1.Biliary Hamartoma.
The Korean Journal of Hepatology 2003;9(2):151-152
No abstract available.
Cytoskeleton/*ultrastructure
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Hepatocytes/*ultrastructure
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Humans
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Liver Diseases/*pathology
2.Analysis of the common morphological characteristics of cancerous cells using atomic force microscope.
Qing-ming SHU ; Yue-yue LI ; Ming ZHU ; Xin-wu ZHANG ; Xiao-dong WANG ; Hui CHEN ; Xiao-long JI
Journal of Southern Medical University 2011;31(2):205-209
OBJECTIVETo observe the surface ultrastructure of different tumor cells in vivo using atomic force microscope (AFM) and analyze their common characteristics.
METHODSWe selected 60 specimens of each of normal liver cells, liver cancer, cervical squamous cells, cervical cancer cells, ductal epithelial cells and breast cancer cells for scanning using AFM. The cell surface scan images were analyzed using image analysis software to identify their common morphological features.
RESULTSFrom normal cervical squamous epithelial cells, intermediate cells, and basal cells to HPV-infected cells, CIN2-3 cells and cervical cancer cells, the membrane surface roughness became gradually increased (P<0.05). Similarly, the surface roughness increased significantly in the order of normal liver cells, hepatitis B cirrhosis liver cells, and hepatocellular carcinoma cells (P<0.05). The average surface roughness also tended to increase from normal mammary gland cells to mammary gland hyperplasia cells and breast cancer cells (P<0.05).
CONCLUSIONNormal cells and tumor cells show different cell membrane morphologies, and such morphological features provide a reliable basis for clinical pathological diagnosis and differential diagnosis of malignancies.
Breast Neoplasms ; ultrastructure ; Epithelial Cells ; ultrastructure ; Female ; Hepatocytes ; ultrastructure ; Humans ; Image Processing, Computer-Assisted ; Liver Neoplasms ; ultrastructure ; Male ; Membrane Proteins ; ultrastructure ; Microscopy, Atomic Force ; Uterine Cervical Neoplasms ; ultrastructure
3.Ultrastructure of Chronic Liver Diseases: Mallory Body of the Hepatocyte.
The Korean Journal of Hepatology 2003;9(1):49-66
No abstract available.
Chronic Disease
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Hepatocytes/*ultrastructure
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Humans
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Inclusion Bodies/*ultrastructure
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Liver Diseases/*pathology
4.Ultrastructural changes of hepatocyte fibrogenesis in cholelithiasis.
Ming YE ; Pin TU ; Gui-mei LI ; Mei-zhao LE ; Mao-hong ZHANG
Chinese Journal of Hepatology 2010;18(12):924-926
OBJECTIVETo explore the ultrastructural changes of hepatocyte fibrogenesis in cholelithiasis in biliary tract.
METHODSl0 liver biopsies were taken from the patients suffered from gallstone and choledocholithiasis during surgical treatment and the ultrastructural changes were observed under electromicroscope.
RESULTSThere were plentiful collagenous microfibrils (CMFs) grown within some hepatocytes. These CMFs distributed locally or diffusely in cytoplasm even extended into nucleus. In 7 cases numerous megamitochondrias appeared in several hepatocytes, the inclusions mimicking fibrils could be frequently seen and grew beyond the envelope. Furthermore, typical CMFs could be seen in the large microbodies, and several vesicular or cystic structures similar as fibroblast were presented in marginal areas of the hepatocytes.
CONCLUSIONSWe deduce that the fibrosed hepatocytes may be remained and take part in the hyperplasia of hepatic fibrous tissue.
Adult ; Cholelithiasis ; pathology ; ultrastructure ; Female ; Hepatocytes ; pathology ; ultrastructure ; Humans ; Liver Cirrhosis ; pathology ; Male ; Middle Aged
5.Increased Microfilaments in Hepatocytes and Biliary Ductular Cells in Cholestatic Liver Diseases.
