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Adhesion of Porphyromonas gingivalis to cultured pocket epithelium: mono- and multi-layered.

Adhesion of bacteria to epithelial cells might be influenced by the degree of cell differentiation, as observed in the multi-layering process of epithelial cells. In the present study, the adhesion of a large group of clinical Porphyromonas gingivalis strains (n=11) to in vitro cultured mono- and multi-layers of epithelial cells was examined and compared. The tissue samples originated from 6 patients with chronic adult periodontitis. Porphyromonas gingivalis bacteria adhered more to mono-layers as opposed to the more differentiated multi-layers. Differences between the clinical P. gingivalis strains, however, became obvious only on multi-layers. These partially differentiated cells may also better represent the individual subject variations. Mono-layer cultures, which are simpler to obtain, seem to be less precise. The importance of cell differentiation on bacterial adhesion needs more attention.

Adult↗

Region-dependent role of the mucous/glycocalyx layers in insulin permeation across rat small intestinal membrane.

The regional difference in the contribution of the mucous/glycocalyx layers in rat small intestine, as a diffusional or enzymatic barrier, to the absorption of insulin was investigated by in vitro studies. The mucous/glycocalyx layers from the duodenum, the jejunum, and the ileum in rat were successfully removed without damaging membrane integrity, by exposing them to a hyaluronidase solution in situ. In an in vitro transport experiment, the apparent permeability coefficient (P(app)) of insulin for the hyaluronidase-pretreated group was significantly increased compared to the PBS-pretreated (control) group in all small intestinal regions, and the P(app) of insulin in both PBS- and hyaluronidase-pretreated groups increased in the following order: duodenum < jejunum < ileum. On the other hand, irrespective of small intestinal regions, the P(app) of FD-4 and of antipyrine, respectively the passive para- and transcellular permeation marker, exhibited no significant differences between PBS- and hyaluronidase-pretreated group. In addition, a significant amount of insulin was degraded in the mucous/glycocalyx layers compartment removed by hyaluronidase pretreatment, and the degradation activity in the mucous/glycocalyx layers showed regional differences in the following order: duodenum > jejunum > ileum. These findings suggest that, irrespective of small intestinal regions, the mucous/glycocalyx layers contributed to insulin permeation predominantly as an enzymatic barrier, and not as a diffusional barrier. Furthermore, the variation of the enzymatic activities in the mucous/glycocalyx layers and in the brush-border membrane would be one factor that accounts for the regional differences in the transport of insulin.

Animals↗

Histopathologic correlation of the three-layered intravascular ultrasound appearance of normal adult human muscular arteries.

The purpose of this study was to correlate intravascular ultrasound images from normal peripheral muscular arteries with the microscopic arterial components by using surgical microdissection techniques. There has been uncertainty about the precise anatomic constituents that are represented by the intravascular ultrasound three-layer image in human peripheral arteries. Forty of 66 grossly normal human femoropopliteal arterial segments obtained at autopsy were found to have a three-layered appearance and were subjected to selective surgical microdissection of intima, media, or adventitia. After microdissection, arteries were imaged with a 30 MHz intravascular ultrasound system; two observers blindly reviewed video tapes to assess for the presence or absence of a one-, two-, or three-layered arterial appearance. Removal of internal elastic lamina and/or intima results in a weak but evident inner ultrasound acoustic interface as a result of the media, which is normally echo-lucent. Removal of the adventitia and/or external elastic lamina results in a weak outer ultrasound acoustic interface. Isolated removal of the media does not alter the three-layered ultrasound image. In normal adult human femoropopliteal arteries the inner bright acoustic reflection (layer) is derived from the interface of blood with the intima and internal elastic lamina and the second bright interface (third layer) is from the external elastic lamina and adventitia. The mid-echo-lucent zone is the result of the media. However, any portion of the arterial wall, including muscular media, can act as an acoustic interface.

Adult↗

Protein-protein interactions and structural entities within the sea urchin extraembryonic matrix, the hyaline layer.

