Ultrastructural Characteristics of Capillaries Entering and Leaving the Stria Vascularis

1986 ◽  
Vol 95 (3) ◽  
pp. 309-312 ◽  
Author(s):  
Kensuke Watanabe
Keyword(s):  
Horseradish Peroxidase ◽  
Basal Cell ◽  
Stria Vascularis ◽  
The Other ◽  
Spiral Ligament ◽  
Perivascular Spaces ◽  
Basal Cells ◽  
Vascular Flow ◽  
Cell Layers ◽  
Ultrastructural Characteristics

Capillaries entering and leaving the stria vascularis were surrounded by layers of basal cells and fibrocytes. The entering capillaries were surrounded by one or two thin basal cells, while the leaving capillaries were surrounded by four or five thicker and interdigitated basal cell layers. Moreover, the layers surrounding the leaving capillaries persisted further into the spiral ligament. Two kinds of filaments were observed in the basal cells, one thin and the other thick. Capillaries were observed to leak horseradish peroxidase before they entered and after they left the stria vascularis. Although the reaction product of horseradish peroxidase was observed in all perivascular spaces of leaving capillaries, very little or no reaction product was observed around some entering capillaries. It is speculated that the layers of basal cells and fibrocytes around entering and leaving capillaries control the vascular flow out of the stria vascularis, although the layers around leaving capillaries may be more contractile than those around entering capillaries.

Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear

Development ◽  
1989 ◽  
Vol 107 (3) ◽  
pp. 453-463 ◽  
Author(s):  
K.P. Steel ◽  
C. Barkway
Keyword(s):  
Neural Crest ◽  
Basal Cell ◽  
Stria Vascularis ◽  
Normal Adult ◽  
Basal Cells ◽  
Cochlear Duct ◽  
Cell Layers ◽  
Marginal Cells ◽  
Intermediate Cells ◽  
And Function

The stria vascularis of the mammalian cochlea is composed primarily of three types of cells. Marginal cells line the lumen of the cochlear duct and are of epithelial origin. Basal cells also form a continuous layer and they may be mesodermal or derived from the neural crest. Intermediate cells are melanocyte-like cells, presumably derived from the neural crest, and are scattered between the marginal and basal cell layers. The marginal cells form extensive interdigitations with the basal and intermediate cells in the normal adult stria. The stria also contains a rich supply of blood vessels. We investigated the role of melanocytes in the stria vascularis by studying its development in a mouse mutant, viable dominant spotting, which is known to have a primary neural crest defect leading to an absence of recognisable melanocytes in the skin. Melanocytes were not found in the stria of most of the mutants examined, and from about 6 days of age onwards a reduced amount of interdigitation amongst the cells of the stria was observed. These ultrastructural anomalies were associated with strial dysfunction. In the normal adult mammal, the stria produces an endocochlear potential (EP), a resting dc potential in the endolymph in the cochlear duct, which in mice is normally about +100 mV. In our control mice, EP rose to adult levels between 6 and 16 days after birth. In most of the mutants we studied, EP was close to zero at all ages from 6 to 20 days. Melanocyte-like cells appear to be vital for normal stria vascularis development and function. They may be necessary to facilitate the normal process of interdigitation between marginal and basal cell processes at a particular stage during development, and the lack of adequate interdigitation in the mutants may be the cause of their strial dysfunction. Alternatively, melanocytes may have some direct, essential role in the production of an EP by the stria. Melanocytes may be important both for normal strial development and for the production of the EP. We believe this is the clearest demonstration yet of a role for migratory melanocytes other than their role in pigmentation.

Change in the Capillary Permeability of the Stria Vascularis by Different Methods of Death and Fixation

1986 ◽  
Vol 95 (4) ◽  
pp. 427-431 ◽  
Author(s):  
Kensuke Watanabe
Keyword(s):  
Horseradish Peroxidase ◽  
Capillary Permeability ◽  
Stria Vascularis ◽  
Perivascular Spaces ◽  
Group 4 ◽  
Acute Anoxia ◽  
Group 3 ◽  
Group 2 ◽  
Almost All ◽  
Group 1