Kyu Won CHUNG ; Nam Ik HAN ; Sang Wook CHOI ; Byung Min AHN ; Seung Kyu YOON ; Soon Woo NAM ; Young Sok LEE ; Jun Yeol HAN ; Hee Sik SUN
Journal of Korean Medical Science 2002;17(6):795-800
To assess the extent of microfilaments in cholestatic liver diseases we examined the cytoplasmic microfilaments in intrahepatic and extrahepatic cholestasis in man by electron microscopy. Study subjects were two patients with drug-induced intrahepatic cholestasis, three patients with intrahepatic cholestasis due to viral hepatitis, four patients with extrahepatic cholestasis due to stones of the common bile duct and two patients with primary biliary cirrhosis. Two biopsied specimens from patients without clinical or histological evidence of liver disease served as noncholestatic controls. The microfilaments in hepatocytes and biliary ductular cells were significantly increased in cholestasis compared with those in non-cholestatic controls. Well developed bundles of microfilaments were noted around the pericanalicular ectoplasm and seemed to be parallel to plasma membrane of the hepatocytes in cholestasis. In cholestasis, there were increased bundles of microfilaments around the periluminal region, lateral cell wall, and nucleus of biliary ductular cells. Two patterns of microfilaments bundles (fine microfilamentous network and spindle-shaped dense or clusters of microfilaments) were associated with cholestasis. The clustered form of microfilaments also seemed to be clearly associated with intracytoplasmic vacuoles containing bile salts. In conclusion, the increase of microfilaments in hepatocytes and biliary ductular cells may be the consequence of various forms of cholestasis. Further studies are needed to clarify the functional significance of increased microfilaments in cholestasis.
Bile Canaliculi/*pathology/ultrastructure
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Biopsy
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Cholestasis, Intrahepatic/*pathology
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Hepatocytes/*pathology/ultrastructure
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Humans
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Microfilaments/*pathology/ultrastructure
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Microscopy, Electron
6.Effect of yeast RNA on physical functions, morphology of hepatic cells and brain neurons in aged rats.
Hong-zhi PAN ; Xin ZHAO ; Wen-feng CHU ; Rong LI
Chinese Journal of Preventive Medicine 2003;37(3):158-160
OBJECTIVETo study the effect of exogenous nucleic acid on physical functions, morphology of hepatic cells and brain neurons in aged rats.
METHODSThirty two aged Wistar rats (20 month-old) were divided randomly into four groups (one aged control group and three aged experimental groups) and eight young rats (3 month-old) was set as young control group. Control groups were fed on standard chow and experimental groups were fed on standard chow supplemented with 93.75 mg/kg (high-dosage group), 46.88 mg/kg (middle-dosage group) and 9.38 mg/kg (low-dosage group) of yeast RNA respectively. SOD, MDA, HDL, sex hormone and growth hormone were determined at the end of a 4-week observation. The microcosmic images of the hepatic cells and brain neurons using the image-pro plus (V.4.0) were also observed.
RESULTSSOD, serum HDL and growth hormone levels in the high dosage group were significantly higher (P < 0.05) than that in the aged control group, and the levels were not different from that in the young control group. MDA level of all yeast RNA supplemented groups was significantly lower than that of aged control group (P < 0.05) and that was not different from the young control group. Serum testosterone of the high and middle dosage groups reached the level of young control group, and that was much higher than the aged control and low dosage group (P < 0.05). Estradiol levels among the aged rats were not different, and those were much lower than the young control group (P < 0.05). Much more number of brain neurons were observed in the high-dose group than other aged rats (P < 0.05). Brain neurons, hepatic cells and karyons in the high-dose group were bigger than that in other aged rats (P < 0.05).
CONCLUSIONExogenous yeast RNA might play an important role in physical functions, the morphology of brain neurons and hepatic cells in natural aged rats. There might have a dose-effect relationship in the process.
Aging ; Animals ; Brain ; physiology ; ultrastructure ; Dose-Response Relationship, Drug ; Hepatocytes ; ultrastructure ; Liver ; physiology ; ultrastructure ; Male ; Neurons ; ultrastructure ; RNA, Fungal ; pharmacology ; Random Allocation ; Rats ; Rats, Wistar ; Yeasts ; chemistry
8.Ultracytochemical observation of the intracellular localization of H+-adenosine triphosphatase.
Shen-qiu LUO ; Zhi-yong KE ; Yan-meng LU
Journal of Southern Medical University 2011;31(8):1431-1433
OBJECTIVETo observe the ultracytochemical localization of H(+)-adenosine triphosphatase (H(+)-ATPase) in the cell organelles.