We have investigated the effects of a variety of experimental conditions on the structural integrity of the sea urchin extraembryonic matrix, the hyaline layer. Removal of Ca2+ resulted in the quantitative release of hyalin from isolated layers. Protein gel blot analyses indicated that, in the absence of Ca2+, hyalin was also quantitatively released from the layers surrounding 1-h-old embryos. However, no other polypeptides of the hyaline layer were released in significant amounts. The layers remaining after removal of hyalin were refractory to digestion with proteinase K and dissociated only in the presence of chaotropes. These results provide insights into the structural organization within the hyaline layer as well as the role of the embryonic cell surface in maintaining the structural integrity of this extraembryonic matrix.

Animals↗

X-ray diffraction and thermal studies of crystals from the outer and inner layers of human dental enamel.

X-ray diffraction showed that crystals from the outer layer had larger crystallite sizes, a-axis length and peak intensities than the inner layer crystals. Upon heating, apatites in both layers showed a contraction of a-axis length and changed their crystallite sizes along the direction of the a-axis independently of changes along the c-axis. The contraction of the a-axis length is attributed to loss of structurally incorporated water from the apatite lattice, causing void formation along the c-axis and altering the crystallite size normal to the c-axis. Whitlockite was detected in samples from both layers at temperatures above 800 degrees C, and the temperature required for whitlockite formation was considered to be influenced by the experimental atmosphere. The peak shift of whitlockite with temperature indicates that the whitlockite initially formed was magnesium rich. As to the amount of structurally incorporated water in both layers' apatites, the a-axis contraction data were inconsistent with the a-axis length data. This inconsistency indicates a larger degree of magnesium substitution in the inner layer apatite. A larger degree of magnesium substitution in apatite would show a smaller crystallite size, a weaker apatite peak intensity and a larger amount of whitlockite formation.

Apatites↗

Correction of the apparent Michaelis constant, biased by an unstirred layer, if a passive transport component is present.

An unstirred layer shifts the permeation curve due to a carrier-mediated transport system (non-passive component) to the right, so that a higher Km value is determined (apparent Michaelis constant biased by an unstirred layer). If a substance is transported simultaneously by a non-passive and a passive mechanism, and if the non-passive component can be inhibited, the permeation curve due to the non-passive component can be obtained by subtraction of the curve due to the passive component alone from the curve obtained with intact passive and non-passive component. But in the presence of an unstirred layer the difference curve lies always below the curve which would be obtained in the presence of the non-passive component alone. This error increases with increasing unstirred layer thickness and increasing magnitude of the passive transport component. By means of an appropriate equation the apparent Michaelis constant biased by an unstirred layer and determined from the difference curve can be corrected, if the unstirred layer thickness and area are known.

Biological Transport↗

Variations in presynaptic grid size in the granular and molecular layer of the cerebellar cortex of the cat. I. A quantitative ultrastructural study on semithin E-PTA sections.

The size distribution of synapses in the cerebellar cortex of the cat was defined on 0.5-micron semithin sections stained with ethanolic phosphotungstic acid (E-PTA). The surface area (SA) of synaptic grids was measured and the number of dense projections per grid (NDP) was counted. The results show large differences in mean values between molecular and granular layer. Within the molecular layer the differences in mean values at different levels below the pial surface were small; however, the frequency distributions differed significantly. In the granular layer a confined unimodal frequency distribution of SA and NDP was observed (mean NDP, 7.02 +/- 0.10), in the molecular layer a considerable variation in the size of the synaptic discs was observed (mean NDP, 20.40 +/- 0.43). Only a small percentage of the synaptic discs have less than 5 or more than 47 DPs. The sharply defined differences in synaptic size between the granular and molecular layer and the smaller differences within the granular and molecular layer are discussed in the context of the congruity hypothesis of Chan-Palay.

Animals↗

Projection of olfactory bulb efferents to layer I GABAergic neurons in the entorhinal area. Combination of anterograde degeneration and immunoelectron microscopy in rat.