The permeability of the stria vascularis to horseradish peroxidase (HRP) was examined. Ten minutes after an intravenous injection of HRP, 15 guinea pigs were killed and fixed by four different methods: 1) cochleas fixed 3 minutes after decapitation, 2) administration of an overdose of pentobarbital, 3) cochleas fixed for 5 minutes before decapitation, and 4) cochleas fixed immediately after decapitation. In the animals in group 1, HRP leakage was observed in almost all strial vessels (86%), and blood sludging and amorphous HRP reaction product in 98% of strial capillaries. In the animals in group 2, strial capillaries were observed both with noticeable HRP leakage and with no evidence of leakage. Blood sludging was associated with amorphous HRP reaction product, while no blood sludging was associated with granular HRP reaction product. In group 3 animals, only faint or no HRP reaction product was observed in the perivascular spaces. Only 3% of the capillaries had blood sludging. In the animals in group 4, blood sludging but no HRP leakage was observed in almost all capillaries (82%). It is speculated that HRP does not normally leak from the strial capillaries, although many researchers have reported to the contrary. It appears that HRP leaks from the strial capillaries only when acute anoxia or hypotension continues for a few minutes. These conditions induce blood sludging and are followed by the appearance of many marginal folds in these capillaries.

Intercellular Fluid Pathways in the Organ of Corti of Cat and Man

1979 ◽  
Vol 88 (1) ◽  
pp. 2-11 ◽  
Author(s):  
Joseph B. Nadol
Keyword(s):  
Stria Vascularis ◽  
Organ Of Corti ◽  
Intercellular Junctions ◽  
Morphological Evidence ◽  
Spiral Ligament ◽  
Basal Cells ◽  
Scala Tympani ◽  
Supporting Cells ◽  
Cochlear Duct ◽  
Scala Vestibuli

The intercellular junctions in the organ of Corti of cat and man were examined with the electron microscope. In contrast to the zone of tight junctions, or zonulae occludentes, which were present at the surface of cells lining the scala media, there was no tight junctional specialization among the cells of the tympanic lamina, perilymphatic lining cells of the scala vestibuli, basal processes of the supporting cells of the organ of Corti or cells of the spiral limbus and spiral ligament. These findings suggest the possibility of fluid continuity between the scala vestibuli and scala tympani all along the cochlear duct. Morphological evidence for an intercellular diffusion barrier was present only at the endolymphatic surfaces of the cochlear duct and between the processes of the basal cells of the stria vascularis in cat and man.

scholarly journals Tissue-Specific Transcriptomes Reveal Gene Expression Trajectories in Two Maturing Skin Epithelial Layers in Zebrafish Embryos

2019 ◽  
Vol 9 (10) ◽  
pp. 3439-3452 ◽  
Author(s):  
Shawn J. Cokus ◽  
Maricruz De La Torre ◽  
Eric F. Medina ◽  
Jeffrey P. Rasmussen ◽  
Joselyn Ramirez-Gutierrez ◽  
...  
Keyword(s):  
Gene Expression ◽  
Epithelial Cells ◽  
Basal Cell ◽  
Building Blocks ◽  
Cell Types ◽  
Basal Cells ◽  
Skin Cells ◽  
Genes Encoding ◽  
Cell Layers ◽  
Epithelial Layers

Epithelial cells are the building blocks of many organs, including skin. The vertebrate skin initially consists of two epithelial layers, the outer periderm and inner basal cell layers, which have distinct properties, functions, and fates. The embryonic periderm ultimately disappears during development, whereas basal cells proliferate to form the mature, stratified epidermis. Although much is known about mechanisms of homeostasis in mature skin, relatively little is known about the two cell types in pre-stratification skin. To define the similarities and distinctions between periderm and basal skin epithelial cells, we purified them from zebrafish at early development stages and deeply profiled their gene expression. These analyses identified groups of genes whose tissue enrichment changed at each stage, defining gene flow dynamics of maturing vertebrate epithelia. At each of 52 and 72 hr post-fertilization (hpf), more than 60% of genes enriched in skin cells were similarly expressed in both layers, indicating that they were common epithelial genes, but many others were enriched in one layer or the other. Both expected and novel genes were enriched in periderm and basal cell layers. Genes encoding extracellular matrix, junctional, cytoskeletal, and signaling proteins were prominent among those distinguishing the two epithelial cell types. In situ hybridization and BAC transgenes confirmed our expression data and provided new tools to study zebrafish skin. Collectively, these data provide a resource for studying common and distinguishing features of maturing epithelia.

