1.Alterations of erythrocyte deformability and membrane protein after high intensity training and recovery in rats.
Ping HONG ; Kai-Gang LI ; Lian-Shi FENG
Chinese Journal of Applied Physiology 2002;18(3):269-273
AIM AND METHODSThe purpose of this investigation was to determine the changes of erythrocyte deformability, band-3 protein and actin in the definite volume of erythrocyte membrane after high intensity running training and recovery in rats.
RESULTSLong-term training could significantly improve erythrocyte deformability and the quantity of membrane proteins. Erythrocyte deformability, band-3 protein and actin decreased transitorily at varying degrees after inadaptable high intensity exercise. One and two week training could improve erythrocyte deformability, the quantity of band-3 protein and actin after recovery.
CONCLUSIONAlterations of erythrocyte membrane protein after high intensity training could cause the change in erythrocyte membrane structure and hence influenced erythrocyte deformability. That was maybe one of mechanisms of training effecting erythrocyte deformability.
Actins ; metabolism ; Animals ; Anion Exchange Protein 1, Erythrocyte ; metabolism ; Erythrocyte Deformability ; Erythrocyte Indices ; Erythrocyte Membrane ; chemistry ; metabolism ; Physical Conditioning, Animal ; Rats ; Rats, Sprague-Dawley
2.Changes of protein tyrosine phosphorylation in erythrocyte band 3 glucose-6-phosphate dehydrogenase deficiency.
Guoyu YU ; Jialin LI ; Xingya TIAN ; Hong LIN ; Xiaoying WANG
Chinese Journal of Hematology 2002;23(11):565-567
OBJECTIVETo explore the hemolytic mechanism of glucose-6-phosphate dehydrogenase (G6PD) deficient erythrocytes in the view of phosphorylation of membrane protein.
METHODSThe alternation of membrane protein phosphorylation and the effect of dithiothreitol (DTT) on protein phosphorylation were analysed by Western blot technique. The activity of phosphotyrosine phosphatase (PTPs) was determined by using p-nitrophenyl phosphate as substrate.
RESULTSTyrosine phosphorylation of band 3 protein was obviously enhanced in G6PD-deficient erythrocytes. The activity of PTPs was low compared to the normal erythrocytes. The level of phosphotyrosine in G6PD-deficient erythrocytes incubated with DTT was almost the same as in those without DTT. The results were consistent with the activity of PTPs.
CONCLUSIONSPTPs activity reduction and tyrosine phosphorylation enhancement induced by oxidation in G6PD deficiency play an important role in erythrocytes hemolysis. However, the alternation of thiol group is not the only factor affecting the activity of PTPs in G6PD-deficient erythrocytes.
Anion Exchange Protein 1, Erythrocyte ; metabolism ; Blotting, Western ; Erythrocyte Membrane ; metabolism ; Glucosephosphate Dehydrogenase Deficiency ; enzymology ; metabolism ; Humans ; Phosphorylation ; Protein Tyrosine Phosphatases ; metabolism ; Tyrosine ; metabolism
3.Basicranial sellar tumor.
Chinese Journal of Pathology 2009;38(7):483-484
Anion Exchange Protein 1, Erythrocyte
;
metabolism
;
Antiporters
;
metabolism
;
Child
;
Chordoma
;
metabolism
;
pathology
;
radiotherapy
;
surgery
;
Female
;
Follow-Up Studies
;
Humans
;
Skull Base Neoplasms
;
metabolism
;
pathology
;
radiotherapy
;
surgery
;
Vimentin
;
metabolism
4.Microglandular adenosis of breast: report of a case.
Gui-mei QU ; Zhi-qiang LANG ; Wei-dong YAO ; Guo-hua YU ; Wen-fang YU
Chinese Journal of Pathology 2007;36(9):643-644
5.Ectopic hamartomatous thymoma: a clinicopathological and immunohistochemical study of two cases.