METHODSThe localization of H(+)-ATPase in the cell organelles was observed in the hepatocytes and renal cells of Wistar rats using routine ultracytochemical methods.
RESULTSH(+)-ATPase activities were observed on the lysosomal membrane and nuclear envelope of the hepatocytes and proximal tubule epithelial cells of the nephron in Wistar rats.
CONCLUSIONThis finding supports the hypothesis that H(+)-ATPase (V-ATPase) is present on the plasma membrane and in the endomembrane system.
Animals ; Cell Membrane ; enzymology ; Hepatocytes ; cytology ; enzymology ; ultrastructure ; Histocytochemistry ; methods ; Kidney ; cytology ; enzymology ; ultrastructure ; Lysosomes ; enzymology ; Male ; Organelles ; enzymology ; Rats ; Rats, Wistar ; Vacuolar Proton-Translocating ATPases ; metabolism
9.Preparation of galactosylated hyaluronic acid/chitosan scaffold for liver tissue engineering.
Jinyong FAN ; Yi SHANG ; Jun YANG ; Yingjin YUAN
Journal of Biomedical Engineering 2009;26(6):1271-1275
The purpose of this research is to construct a kind of 3D-Scaffold with galactose-carrying polysaccharide for improving the function of hepatocytes in vitro. Galactose moieties were covalently coupled with hyaluronic acid through ethylenediamine. Galactosylated hyaluronic acid/chitosan scaffolds were prepared by lyophilization. The characteristics of the scaffolds such as morphology, hydrophilicity, and mechanical properties were investigated. The results indicated that the porosity and the pore size of the scaffolds made in -20 degrees C were useful used for culturing hepatocytes. And, the incorporating of hyaluronic acid in chitosan network improved the hydrophilicity and mechanical properties of the scaffolds. Rat primary hepatocytes growing in the scaffolds observed by phase-contrast microscope showed the multicellular spheroid morphologies. Therefore, galactosylated hyaluronic acid/chitosan scaffolds could be used as a promising scaffold for liver tissue engineering.
Animals
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Cells, Cultured
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Chitosan
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chemistry
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pharmacology
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Galactose
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chemistry
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pharmacology
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Hepatocytes
;
physiology
;
ultrastructure
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Hyaluronic Acid
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chemistry
;
pharmacology
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Liver
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physiology
;
ultrastructure
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Porosity
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Rats
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Tissue Engineering
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Tissue Scaffolds
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chemistry
10.Pleomorphism of the myelin-like bodies in the hepatocytes of patients with Dubin-Johnson syndrome complicated with chronic hepatitis B.
Xiao-Bo LU ; Hao LIU ; Qin XU ; Yue-Xin ZHANG ; Ze-Run DENG ; An-Hua HU ; Wen-Jie LIU ; Rong-Fu LV
Chinese Journal of Hepatology 2011;19(3):210-213
OBJECTIVETo explore characteristics of the myelin-like bodies in the hepatocytes of patients with Dubin-Johnson syndrome (DJS) complicated with chronic hepatitis B (CHB).
METHODS11 cases of DJS complicated with CHB and 5 cases DJS without CHB were studied clinicopathologically. The hepatocyte ultrastructure was observed with transmission electron microscope and taken photos. The data were compared and analyzed using Fisher's Exact Test.
RESULTSDeposition of myelin-like bodies can be observed in the hepatocytes of DJS patients with CHB but can not in DJS patients without CHB. The morphology of pigment varys. The electron density and volume of pigment in DJS patients with CHB can be classified into five types: brights (2/11,18.2%), reticulation (1/11, 9.1%), punctiform (6/11, 54.5%), abnormity (1/11, 9.1%) and primary type (1/11, 9.1%). The myelin-like bodies in the hepatocytes of patients with DJS are high density and round with membrance (we named it as primary type) (5/5, 100%).
CONCLUSIONSThe myelin-like bodies in the hepatocytes of DJS patients with CHB possess special pleomorphism and may have important diagnostic value.
Adolescent ; Adult ; Female ; Hepatitis B, Chronic ; complications ; pathology ; Hepatocytes ; chemistry ; pathology ; ultrastructure ; Humans ; Jaundice, Chronic Idiopathic ; complications ; pathology ; Male ; Myelin Sheath ; ultrastructure ; Young Adult