Stria Ultrastructure and Vessel Transport in Acoustic Trauma

1974 ◽  
Vol 83 (4) ◽  
pp. 498-514 ◽  
Author(s):  
Arndt J. Duvall ◽  
W. Dixon Ward ◽  
Kathryn E. Lauhala
Keyword(s):  
Horseradish Peroxidase ◽  
Stria Vascularis ◽  
Membrane System ◽  
Acoustic Trauma ◽  
Consistent Pattern ◽  
The Other ◽  
Intravenous Injections ◽  
Significant Damage ◽  
Intermediate Cells ◽  
Ultrastructural Abnormality

One hundred and ten chinchillas were exposed to a 700–2800 Hz noise at 123 dB for 15 minutes. A consistent pattern of ultrastructural pathology within the lateral cochlear wall was found. Significant damage to the stria vascularis was first observed one hour postexposure, reached a peak at 24 hours, and had recovered almost completely by 28 days. Spiral prominence damage was permanent. The pathology included stria widening, temporary disappearance of intermediate cells, alterations of the internal membrane system and abnormal vessel transport. Horseradish peroxidase (HRP) was employed as an indicator of transport from vessels. Transport from the stria vessels was absent when stria ultrastructural abnormality was at a maximum; at other postexposure times, however, abnormally rapid exodus of HRP from the vessels of the stria was observed in animals who had received intravenous injections of HRP 30 seconds prior to sacrifice. On the other hand, no leakage was observed in the animals injected one minute before sacrifice. Theories to explain this transport dichotomy are proposed.

Comparative Measurements of Cochlear Apparatus

1968 ◽  
Vol 11 (2) ◽  
pp. 229-235 ◽  
Author(s):  
Makoto Igarashi ◽  
Robert G. Mahon ◽  
Shizuo Konishi
Keyword(s):  
Cross Section ◽  
Basilar Membrane ◽  
Stria Vascularis ◽  
The Other ◽  
Tectorial Membrane ◽  
Spiral Ligament ◽  
Scala Tympani ◽  
Basal Turn ◽  
Temporal Bones ◽  
Scala Vestibuli

Micromeasurements of horizontal midmodiolar sections of temporal bones were performed to obtain the dimensions of the different cochlear partitions in the squirrel monkey, the cat, and the rat. The width of the basilar membrane and the tectorial membrane were larger in the apical turn than in the basal turn in all three species. The thickness of the spiral ligament, the width of Reissner’s membrane, and the width of the stria vascularis were larger in the basal turn than in the apical turn. The cross-section areas of scala vestibuli and scala tympani in the three species were larger in the basal turn than in the other turns.

Distribution and significance of endothelin 1 in guinea pig cochlear lateral wall

2007 ◽  
Vol 121 (8) ◽  
pp. 721-724 ◽  
Author(s):  
D-Y Xu ◽  
Y-D Tang ◽  
S-X Liu ◽  
J Liu
Keyword(s):  
Guinea Pig ◽  
Stria Vascularis ◽  
Lateral Wall ◽  
Complex Method ◽  
Spiral Ligament ◽  
Basal Cells ◽  
Endothelin 1 ◽  
Marginal Cells ◽  
Spiral Ligament Fibrocytes ◽  
Avidin Biotin Complex

AbstractEndothelin 1 is a vasoconstrictive peptide with many biological functions. To investigate the distribution of endothelin 1 in guinea pig cochlear lateral wall and the significance of endothelin 1 in maintaining cochlear homeostasis, the immunohistochemistry avidin biotin complex method was applied by using rabbit anti-endothelin 1 polyclonal antibody as primary antibody. Endothelin-1-like activities were detected in the marginal cells, spiral prominence epithelial cells, outer sulcus cells, stria vascularis capillaries, basal cells and spiral ligament fibrocytes.These results suggest that endothelin 1 may play an important role in maintaining cochlear homeostasis.

Comparative strengths and weaknesses of peroxidase and colloidal gold in pre- and post-embedding immunolabeling techniques

1987 ◽  
Vol 45 ◽  
pp. 1002-1005
Author(s):  
D. R. Abrahamson ◽  
P. L. St.John ◽  
E. W. Perry
Keyword(s):  
Electron Microscopy ◽  
Horseradish Peroxidase ◽  
Light Microscopy ◽  
Colloidal Gold ◽  
Light Microscope ◽  
Ultrastructural Localization ◽  
The Other ◽  
Quantitative Studies ◽  
Dense Suspension ◽  
Antigen Localization

Antibodies coupled to tracers for electron microscopy have been instrumental in the ultrastructural localization of antigens within cells and tissues. Among the most popular tracers are horseradish peroxidase (HRP), an enzyme that yields an osmiophilic reaction product, and colloidal gold, an electron dense suspension of particles. Some advantages of IgG-HRP conjugates are that they are readily synthesized, relatively small, and the immunolabeling obtained in a given experiment can be evaluated in the light microscope. In contrast, colloidal gold conjugates are available in different size ranges and multiple labeling as well as quantitative studies can therefore be undertaken through particle counting. On the other hand, gold conjugates are generally larger than those of HRP but usually can not be visualized with light microscopy. Concern has been raised, however, that HRP reaction product, which is exquisitely sensitive when generated properly, may in some cases distribute to sites distant from the original binding of the conjugate and therefore result in spurious antigen localization.