Chinese Journal of Pathology 2005;34(7):397-401
OBJECTIVETo study the clinicopathological and immunohistochemical features of ectopic hamartomatous thymoma (EHT), and to discuss its histogenesis.
METHODSThe clinical and pathologic features of two EHT cases of were evaluated. Immunohistochemical study was performed by LSAB method using a panel of antibodies including AE1/AE3, CK5, CK7, CK8, CK20, EMA, vimentin, CD5, CD10, alpha-SMA, calponin, desmin, CD34, S-100 protein, CD57, GFAP, TTF-1 and CD99.
RESULTSBoth cases occurred in males aged 20 years and 40 years respectively. Each patient presented with a solitary mass, one located in the suprasternal fossa and the other in the left supraclavicular region for a period of 6 months and 2 months respectively. Grossly, the masses were well-circumscribed with spherical and ovoid appearance, measuring 5 cm and 3 cm in maximum diameter respectively. On cut section, they were gray-white in color and of soft consistency. Histologically, both tumors were composed of a mixture of spindle cells, epithelial cells and mature adipose tissue. The spindle cells element accounted 85% and 70% each in the two cases. They resembled fibroblasts in morphology and were arranged frequently in fascicular, woven or storiform patterns. Epithelial cells element represented nearly 10% in both cases. Most of the epithelial cells had a non-keratinization squamous appearance. They formed small solid islands and adamantinoma-like "nastomosing cords", or appeared as lining cells in large cystic spaces. In focal areas, glandular differentiation presented as small glands. A transition between the spindle cell and epithelium components could be also identified in some areas. Mature adipose tissue was irregularly distributed in the two tumors, about < 5% and 20% respectively. Immunohistochemically, the epithelial element expressed AE1/AE3, CK5, CK7, CK8 and EMA, whereas the spindle component expressed AE1/AE3, CK5, CK7, CK8, vimentin, CD10, CD34, alpha-SMA, MSA, and calponin. Both elements were negative for CK20, TTF-1, desmin, S-100 protein, CD57, GFAP and CD99.
CONCLUSIONSEHT is a benign tumor that occurs predominantly in the lower neck region of young to middle-aged males. Immunohistochemical study revealed myoepithelial differentiation of the spindle cells, suggesting EHT is a mixed tumor composed of epithelial and myoepithelial cells. EHT possibly originates from the remnants of cervical sinus of His, and therefore, may be renamed as branchial anlage mixed tumor.
Adult ; Anion Exchange Protein 1, Erythrocyte ; metabolism ; Choristoma ; metabolism ; pathology ; surgery ; Diagnosis, Differential ; Hamartoma ; Humans ; Keratins, Type II ; metabolism ; Lymphatic Diseases ; metabolism ; pathology ; surgery ; Male ; Mucin-1 ; metabolism ; Thymoma ; metabolism ; pathology ; surgery ; Thymus Neoplasms ; metabolism ; pathology ; surgery ; Vimentin ; metabolism
6.Clinicopathologic and immunohistochemical study of pulmonary epithelioid hemangioendothelioma.
Rui-e FENG ; Hong-rui LIU ; Tong-hua LIU
Chinese Journal of Pathology 2005;34(1):33-35
OBJECTIVETo study the clinical and pathological characteristics of pulmonary epithelioid hemangioendothelioma.
METHODSFour cases of pulmonary epithelioid hemangioendothelioma were studied by histopathologic and immunohistochemical examination of lung biopsy specimens.
RESULTSThere were 3 female and 1 male, age 28 to 40 years. Clinically the tumor presented as multiple bilateral small nodules in the lung. Histologically, crown-like clusters of epithelioid tumor cells were obtained which filled in the alveoli locating at the periphery of the tumor nodules, while the central part of the nodules contained myxoid to hyaline matrix. The overall architecture of the lung was still preserved. Additionally, intracytoplasmic vacuoles were seen in tumor cells within which red blood cells were sometimes identified. Tumor cells generally lacked pleomorphism, mitotic activity and necrosis. They were immunohistochemically positive for CD31 and CD34. AE1/AE3 staining was positive in some cases.
