and the presence and number of arachnoid villi. CONCLUSIONS: Findings in the present study have demonstrated that arachnoid villi exist and are morphologically associated with radicular veins. These data support the theory that CSF absorption occurs not only intracranially but also along the spinal axis. Further animal studies are necessary to prove that CSF traverses these villi and is absorbed into the spinal venous system.

Microscopic anatomy of the brain-meningioma interface.

We analyzed the relation between meningioma and the brain in 50 surgical cases. So-called capsule formation was seen in 20 meningiomas, of which 13 were categorized as thin and 7 as thick. In 21 meningiomas the arachnoid membrane was intact, and 10 meningiomas had no underlying arachnoid membrane. The other 19 tumors showed partial disruption of the arachnoid membrane. The degree of arachnoid disruption correlated with the tumor grade, perifocal edema, pial blood supply on angiography, and tumor size. The existence of brain invasion correlated with the tumor grade and partially with tumor size. In case of invasive tumor, GFAP-positive cells were found deep in the tumor, usually in contact with blood vessels. The axons in gliotic brain often showed degenerative changes such as ballooning or varicose swelling. Meningiomas were usually demarcated by a basement membrane that was collagen type 4 (Col4)-positive. However, atypical and anaplastic meningiomas usually lacked Col4 staining at the interface. In two benign meningiomas that looked like an invasive growth, Col4 staining was seen above the brain. A pia mater-like structure covered the tumor surface in both cases. We could not demonstrate a relation between the expression of matrix metalloproteinase (MMP)-2 or MMP-9 and arachnoid disruption or brain invasion.

Obstructive hydrocephalus associated with arachnoid cyst in the elderly.

We present a case of a symptomatic frontal arachnoid cyst associated with hydrocephalus in an elderly patient. It is well known that symptomatic arachnoid cysts usually develop at an early age. This condition is rarely observed in the elderly. The authors hypothesized that compression of the brain and obstructive hydrocephalus caused the arachnoid cyst to become symptomatic.

Spatial learning transiently disturbed by intraventricular administration of ouabain.

The presence of sodium-potassium-adenosine triphosphatase (Na+,K+-ATPase) on the surface of arachnoid cells indicates that active transport of electrolytes and water occurs there. Previously, we accidentally found that intraventricular administration of TGF-beta1 impaired rat spatial learning. Levels of Na+,K+ -ATPase were decreased in arachnoid cells with fibrosis. To characterize the role of the Na+,K+ -ATPase, Wistar rats were intraventricularly administered a total of 200 microl of ouabain, at concentrations of 10(-5), 10(-4) and 10(-3) M, for one week with an osmotic pump, and were examined with a Morris water maze. Latency for reaching the platform did not significantly differ between ouabain-administered rats and controls. Spatial learning was impaired in a dose-dependent manner. Na+,K+ -ATPase activity of arachnoid cells ceased during ouabain administration, and recovered completely three weeks after the end of ouabain administration. The present results suggest that the Na+,K+ -ATPase on the surface of arachnoid cells contributes to maintenance of rat spatial learning.

Tridimensional architecture of the collagen element in the arachnoid granulations in humans: a study on scanning electron microscopy.

The arachnoid granulations of adult individual of both sexes were studied through scanning electron microscopy. The dura mater and arachnoid meninges of individuals were collected at the Service of Death Verification of São Paulo - USP and fixed in Karnovsky solution. After this period the material was prepared for analysis in electron microscope. Our results demonstrated that the arachnoid granulations are formed by a pedicle, body and apex, being surrounded by a capsule of connective tissue, which in turn is composed of, basically, bundles of collagen fibers that line pores of different shapes and sizes. The smaller pores are lined by tiny bundles and are located at the apical region of the granulation and the larger are lined by thicker bundles and are located at the lateral regions. In the body we verified that the bundles of collagen fibers compose a fibrous meshwork and in some regions these bundles have circular orientation, forming pores similar to those found at the region of the capsule.

Macrophages and dendritic cells in the rat meninges and choroid plexus: three-dimensional localisation by environmental scanning electron microscopy and confocal microscopy.

