No abstract available.
Dermoid Cyst*

No abstract available.
Angiomyoma*

PURPOSE: The growth hormone receptor(GHR) is essential for the actions of growth hormone on postnatal growth and metabolism. GHR transcripts are characterized by the presence of disparate 5'untranslated exons. In contrast to L1 transcript, factors regulating the expression of the GC rich L2 transcript have remained unidentified. The purpose of this study is in order to characterize the mechanisms regulating expression of the L2 transcript in the murine GHR gene METHODS: Transient transfection experiments including deletional analysis and co-transfection assay were performed to find a region containing promoter activity in the L2 5'flanking sequence using BNCL2(mouse liver) cells, CV-1(African green monkey kidney) cells, HRP.1 trophoblasts and Drosophila Schneider(SL2) cells. Sequencing analysis was performed to find the region contained consensus binding sites for transcription factors. Standard gel shift(Electrophoretic mobility shift assay, EMSA) and supershift analysis using liver nuclear extracts was performed to establish proteins(transcription factors) bound this regulatory element. RESULTS: The 5'flanking region of the L2 untranslated region(UTR) exhibited promoter activity in BNCL2(mouse liver), CV-1(monkey kidney) cells and HRP.1 trophoblasts. Deletional analyses indicated the presence of a Sp binding site important for transcription of the L2 UTR and localized the major regulatory region within 75 bp of the 5'transcription start site. Sequencing analyses revealed the region contained consensus binding sites for the Sp family of transcription factors. EMSA and supershift EMSA revealed that in mouse liver nuclear extracts that Spl and Sp3 bound to this cis-element. Functional studies in Drosophila SL2 cells and BNCL2(mouse liver) cells established the ability of Sp3 and Sp1 to stimulate transcriptional activity via this cis-element. Functional studies in Drosophila SL2 cells demonstrated a functional interaction between Sp3 and Sp1 at this DNA-binding site. CONCLUSION: Sp family transcription factors play a role in regulation of L2 transcript gene expression in the 5'flanking region of the murine GHR gene.
Animals ; Binding Sites ; Cercopithecus aethiops ; Consensus ; Drosophila ; Electrophoretic Mobility Shift Assay ; Exons ; Gene Expression ; Growth Hormone* ; Humans ; Liver ; Metabolism ; Mice ; Receptors, Somatotropin* ; Regulatory Sequences, Nucleic Acid ; Transcription Factors* ; Transfection ; Trophoblasts

No abstract available.
Humans

To describe and evaluate the morphologic changes and the different expression of cell-specific or correlating protein molecules during cell growth, immunocytochemistry and morphologic observations were done on retinal pigment epithelial(RPE) cells obtained from several culture conditions. These include culture time, spatial or cell density, transdifferentiation, and presence of growth factors. The human fetal and porcine RPE cells were cultured with and without individual growth factor or in combinations inchlding extracellular matrix (ECM), Insulin, basic fibroblatio growth factor (bFGF) and epidermal growth factor (EGF). Mouse monoclonal anti-human, or anti-mouse antibodieg with or without species cross reactlvity against the intermediate filament proteins (cytokeratin, vimentin, GFAP) were used. To determine RPE-specific molecules of cytokeratin, nine commercially available antibodies, representing subclones of Moll's catalog number 1, 5, 7, 8, 10, 14, 17, 18, 19 were applied. The morphological changes and the proliferation of cells started after their attachment on the culture plate as soon as they lost pigment granules. The epithelial cells like fibroblasts occurred in the area where the cellular density was low, and finally, their shape was restored to their original phenotype when the cellular connuency was achieved. The degree of proliferation and the duration of achieving confluency of cells were dependent on whether ECM and growth factors were added in media or not. Cells with the epithelial morphology were positively stained with anticytokeratine antibodies, especially with clone 19, 18, 17, 8 and 7 in human RPE cells; with 19, CAM 5.26 (8/18) in porcine cells. The fusiform or digitating cells of sparse density also expressed vimentin strongly through out all stages, whereas GFAP was not expressed at any stage in either species.
Animals ; Antibodies ; Cell Count ; Clone Cells ; Epidermal Growth Factor ; Epithelial Cells* ; Extracellular Matrix ; Fibroblasts ; Humans ; Immunohistochemistry ; Insulin ; Intercellular Signaling Peptides and Proteins ; Intermediate Filament Proteins ; Keratins* ; Mice ; Phenotype ; Retinaldehyde* ; Vimentin*