CONCLUSIONSPulmonary epithelioid hemangioendothelioma often occurs in a middle-aged woman and represents a distinct clinical pathological entity.
Adult ; Anion Exchange Protein 1, Erythrocyte ; analysis ; Antigens, CD34 ; analysis ; Antiporters ; analysis ; Female ; Hemangioendothelioma, Epithelioid ; immunology ; metabolism ; pathology ; Humans ; Immunohistochemistry ; Lung ; pathology ; Lung Neoplasms ; immunology ; metabolism ; pathology ; Male ; Platelet Endothelial Cell Adhesion Molecule-1 ; analysis
7.Immunolocalization of anion exchanger 1 (Band 3) in the renal collecting duct of the common marmoset.
Ji Hyun SONG ; Yong Hwan KIM ; Tae Cheon KANG ; Moo Ho WON ; Jun Gyo SUH ; Byung Hwa HYUN ; Yang Seok OH ; Si Yun RYU ; Ju Young JUNG
Journal of Veterinary Science 2007;8(4):329-333
The purpose of this study was to determine the expression and distribution of band 3 in the collecting duct and connecting tubules of the kidney of the marmoset monkey (Callithrix jacchus), and to establish whether band 3 is expressed in type A intercalated cells. The intracellular localization of band 3 in the different populations of intercalated cells was determined by double-labeling immunohistochemistry. Immunohistochemical microscopy demonstrated that band 3 is located in the basolateral plasma membranes of all type A intercalated cells in the connecting tubule (CNT), cortical collecting duct (CCD), and outer medullary collecting duct (OMCD) of the marmoset. However, type B intercalated cells and non-A/ non-B intercalated cells did not show band 3 labeling. Electron microscopy of the CNT, CCD and OMCD confirmed the light microscopic observation of the basolateral plasma membrane staining for band 3 in a subpopulation of interacted cells. Basolateral staining was seen on the plasma membrane and small coated vesicles in the perinuclear structure, some of which were located in the Golgi region. In addition, there was no labeling of band 3 in the mitochondria of the CNT, CCD and in OMCD cells. The intensity of the immunostaining of the basolateral membrane was less in the CNT than in the CCD and OMCD. In contrast, band 3 immunoreactivity was greater in the intracellular vesicles of the CNT. From these results, we suggest that the basolateral Cl-/HCO3- exchanger in the monkey kidney is in a more active state in the collecting duct than in the CNT.
Animals
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Anion Exchange Protein 1, Erythrocyte/*metabolism
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Callithrix/*metabolism
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Gene Expression Profiling/veterinary
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*Gene Expression Regulation
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Immunohistochemistry/veterinary
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Kidney Tubules/cytology/physiology/ultrastructure
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Kidney Tubules, Collecting/cytology/*metabolism/ultrastructure
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Male
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Microscopy, Electron, Transmission/veterinary
8.Inflammatory myofibroblastic tumor of bladder: a clinicopathologic study of five cases.
Ke SUN ; Zhao-ming WANG ; Lin-jie XU ; Xiao-dong TENG ; Hong-tian YAO ; Guo-ping REN
Chinese Journal of Pathology 2007;36(9):605-608
OBJECTIVETo study the clinicopathologic features, diagnosis and differential diagnosis of inflammatory myofibroblastic tumor of the urinary bladder.
METHODSExcisional specimens from 5 cases of vesical inflammatory myofibroblastic tumor were studied by light microscopy and immunohistochemistry (EnVision). The clinical data were also analyzed.