Glutamic acid decarboxylase (GAD) immunoelectron microscopy in combination with anterograde degeneration was applied in rats to study the synaptic targets of olfactory bulb afferents to the lateral subdivision (LEA) of the entorhinal area (EA). Immunoreactive neurons and terminals are scattered throughout all layers of LEA. After olfactory bulb resection, terminal degeneration occurs in layer Ia of EA. Using the electron microscope we examined serial thin sections of 12 and 14 immunoreactive neurons sampled from layer Ia of the dorsal (DLEA) and ventral (VLEA) subdivisions of LEA, respectively. The morphology of all these neurons is similar: they are small (short axis 5-9 micron, long axis 7-12 micron) and possess eccentrically located, indented nuclei provided with filamentous nuclear rodlets. The immunoreactive neurons have thin, smooth dendrites which usually emerge abruptly from the somata. We observed a single cilium on 5 of the immunoreactive neurons. In layer Ia of both DLEA and VLEA, the somata of the immunoreactive neurons are contacted by degenerating, non-immunoreactive boutons showing asymmetric synaptic junctions. In addition to these boutons, 4 other categories of axo-somatic terminals can be distinguished: normal, non-immunoreactive boutons forming asymmetric synapses and containing spherical synaptic vesicles; normal, non-immunoreactive boutons with symmetric synapses and pleomorphic synaptic vesicles; normal, non-immunoreactive boutons with asymmetric synapses, containing dense-cored vesicles in addition to spherical synaptic vesicles; and normal, immunoreactive boutons with symmetric synapses and pleomorphic synaptic vesicles. It is suggested that the GAD-immunoreactive neurons which receive olfactory bulb input correspond to local circuit neurons with intralaminar axons which innervate each other as well as the distal segments of the apical dendrites of projection neurons with cell bodies in layers II and III. Thus, the olfactory input in EA seems to be wired not only for excitation of layers II and III pyramidal neurons but also for feed-forward inhibition using GABAergic intermediary neurons, strategically located in the area of termination of olfactory bulb fibers.

Animals↗

Serotonin (5-HT) induces IPSPs in pyramidal layer cells of rat piriform cortex: evidence for the involvement of a 5-HT2-activated interneuron.

In a slice preparation of rat piriform cortex, both intracellular and extracellular techniques were used to examine the pharmacological and electrophysiological actions of serotonin (5-HT). Bath application of 5-HT resulted in either depolarization (57%), hyperpolarization (34%) or no change (9%) in membrane potential of cells in the pyramidal cell layer (layer II) of piriform cortex. Additionally, when KCl-containing electrodes were used, 5-HT induced an increase in depolarizing synaptic potentials in 41% of these cells. It was concluded that these potentials were reverse inhibitory post-synaptic potentials (IPSPs) because they were blocked by bicuculline and tetrodotoxin. The induction of IPSPs by 5-HT was blocked by the 5-HT2-selective antagonist ritanserin. By recording extracellularly in the presence of 5-HT, a group of 5-HT-activated, putative interneurons was found at the border of layers II and III of piriform cortex, 5-HT but not norepinephrine activation was blocked by ritanserin. The actions of 5-HT were mimicked by the 5-HT2 agonist alpha-methyl-5-HT; the 5-HT2 partial agonist, 2,5-dimethoxy-4-methyl-amphetamine had a small agonist action of its own and blunted the effect of 5-HT. Activation of a larger group of putative interneurons by the more universal excitant N-methyl-D-aspartate showed that the 5-HT-activated interneurons represented 23% of the interneurons located on the border between layers II and III. We conclude that 5-HT induces IPSPs in layer II pyramidal cells by activating a subpopulation of interneurons at the border of layers II and III of piriform cortex.

Animals↗

The effects of selective glutamate receptor antagonists on synchronized firing bursts in layer III of rat visual cortex.

In the rat visual cortex in vitro, single-shock stimulations applied to the border between layer VI and the white matter evoke synchronized burst-firing by units in layer III. We have examined the effects of glutamate receptor antagonists on this activity, with antagonists applied via the bath to allow correlation of effects with concentrations. All synaptically driven components (recorded extracellularly as field potential 'S2' spikes, dipoles 'W1' and 'W2', and coinciding single-unit spikes) were inhibited by greater than 90% in 1.0 mM kynurenic acid and in 3 or 10 microM 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, which selectively blocks AMPA/kainate receptors). S2 spike amplitudes were reduced by half in 0.7 microM CNQX. 2-Amino-5-phosphonovalerate (APV), a specific blocker of NMDA receptors, did not prevent S2 spike burst or horizontal spread of bursting within layer III. However, APV reduced the duration of synchronized bursts and the slower potentials which followed. In Mg(2+)-free medium, new components appeared which were APV-sensitive: (1) low amplitude spikes, distributed spatially like S2 spike, but recurring more slowly, and (2) slow potentials, distributed spatially like W1 and W2 potentials, but lasting for hundreds of milliseconds. The amplitudes of these spikes were reduced by half in 3 microM D-APV. Our data imply that: (1) glutamate receptors play a major role in mediating local, excitatory neurotransmission in the supragranular layers of neocortex, with NMDA and AMPA/kainate subtypes each subserving somewhat different functions; (2) AMPA/kainate receptors mediate rapid excitatory transmission between layer III neurons, responsible for driving the first 15 ms of synchronized bursts; (3) currents gated by NMDA receptors determine the duration of coherent firing bursts, and drive asynchronous neuronal firing following bursts; and (4) under conditions which circumvent block by extracellular Mg2+, activation of NMDA receptors greatly enhances and prolongs the response to single-shock stimulations. In vivo, activation of layer III neurons is likely to depend significantly upon currents gated by NMDA receptors whenever repetitively firing excitatory inputs summed over several tens of milliseconds provide enough depolarization to lift block by extracellular Mg2+.