scholarly journals Extracellular vesicles from human airway basal cells respond to cigarette smoke extract and affect vascular endothelial cells

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ashish Saxena ◽  
Matthew S. Walters ◽  
Jae-Hung Shieh ◽  
Ling-Bo Shen ◽  
Kazunori Gomi ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Cigarette Smoke ◽  
Extracellular Vesicles ◽  
Basal Cell ◽  
Mapk Signaling ◽  
Cigarette Smoke Extract ◽  
Vegf Receptor ◽  
Vascular Endothelial ◽  
Basal Cells ◽  
Human Airway

AbstractThe human airway epithelium lining the bronchial tree contains basal cells that proliferate, differentiate, and communicate with other components of their microenvironment. One method that cells use for intercellular communication involves the secretion of exosomes and other extracellular vesicles (EVs). We isolated exosome-enriched EVs that were produced from an immortalized human airway basal cell line (BCi-NS1.1) and found that their secretion is increased by exposure to cigarette smoke extract, suggesting that this stress stimulates release of EVs which could affect signaling to other cells. We have previously shown that primary human airway basal cells secrete vascular endothelial growth factor A (VEGFA) which can activate MAPK signaling cascades in endothelial cells via VEGF receptor–2 (VEGFR2). Here, we show that exposure of endothelial cells to exosome-enriched airway basal cell EVs promotes the survival of these cells and that this effect also involves VEGFR2 activation and is, at least in part, mediated by VEGFA present in the EVs. These observations demonstrate that EVs are involved in the intercellular signaling between airway basal cells and the endothelium which we previously reported. The downstream signaling pathways involved may be distinct and specific to the EVs, however, as increased phosphorylation of Akt, STAT3, p44/42 MAPK, and p38 MAPK was not seen following exposure of endothelial cells to airway basal cell EVs.

scholarly journals Progenitor identification and SARS-CoV-2 infection in long-term human distal lung organoid cultures

2020 ◽  
Author(s):  
Ameen A. Salahudeen ◽  
Shannon S. Choi ◽  
Arjun Rustagi ◽  
Junjie Zhu ◽  
Sean M. de la O ◽  
...  
Keyword(s):  
Lung Disease ◽  
Single Cell ◽  
Basal Cell ◽  
Human Lung ◽  
Basal Cells ◽  
Ciliated Cells ◽  
Club Cells ◽  
Distal Lung

ABSTRACTThe distal lung contains terminal bronchioles and alveoli that facilitate gas exchange and is affected by disorders including interstitial lung disease, cancer, and SARS-CoV-2-associated COVID-19 pneumonia. Investigations of these localized pathologies have been hindered by a lack of 3D in vitro human distal lung culture systems. Further, human distal lung stem cell identification has been impaired by quiescence, anatomic divergence from mouse and lack of lineage tracing and clonogenic culture. Here, we developed robust feeder-free, chemically-defined culture of distal human lung progenitors as organoids derived clonally from single adult human alveolar epithelial type II (AT2) or KRT5+ basal cells. AT2 organoids exhibited AT1 transdifferentiation potential, while basal cell organoids progressively developed lumens lined by differentiated club and ciliated cells. Organoids consisting solely of club cells were not observed. Upon single cell RNA-sequencing (scRNA-seq), alveolar organoids were composed of proliferative AT2 cells; however, basal organoid KRT5+ cells contained a distinct ITGA6+ITGB4+ mitotic population whose proliferation segregated to a TNFRSF12Ahi subfraction. Clonogenic organoid growth was markedly enriched within the TNFRSF12Ahi subset of FACS-purified ITGA6+ITGB4+ basal cells from human lung or derivative organoids. In vivo, TNFRSF12A+ cells comprised ~10% of KRT5+ basal cells and resided in clusters within terminal bronchioles. To model COVID-19 distal lung disease, we everted the polarity of basal and alveolar organoids to rapidly relocate differentiated club and ciliated cells from the organoid lumen to the exterior surface, thus displaying the SARS-CoV-2 receptor ACE2 on the outwardly-facing apical aspect. Accordingly, basal and AT2 “apical-out” organoids were infected by SARS-CoV-2, identifying club cells as a novel target population. This long-term, feeder-free organoid culture of human distal lung alveolar and basal stem cells, coupled with single cell analysis, identifies unsuspected basal cell functional heterogeneity and exemplifies progenitor identification within a slowly proliferating human tissue. Further, our studies establish a facile in vitro organoid model for human distal lung infectious diseases including COVID-19-associated pneumonia.

Sign in / Sign up

Export Citation Format

Share Document