PURPOSE: The purpose of the study was to identify the adequacy of enteral feeding, and the reason and prevalence of under-nutrition, and to determine the relationships between caloric intake and resulting nutritional parameters among neurosurgical intensive care unit (ICU) patients. METHODS: The participants for this descriptive study were 47 neurosurgical ICU patients who had enteral feeding initiated after ICU admission. Data were collected from the initial day of enteral feeding for 7 days. Data related to enteral feeding, feeding interruptions or delay, prealbumin, and transferrin were collected. RESULTS: The mean age of the participants was 56.62 years. Twenty-six patients did not receive their feeding formula more than once during 7 days, and 11 had interruptions more than 6 times. The mean number of feeding interruptions was 3.23 (SD= 4.47). On the average, only 76.44% of the estimated energy requirement was provided by enteral feeding to the patients. The frequency of underfeeding was 52.17% with respect to enteral feeding. The most frequent reason for the feeding interruption was observation before and after intubation and extubation, which was unavoidable. The next most common reason was gastrointestinal bleeding, mostly due to old clots or trace, followed by residual volume less than 100 mL. Changes in prealbumin and transferrin levels for 7 days between the underfed and adequately fed groups were not statistically significant. CONCLUSION: The management of enteral feeding by nurses was overprotective because of the unpredictable nature of ICU patients in terms of their underlying disease process. The management of feeding intolerance needs to be evidence-based and nurses must consistently follow the protocol that has been supported as a useful measure.
Energy Intake ; Enteral Nutrition ; Hemorrhage ; Humans ; Critical Care ; Intensive Care Units ; Intubation ; Malnutrition ; Neurosurgical Procedures ; Nutritional Support ; Prealbumin ; Prevalence ; Residual Volume ; Transferrin

To describe and evaluate the morphologic changes and the different expression of cell-specific or correlating protein molecules during cell growth, immunocytochemistry and morphologic observations were done on retinal pigment epithelial(RPE) cells obtained from several culture conditions. These include culture time, spatial or cell density, transdifferentiation, and presence of growth factors. The human fetal and porcine RPE cells were cultured with and without individual growth factor or in combinations inchlding extracellular matrix (ECM), Insulin, basic fibroblatio growth factor (bFGF) and epidermal growth factor (EGF). Mouse monoclonal anti-human, or anti-mouse antibodieg with or without species cross reactlvity against the intermediate filament proteins (cytokeratin, vimentin, GFAP) were used. To determine RPE-specific molecules of cytokeratin, nine commercially available antibodies, representing subclones of Moll's catalog number 1, 5, 7, 8, 10, 14, 17, 18, 19 were applied. The morphological changes and the proliferation of cells started after their attachment on the culture plate as soon as they lost pigment granules. The epithelial cells like fibroblasts occurred in the area where the cellular density was low, and finally, their shape was restored to their original phenotype when the cellular connuency was achieved. The degree of proliferation and the duration of achieving confluency of cells were dependent on whether ECM and growth factors were added in media or not. Cells with the epithelial morphology were positively stained with anticytokeratine antibodies, especially with clone 19, 18, 17, 8 and 7 in human RPE cells; with 19, CAM 5.26 (8/18) in porcine cells. The fusiform or digitating cells of sparse density also expressed vimentin strongly through out all stages, whereas GFAP was not expressed at any stage in either species.
Animals ; Antibodies ; Cell Count ; Clone Cells ; Epidermal Growth Factor ; Epithelial Cells* ; Extracellular Matrix ; Fibroblasts ; Humans ; Immunohistochemistry ; Insulin ; Intercellular Signaling Peptides and Proteins ; Intermediate Filament Proteins ; Keratins* ; Mice ; Phenotype ; Retinaldehyde* ; Vimentin*

No abstract available.
Hamartoma*

No abstract available.

Infantile hemangioendothelioma of the liver is a common vascular tumor in infancy. The tumor is usually multinodular or diffuse and classified into two types. We present a case of infantile hemangioendothelioma of the liver, which predominantly consists of type 2. A 4-month-old female was admitted for an evaulation of an abdominal distension. A CT scan of the liver showed a multinodular mass. The right lobectomy was done. Grossly, the mass consisted of round nodules ranging from 2cm to 5cm in diameter. Microscopically, the tumor revealed proliferation of small vascular channels lined by endothelial cells. Bizarre cells and mitotic cells were frequently noted. Vesicular nuclei and multilayering of the endothelial cells were also noted.
Endothelial Cells ; Female ; Hemangioendothelioma* ; Humans ; Infant ; Liver* ; Tomography, X-Ray Computed