2-Amino-5-phosphonovalerate↗

Corticothalamic projections from layer V cells in rat are collaterals of long-range corticofugal axons.

The vast majority of corticothalamic (CT) axons projecting to sensory-specific thalamic nuclei arise from layer VI cells but intralaminar and associative thalamic nuclei also receive, to various degrees, a cortical input from layer V pyramidal cells. It is also well established that all long-range corticofugal projections reaching the brainstem and spinal cord arise exclusively from layer V neurons. These observations raise the possibility that the CT input from layer V cells may be collaterals of those long-range axons projecting below thalamic level. The thalamic projections of layer V cells were mapped at a single cell level following small microiontophoretic injections of biocytin performed in the motor, somatosensory and visual cortices in rats. Camera lucida reconstruction of these CT axons revealed that they are all collaterals of long-range corticofugal axons. These collaterals do not give off axonal branches within the thalamic reticular nucleus and they arborize exclusively within intralaminar and associative thalamic nuclei where they from small clusters of varicose endings. As layer V cells are involved in motor commands everywhere in the neocortex, these CT projections and their thalamic targets should be directly involved in the central organization of motor programs.

Animals↗

Acquisition of synchronous beating between embryonic heart cell aggregates and layers.

Synchronous beating between chick embryonic heart cell aggregates and heart cell layers was used to study the relationship between intercellular adhesion and ionic coupling. Adhesion was measured by counting the proportion of aggregates which were not to be removed from cell layers by gentle washing after a 30 min incubation. Synchrony between bound aggregates and contiguous layers was assessed by phase microscopy. The first evidence of synchrony was seen 1.5 h after addition of aggregates to layers, following which there was an increase in the percentage of aggregates beating synchronously, reaching over 50% at 7 h and slowly increasing to a maximum of 65% by 24 h. Scanning electron microscopy and autoradiography of thymidine-labeled cells suggest that synchrony does not depend on cell movement at the interface between aggregate and layer. Acquisition of synchrony can be prevented completely by inhibiting protein synthesis, although pulsation of aggregates and layers continues in proportions unchanged from controls. After reversal of protein synthesis inhibition, synchrony is acquired at a rate and to an extent closely resembling that of newly adherent controls. These data indicate that ionic coupling is neither an inevitable nor an immediate consequence of adhesion. Since ionic coupling has been shown to correlate with the presence of gap junctions, the findings suggest that gap junctions are not involved in the initial events responsible for intercellular adhesion in vitro and that their formation following adhesion in this system may depend upon protein synthesis.

Animals↗

Maternal ethanol consumption: lack of effect on synaptogenesis in layer I of the motor cortex in 19-day-old rat offspring.

Previous studies showed that in utero exposure to ethanol has an adverse effect on development of the central nervous system. Included among those abnormalities is the evidence that in utero exposure to ethanol alters the development of the cerebral cortex in terms of the arborization of pyramidal dendrites and the concentration of neurotransmitters and neurotransmitter receptors. However, limited information is available about the influence of in utero exposure to ethanol on synaptogenesis in the cortex. We examined the influence of chronic maternal ethanol consumption, prior to parturition, on synaptogenesis in layer I of the motor cortex of 19-day-old-rat offspring. Layer I (the molecular layer) was chosen because of the early timing of its development. The motor cortex was chosen because of the evidence of motor problems in children afflicted with the fetal alcohol syndrome. The results of these studies demonstrated that the 19-day-old offspring of rats that were pair-fed, using control or 6.6% (v/v) ethanol-containing liquid diets on a chronic basis prior to parturition, had a comparable density of synapses and distribution of paramembranous density lengths in layer I of the motor cortex as well as a comparable thickness of cortical layer I. Thus, evidence by this and other laboratories, of cortical neurotransmitter and dendritic abnormalities are not reflected in synaptic changes in layer I of the motor cortex at 19 days. It is possible that synaptogenesis is affected at another age or in other regions of the cerebral cortex.