The present investigation provides novel information on the topographical distribution of macrophages and dendritic cells (DCs) in normal meninges and choroid plexus of the rat central nervous system (CNS). Whole-mounts of meninges and choroid plexus of Lewis rats were incubated with various anti-leucocyte monoclonal antibodies and either visualised with gold-conjugated secondary antibody followed by silver enhancement and subsequent examination by environmental scanning electron microscopy or by the use of fluorochromes and confocal microscopy. Large numbers of MHC class II(+) putative DCs were identified on the internal or subarachnoid aspect of dural whole-mounts, on the surface of the cortex (pia/arachnoid) and on the surface of the choroid plexus. Occupation of these sites would allow DCs access to cerebrospinal fluid (CSF) and therefore allow antigens into the subarachnoid space and ventricles. By contrast, macrophages were less evident at sites exposed to CSF and were more frequently located within the connective tissue of the dura/arachnoid and choroid plexus stroma and also in a sub-pial location. The present data suggest that DC may be strategically located within the CNS to sample CSF-borne antigens. Furthermore, the data suggest that CNS tissue samples collected without careful removal of the meninges may inadvertently be contaminated by DCs and meningeal macrophages.

Molecular characterization of desmosomes in meningiomas and arachnoidal tissue.

Intercellular junctions morphologically identical to epithelial desmosomes are known structures in meningiomas and arachnoidal tissue. Desmoplakin as one of the desmosomal plaque components has proven to be a reliable marker for diagnosis of meningeal tumors. Here we demonstrate by immunofluorescence microscopy, immunoblot and reverse transcription-PCR reactions that cells of arachnoidal tissue, of diverse meningioma subtypes and of a meningioma-derived cell line contain the full complement of the typical desmosomal proteins desmoplakin (DP), plakophilin 2 (PP2), desmocollin 2 (Dsc2) and desmoglein 2 (Dsg2). Consequently, all these molecules are suitable for diagnostic applications of meningioma tumors. In addition to these constitutive desmosomal components, representative for single-layered (simple) epithelia, the dural border cells of the arachnoid and about 60% of the meningiomas tested were positive for desmocollin 3 (Dsc3), a protein in epithelia taken as an indicator for differentiation.

Architecture of arachnoid trabeculae, pillars, and septa in the subarachnoid space of the human optic nerve: anatomy and clinical considerations.

AIMS: To describe the anatomy and the arrangement of the arachnoid trabeculae, pillars, and septa in the subarachnoid space of the human optic nerve and to consider their possible clinical relevance for cerebrospinal fluid dynamics and fluid pressure in the subarachnoid space of the human optic nerve. METHODS: Postmortem study with a total of 12 optic nerves harvested from nine subjects without ocular disease. All optic nerves used in this study were obtained no later than 7 hours after death, following qualified consent for necropsy. The study was performed with transmission (TEM) and scanning electron microscopy (SEM). RESULTS: The subarachnoid space of the human optic nerve contains a variety of trabeculae, septa, and stout pillars that are arranged between the arachnoid and the pia layers of the meninges of the nerve. They display a considerable numeric and structural variability depending on their location within the different portions of the optic nerve. In the bulbar segment (ampulla), adjacent to the globe, a dense and highly ramified meshwork of delicate trabeculae is arranged in a reticular fashion. Between the arachnoid trabeculae, interconnecting velum-like processes are observed. In the mid-orbital segment of the orbital portion, the subarachnoid space is subdivided, and can appear even loosely chambered by broad trabeculae and velum-like septa at some locations. In the intracanalicular segment additionally, few stout pillars and single round trabeculae are observed. CONCLUSION: The subarachnoid space of the human optic nerve is not a homogeneous and anatomically empty chamber filled with cerebrospinal fluid, but it contains a complex system of arachnoid trabeculae and septa that divide the subarachnoid space. The trabeculae, septa, and pillars, as well as their arrangement described in this study, may have a role in the cerebrospinal fluid dynamics between the subarachnoid space of the optic nerve and the chiasmal cistern and may contribute to the understanding of the pathophysiology of asymmetric and unilateral papilloedema. All the structures described are of such delicate character that they can not even be visualised with high resolution magnetic resonance imaging (MRI).