RESULTSAmong the 5 patients studied, 3 were males and 2 were females. The age of the patients ranged from 10 to 53 years (mean age = 35 years). The most common clinical presentation was micturition pain and hematuria. Three cases were located at the dome of the urinary bladder and the remaining 2 cases were found in the left lateral wall. Histologically, the tumor varied from myxoid to highly cellular. The tumor cells were spindle to stellate in shape, widely separated or showed a compact fascicular pattern. There were often associated with mixed inflammatory infiltrates and an irregular meshwork of small dilated vessels. Immunohistochemical study showed that the tumor cells expressed AE1/AE3 (5/5), vimentin (5/5), smooth muscle actin (5/5), calponin (5/5), caldesmon (3/5), desmin (4/5) and anaplastic lymphoma kinase protein (4/5). Follow-up data were available in 4 patients and none had local recurrence or died of this disease.
CONCLUSIONInflammatory myofibroblastic tumour of urinary bladder is a rarely encountered but distinctive neoplasm with intermediate malignant potential.
Actins ; metabolism ; Adolescent ; Anion Exchange Protein 1, Erythrocyte ; metabolism ; Calcium-Binding Proteins ; metabolism ; Child ; Cystectomy ; methods ; Diagnosis, Differential ; Female ; Fibrosarcoma ; pathology ; Follow-Up Studies ; Humans ; Inflammation ; pathology ; Leiomyosarcoma ; pathology ; Male ; Microfilament Proteins ; metabolism ; Middle Aged ; Neoplasms, Muscle Tissue ; metabolism ; pathology ; surgery ; Protein-Tyrosine Kinases ; metabolism ; Receptor Protein-Tyrosine Kinases ; Rhabdomyosarcoma ; pathology ; Survival Rate ; Urinary Bladder Neoplasms ; metabolism ; pathology ; surgery ; Vimentin ; metabolism
9.Renal medullary carcinoma in child: report of a case.
Li CAI ; Gui-mei QU ; Hou-cai LIU
Chinese Journal of Pathology 2009;38(7):486-487
Anion Exchange Protein 1, Erythrocyte
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metabolism
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Biomarkers
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metabolism
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Carcinoembryonic Antigen
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metabolism
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Carcinoma, Medullary
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metabolism
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pathology
;
surgery
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Carcinoma, Transitional Cell
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metabolism
;
pathology
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Child
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Diagnosis, Differential
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Female
;
Humans
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Keratins
;
metabolism
;
Kidney Neoplasms
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metabolism
;
pathology
;
surgery
;
Kidney Tubules, Collecting
;
pathology
;
Mucin-1
;
metabolism
;
Nephrectomy
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Rhabdoid Tumor
;
metabolism
;
pathology
;
Vimentin
;
metabolism
10.Study on the effects of two kinds of cactus polysaccharide on erythrocyte membrane protein and fluidity of the lipid in S180 mice.
Yu-bin JI ; Chen-feng JI ; Xiang ZOU ; Shi-yong GAO
China Journal of Chinese Materia Medica 2004;29(10):967-970
OBJECTIVETo study the effects of two kinds of cactus polysaccharide on Band 3 protein, cross-linking protein and lipid fluidity of erythrocyte membrane in S180 mice.
METHODThe membrane protein content was analysed by SDS-PAGE. Lipid fluidity was measured by Skinitzky method.
RESULTThe two kinds of cactus polysaccharide increased the content of Band 3 protein and decreased the content of cross-linking protein, raised the lipid fluidity. While the effect of median dose group of medical cactus polysaccharide is very remarkable (P < 0.01), the effect of high dose group of edible cactus polysaccharide is very remarkable (P < 0.01).
CONCLUSIONBy improving the erythrocyte membrane function of tumor-mice, they enhanced the immune function, which may be one of anti-tumor mechanisms.
Animals ; Anion Exchange Protein 1, Erythrocyte ; metabolism ; Antineoplastic Agents, Phytogenic ; administration & dosage ; isolation & purification ; pharmacology ; Dose-Response Relationship, Drug ; Erythrocyte Membrane ; metabolism ; physiology ; Male ; Membrane Fluidity ; drug effects ; Mice ; Opuntia ; chemistry ; Plants, Medicinal ; chemistry ; Polysaccharides ; administration & dosage ; isolation & purification ; pharmacology ; Sarcoma 180 ; metabolism