Animals↗

Effects of specimen load-bearing and free surface layers on the compressive mechanical properties of cellular materials.

The influence of load-bearing surface layers on Young's modulus was determined for cancellous bone and polyurethane foam specimens of three different heights cut from each material: 16, 9, and 5 mm for bone specimens (cross-sectional area A = 81 mm2) ranging in density from 0.04 to 0.32 g cm-3; 20, 10, and 5 mm for foam specimens (A = 100 mm2) ranging in density from 0.064 to 0.64 g cm-3. The compressive elastic modulus of the 5 mm bone specimens was significantly smaller (42%) than that of the 16 mm bone specimens. A similar change in elastic modulus was also observed for the foam specimens, but the height effect diminished in a relatively linear manner as the foam density increased. For a height change from 20 to 5 mm, the foam modulus difference ranged from a 41% decrease for the lowest density specimens (p = 0.064 g cm-3) to an insignificant change (< 1.8%) for the highest foam density specimens (p = 0.64 g cm-3). The specimen height effect on elastic modulus was hypothesized to result from a higher deformation (compliance) of the cellular materials in the load-bearing or contacting surface layer than in the bulk. A mathematical formula was derived to predict the variation in measured elastic modulus (E) caused by the contacting surface layer modulus (Ecs) to bulk modulus (Eb) ratio (Y = Ecs/Eb) and contacting surface layer height (hcs) to sample height (h) ratio (t = hcs/h): E/Eb = Y/[Y(1-t)+t]. Predicted differences in the measured modulus associated with graduated specimen heights were verified experimentally by regional strain measurements of the foam and bone samples using an optical microscope. The influence of free-surface layers was also determined for the foam specimens with cross-sectional areas 1.21 and 10 times the load-bearing area of a load platen, but the measured differences were small (< 10%) compared to that of the load-bearing surface layer influence. In future compressive mechanical testing of cellular materials, specimens < 10 mm in height should be avoided, particularly specimens with low bulk density or high porosity.

Adult↗

Rigor crossbridge structure in tilted single filament layers and flared-X formations from insect flight muscle.

The averaged structure of rigor crossbridges in insect flight muscle has been studied in filtered images. Their three-dimensional structure has been deduced by relating tilt views of single filament layers in 25 nm longitudinal sections (myac layers and actin layers) to the flared-X appearance in 15 nm cross-sections showing single crossbridge levels. Tilting myac or actin layers around the filament axis makes crossbridges show one of two patterns. Beadlike densities appear either singly over thin filaments ("center-beading") or doubled and flanking thin filaments ("straddle-beading"). These express two different projections from the crossbridge-actin complexes as seen end-on in flared-X formations. Tannic acid/glutaraldehyde fixation gave improved actin preservation, showing, in 15 nm cross-sections, the long-pitch helical strands as "two-dot" profiles of consistent azimuth in the gaps between double chevrons. The azimuth in the flared-X arms was then inferred from lattice relationships, since it was not seen directly. The tangential attachment of comma-shaped crossbridges to the inferred actin dyad fits the binding geometry in recent actin-subfragment 1 complex reconstructions. However, averaged crossbridge structure differs between lead and rear members of double chevrons, unlike the uniform heads on decorated actin. In filtered images of myac layers, the lead bridges are dense and steeply angled; the rear chevron is seen as a dense bead over the thin filament with faint, less angled bars extending laterally. Actin layer images also suggest that rear and lead bridges differ in angle. Left and right flared-X arms are end-on views of lead and rear chevron bridges, respectively, and differ in shape. Improved fixation with tannic acid/glutaraldehyde allows us to distinguish three crossbridge domains in flared-X arms: (1) a dense bulb-like head merged into the thin filament; (2) a dense but thinner neck tangential to actin; and (3) a faint thin stem joining the necks to myosin filaments. Shape differences in lead and rear members between the head-neck-actin complexes are indicated by the names "L sigmoid" and "R dogleg". Within crossbridges, internal angles between the head-neck axis and the head-actin-head axis differ between sigmoid and dogleg by about 30 degrees, implying a flexible junction between bridge-head and bridge-neck. Lead and rear bridges are axially at least 13 nm apart on actin; the expected 60 degrees difference in azimuth is expressed by head-neck portions, but the head-actin-head axis rotates by only 30 degrees.(ABSTRACT TRUNCATED AT 400 WORDS)

