2.The effects on inhibition of corneal neovascularization after human amniotic membrane transplantation in severely damaged rabbit corneas.
Jae Chan KIM ; Scheffer C G TSENG
Korean Journal of Ophthalmology 1995;9(1):32-46
Human amniotic membrane isolated from the placenta contained basement membrane components such as type IV collagen, laminin, and 6 and 4 integrins, all of which remained detectable while preserved in glycerin for one week. One month after the n-heptanol removal of the total corneal epithelium and the limbal lamellar keratectomy, all rabbit eyes carried features of limbal deficiency, including conjunctival epithelial ingrowth, vascularization and chronic inflammation. Ten control eyes then received a total keratectomy, and 13 experimental eyes received an additional amniotic membrane transplantation. Three-month follow-ups revealed that all control corneas were revascularized to the center with granuloma and retained a conjunctival phenotype. In contrast, in the experimental groups, 5 corneas became clear with either minimal or no vascularization; the rest had either mild peripheral (5) or total (3) vascularization and more cloudy stroma. Using monoclonal antibodies for epithelial markers and matrix components, we concluded that the success correlated with the return of a cornea-like epithelial phenotype and the preservation of the amniotic membrane, whereas the failure maintained a conjunctival epithelial phenotype and the amniotic membrane was either partially degraded or covered by host fibrovascular stroma. Measures taken to facilitate the former might prove this procedure clinically useful for ocular surface reconstruction.
Amnion/chemistry/*transplantation
;
Animals
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Antibodies, Monoclonal
;
Basement Membrane/chemistry/pathology
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Cornea/pathology/*surgery
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Corneal Neovascularization/pathology/*prevention & control/surgery
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Epithelium/pathology/surgery
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Extracellular Matrix Proteins/analysis
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Female
;
Fluorescent Antibody Technique
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Humans
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Immunophenotyping
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Male
;
Rabbits
3.Nature and histogenesis of pulmonary sclerosing hemangioma.
Chinese Journal of Pathology 2004;33(2):168-170
Apoproteins
;
analysis
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Epithelium
;
chemistry
;
ultrastructure
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Humans
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Lung
;
chemistry
;
pathology
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Nuclear Proteins
;
analysis
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Pulmonary Sclerosing Hemangioma
;
chemistry
;
pathology
;
Pulmonary Surfactant-Associated Proteins
;
analysis
;
Secretory Component
;
analysis
;
Thyroid Nuclear Factor 1
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Transcription Factors
;
analysis
4.Expression of HLA-DR antigen in large bowel carcinoma.
Eun Sook CHANG ; Soo Sang SOHN
Journal of Korean Medical Science 1995;10(5):334-341
One hundred large bowel carcinomas were studied immunohistochemically with regard to expression of HLA-DR antigen (DR). One or two sections from each tumor including surrounding normal mucosa were examined by a semiquantitative counting system for tumor cells and mucosal and stromal infiltrates of lymphocytes and mononuclear cells (MNCs) with DR expression and the results were applied Chi-square test. The rate of presence of DR positive (DR+) lymphocytes in lymphoid nodules and DR+ lymphocytes/ MNC in the adjacent mucosa and stroma in DR+ carcinoma (50%) was higher (P < 0.01) than in DR- carcinoma (21.9%). Thirty-six carcinomas (36%) were DR+. Three (75%) out of 4 DR+ poorly differentiated carcinomas and six (20%) out of 30 DR+ moderately differentiated carcinomas showed homogeneously strong DR+ expression. There was tendency for poorly differentiated carcinoma to be more homogeneous DR+ expression. According to Dukes' stage, four (80%) out of 5 carcinomas in Dukes' stage D were DR-. An increased infiltration of lymphocytes/MNCs into adjacent mucosa and stroma in large bowel carcinomas is possibly related with DR expression by carcinoma. From the results of this study, we postulated as follows: 1) DR+ tumor cells may act as antigen-presenting cells, 2) They may have an inhibitory effect for distant metastasis, 3) Poorly differentiated carcinoma expressed more DR+ homogeneously.
Adult
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Aged
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Antibodies
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Colorectal Neoplasms/blood/*chemistry/pathology
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Epithelium/chemistry
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Female
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HLA-DR Antigens/*analysis
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Human
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Immunohistochemistry
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Leukocytes, Mononuclear/chemistry
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Lymphocytes/chemistry
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Male
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Middle Age
;
Neoplasm Staging
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Support, Non-U.S. Gov't
5.Hypoxia Increases Epithelial Permeability in Human Nasal Epithelia.