Actins↗

Correlation between extrinsic nerve fibers and synapses in the muscle layers of bowels affected by Hirschsprung's disease.

The aim of this study is to clarify any correlation between nerve terminals (synapses) and proliferating extrinsic nerve fibers in the muscle layers of bowels affected by Hirschsprung's disease (HD). Synapses and extrinsic nerve fibers in the muscle layers of bowels of 10 patients with HD and 8 comparable controls were labeled with monoclonal antibody (MAb) 171B5 and acetylcholinesterase (AChE), respectively. In the control a rich and even distribution of synapses, representing neuromuscular junctions, was seen in the muscle layers, together with dense clusters of synapses in the adjacent myenteric plexuses; proliferation of extrinsic nerve fibers was not seen. In the transitional oligoganglionic segment of HD, many synapses were present in the myenteric plexus, but a few synapses in the muscle layers; there was a gradual increase of extrinsic nerve fibers from proximal to distal. In the narrow aganglionic segment very few synapses were seen in the muscle layers; proliferating nerve fibers and bundles were prominent. We conclude that the muscle layers of bowels affected by HD were almost denervated despite presence of intrinsic nervous elements in the oligoganglionic segment and proliferating extrinsic nerve fibers in the aganglionic segment.

Hirschsprung Disease↗

Development of peritoneal fibrosis occurs under the mesothelial cell layer.

This study was carried out in order to find out which part of the peritoneal wall reacts toward silica and produces peritoneal fibrosis. Colloidal silica was injected into the peritoneal cavity of rats to induce chemical peritonitis and frozen sections of the peritoneal wall were stained with specific antibodies toward type I and III collagens and fibronectin. A massive proliferation of granulation tissue was observed between the submesothelial and muscular layers within 48 hr visualized by prominent fibronectin staining. Type III collagen formed lamellar-like structures in the newly formed granulation tissue. The connective tissue reaction was extended into the underlying muscular tissue. Three weeks after silica injection the reactive granulation tissue exceeded the original peritoneum three- to fourfold in thickness. At this stage it contained extended fibrillar structures oriented perpendicular to the surface or muscular layers of the peritoneum. Type I collagen antibody was bound to the superficial cell layer in the control samples and in the early peritonitis whereas the entire granulation tissue was evenly stained at 3 weeks. Type III collagen antibody was bound to the surface layer of the peritoneum, granulation tissue, and perimysial connective tissue throughout the healing period. The results indicate that the peritoneal fibrotic process occurs under the thin peritoneal lining cell layer and on the surface of the muscle layer.

Animals↗

A freeze-fracture study of the papillary layer of the rat incisor enamel organ.

After tooth enamel has been secreted it undergoes maturation or hardening. This process is mediated by ruffled and smooth-ended ameloblasts and associated papillary layer cells. The cells of the papillary layer are characterized by large numbers of mitochondria, coated vesicles, microvilli, and gap junctions. These features have led numerous investigators to speculate that the papillary layer is an ion-transporting epithelium. We have conducted freeze-fracture studies of the rat papillary layer in order to better characterize the surface features of these cells. The cell membranes of the papillary cells contained large numbers of intramembrane particles of various sizes ranging from 4 to 9 nm in diameter. Gap junctions were present at the cell surface and in the cytoplasm in the form of annular gap junctions. The intramembrane particles or connexons of both types of gap junctions were about 8-9 nm wide and were either packed randomly or present in the so-called 'crystallized' state. At the interface between smooth-ended ameloblasts and papillary layer cells, a well-developed zonula occludens was present along the basal surfaces of the ameloblasts and several large gap junctions were formed between the two cell types. The capillary network associated with the papillary layer was characterized by a thin endothelium containing large numbers of fenestrations.

Animals↗