Hyun Jin MIN ; Tae Hoon KIM ; Joo Heon YOON ; Chang Hoon KIM
Yonsei Medical Journal 2015;56(3):825-831
PURPOSE: The nasal mucosa is the first site to encounter pathogens, and it forms continuous barriers to various stimuli. This barrier function is very important in the innate defense mechanism. Additionally, inflammation of the nasal sinus is known to be a hypoxic condition. Here, we studied the effect of hypoxia on barrier function in normal human nasal epithelial (NHNE) cells. MATERIALS AND METHODS: The expression levels of various junction complex proteins were assessed in hypoxia-stimulated NHNE cells and human nasal mucosal tissues. We performed real-time polymerase chain reaction analysis, western blotting, and immunofluorescence assays to examine differences in the mRNA and protein expression of ZO-1, a tight junction protein, and E-cadherin in NHNE cells. Moreover, we evaluated the trans-epithelial resistance (TER) of NHNE cells under hypoxic conditions to check for changes in permeability. The expression of ZO-1 and E-cadherin was measured in human nasal mucosa samples by western blotting. RESULTS: Hypoxia time-dependently decreased the expression of ZO-1 and E-cadherin at the gene and protein levels. In addition, hypoxia decreased the TER of NHNE cells, which indicates increased permeability. Human nasal mucosa samples, which are supposed to be hypoxic, showed significantly decreased levels of ZO-1 and E-cadherin expression compared with control. CONCLUSION: Our results demonstrate that hypoxia altered the expression of junction complex molecules and increased epithelial permeability in human nasal epithelia. This suggests that hypoxia causes barrier dysfunction. Furthermore, it may be associated with innate immune dysfunction after encountering pathogens.
Anoxia/etiology/*metabolism
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Blotting, Western
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Cadherins/*analysis/genetics
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Epithelium/chemistry/pathology
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Humans
;
Membrane Proteins/*analysis
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Nasal Mucosa/*chemistry/pathology/*secretion
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Permeability/*radiation effects
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RNA, Messenger/genetics/metabolism
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Real-Time Polymerase Chain Reaction
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Tight Junctions/*metabolism
;
Zonula Occludens-1 Protein
6.Histopathological study on allergic rhinitis treated with Centipeda minima.
Zhi-gang LIU ; Hong-mong YU ; Shan-li WEN ; Yu-ling LIU
China Journal of Chinese Materia Medica 2005;30(4):292-294
OBJECTIVEThe aim of this study was to investigate the mechanisms of C. minima in the treatment of allergic rhinitis.
METHODAn allergic rhinitis animal model induced by ragweed pollen was established. After treatment with an active extract of C. minima, histopathological changes in the nasal mucosa of guinea pig were observed by transmission electron microscope.
RESULTIn the allergeic rhinitis model group, there appear a large number of lysosomes in the nasal epithelium with organelles vacuolated and nucleus deformed. Cells in the proper lamina of connective tissue were disarranged with organelles damaged, and there was also infiltration of eosinophils and mast cells in the connective tissue. However, in the treatment group receiving C. minima extract, the pathological changes mentioned above were significantly decreased.
CONCLUSIONC. minima is effective in treating allergic rhinitis.
Animals ; Asteraceae ; chemistry ; Epithelium ; ultrastructure ; Female ; Guinea Pigs ; Lysosomes ; drug effects ; Male ; Mitochondrial Swelling ; drug effects ; Nasal Mucosa ; pathology ; ultrastructure ; Oils, Volatile ; isolation & purification ; pharmacology ; Phytotherapy ; Plants, Medicinal ; chemistry ; Rhinitis, Allergic, Seasonal ; drug therapy ; pathology
7.Expression of extracellular matrix proteins and vimentin in testes of azoospermic man: an immunohistochemical and morphometric study.
Kemal Hakan GÜLKESEN ; Tibet ERDOĞRU ; Canan Figen SARGIN ; Gülten KARPUZOĞLU
Asian Journal of Andrology 2002;4(1):55-60
AIMTo investigate the changes in the extracellular matrix protein expression and the morphology of seminiferous tubules in the testis of 88 azoospermic men.
METHODSThe patients were of the following categories: (1) 22 cases of Sertoli-cell-only syndrome, (2) 20 cases of spermatogenic arrest, and (3) 46 cases with hypospermatogenesis. Testicular sections were immunohistochemically stained for fibronectin, vimentin, laminin and collagen type IV. The seminiferous tubular diameter and the connective matrix zone (CMZ, the acellular zone between the basement membrane [BM] and the peritubular cells) thickness were measured. Seminiferous tubules were typed according to the thickness of the connective matrix in the lamina propria. The predominant tubule type and the Johnsen and Silber scores were determined.
RESULTSThe mean tubular diameter were 119 +/- 27, 117 +/- 20, and 140 +/- 38 microm for Groups 1, 2, and 3, respectively. Both the laminin and the type IV collagen were localized to the epithelial BM and peritubular cells. In most of the tubules, BM and peritubular cells were separated by a homogenous acellular layer, the CMZ, in which laminin, type IV collagen, fibronectin and vimentin were not present. It is perceived that the worse the testicular histology, the higher the thickness of the CMZ.
CONCLUSIONIn testis with no or low sperm production, the diameter of the seminiferous tubules is decreased, the thickness of the seminiferous tubular wall is increased and a CMZ is formed between the peritubular cells and the BM. The thickness of CMZ is increasing with the advancement of testiclar deterioration. The most important morphologic predictive factor for spermiogenesis is the predominant
Adult ; Collagen Type IV ; analysis ; biosynthesis ; Extracellular Matrix Proteins ; analysis ; biosynthesis ; Fibronectins ; analysis ; biosynthesis ; Humans ; Immunohistochemistry ; Laminin ; analysis ; biosynthesis ; Logistic Models ; Male ; Middle Aged ; Oligospermia ; metabolism ; pathology ; Seminiferous Epithelium ; metabolism ; pathology ; Spermatogenesis ; Testis ; chemistry ; metabolism ; pathology ; Vimentin ; analysis ; biosynthesis