1.Epididymosomes are involved in the acquisition of new sperm proteins during epididymal transit.
Robert SULLIVAN ; Gilles FRENETTE ; Julie GIROUARD
Asian Journal of Andrology 2007;9(4):483-491
During epididymal transit, spermatozoa acquire new proteins. Some of these newly acquired proteins behave as integral membrane proteins, including glycosylphosphatidylinositol (GPI)-anchored proteins. This suggests that the secreted epididymal proteins are transferred to spermatozoa by an unusual mechanism. Within the epididymal lumen, spermatozoa interact with small membranous vesicles named epididymosomes. Many proteins are associated with epididymosomes and the protein composition of these vesicles varies along the excurrent duct and differs from soluble intraluminal proteins. Some epididymosome-associated proteins have been identified and their functions in sperm maturation hypothesized. These include P25b, a zona pellucida binding protein, macrophage migration inhibitory factor, enzymes of the polyol pathway, HE5/CD52, type 5 glutathione peroxidase, and SPAM1 or PH-20. The electrophoretic patterns of proteins associated to epididymosomes are complex and some of these proteins are transferred to defined surface domains of epididymal spermatozoa. Epididymosomes collected from different epididymal segments interact differently with spermatozoa. This protein transfer from epididymosomes to spermatozoa is time-dependent, temperature-dependent and pH-dependent, and is more efficient in the presence of zinc. Some proteins are segregated to lipid raft domains of epididymosomes and are selectively transferred to raft domains of the sperm plasma membrane. Some evidence is presented showing that epididymosomes are secreted in an apocrine manner by the epididymal epithelial cells. In conclusion, epididymosomes are small membranous vesicles secreted in an apocrine manner in the intraluminal compartment of the epididymis and play a major role in the acquisition of new proteins by the maturing spermatozoa.
Animals
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Antigens, Surface
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physiology
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Epididymis
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physiology
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Epithelial Cells
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physiology
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Humans
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Male
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Mice
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Proteins
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metabolism
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Sperm Motility
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physiology
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Spermatozoa
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physiology
2.The Role of Mesothelial Cells in Liver Development, Injury, and Regeneration.
Gut and Liver 2016;10(2):166-176
Mesothelial cells (MCs) cover the surface of visceral organs and the parietal walls of cavities, and they synthesize lubricating fluids to create a slippery surface that facilitates movement between organs without friction. Recent studies have indicated that MCs play active roles in liver development, fibrosis, and regeneration. During liver development, the mesoderm produces MCs that form a single epithelial layer of the mesothelium. MCs exhibit an intermediate phenotype between epithelial cells and mesenchymal cells. Lineage tracing studies have indicated that during liver development, MCs act as mesenchymal progenitor cells that produce hepatic stellate cells, fibroblasts around blood vessels, and smooth muscle cells. Upon liver injury, MCs migrate inward from the liver surface and produce hepatic stellate cells or myofibroblast depending on the etiology, suggesting that MCs are the source of myofibroblasts in capsular fibrosis. Similar to the activation of hepatic stellate cells, transforming growth factor β induces the conversion of MCs into myofibroblasts. Further elucidation of the biological and molecular changes involved in MC activation and fibrogenesis will contribute to the development of novel approaches for the prevention and therapy of liver fibrosis.
Epithelial Cells/*physiology
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Epithelium/metabolism
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Hepatic Stellate Cells/*physiology
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Humans
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Liver/*cytology/injuries/*physiology
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Liver Cirrhosis/etiology/prevention & control
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Liver Regeneration/*physiology
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Mesenchymal Stromal Cells/physiology
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Myofibroblasts/physiology
3.Repair, survival and apoptosis of type II alveolar epithelial cells and the change of bcl-2/p53 in oxidative stress.
Jing JIANG ; Feng XU ; Juan CHEN
Chinese Journal of Pediatrics 2008;46(1):74-75
Alveolar Epithelial Cells
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metabolism
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pathology
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Animals
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Apoptosis
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physiology
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Cell Survival
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physiology
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Cells, Cultured
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Epithelial Cells
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cytology
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physiology
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Genes, bcl-2
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genetics
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Genes, p53
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genetics
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Oxidative Stress
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genetics
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Rats
4.Cell adhesion molecules in human embryo implantation.
Michiko N FUKUDA ; Kazuhiro SUGIHARA
Acta Physiologica Sinica 2012;64(3):247-258
The process of human embryo implantation is mediated not only by evolutionarily conserved mechanisms, but also by a mechanism unique to humans. Evidence suggests that the cell adhesion molecules, L-selectin and trophinin, play a unique role in human embryo implantation. Here, we describe the dual roles of mucin carbohydrate ligand for L-selectin and trophinin protein and of the trophinin-associated proteins bystin and tastin. We then describe trophinin-mediated signal transduction in trophectoderm cells and endometrial epithelial cells. This review also covers cadherin and integrin in human embryo implantation.
Cadherins
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physiology
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Cell Adhesion Molecules
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physiology
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Embryo Implantation
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Epithelial Cells
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metabolism
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Humans
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Integrins
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physiology
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L-Selectin
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physiology
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Signal Transduction
5.Biological effect of inhibition of Notch signaling pathway on human dental pulp cells.
Xiaoying ZOU ; Heng ZHUANG ; Lin YUE ; Xuejun GAO
Chinese Journal of Stomatology 2014;49(4):210-215
OBJECTIVETo investigate the effect of Notch signaling pathway on human dental pulp cells.
METHODSThe γ-secretase inhibitor N-[N-(3, 5-difluorophenacetyl-L-alanyl)]-S-phenylglycine t-butyl ester(DAPT) was applied to inhibit the Notch signaling pathway of human dental pulp cells. The solvent dimethly sulfoxide (DMSO) served as the negative control.Senescence conditions were evaluated by cells morphology changes, the alkaline phosphatase (ALP) expression and its activity, senescence-associated β-galactosidase (SA-β-Gal) expression and the senescence related gene p53 expression.
RESULTSAfter inhibition of the Notch signaling pathway, morphology changes, including flatter cells, larger plasma area, were seen in the 10th passage human dental pulp cells. ALP expression and activity showed a significant decrease at the 8th passage after inhibition (35.36 ± 2.55) U/g, compared with the negative control group[(49.76 ± 4.30) U/g] (t = 4.989, P = 0.008).SA-β-Gal-positive cells could be seen as early as the 8th passage and more positive cells were evident at the 10th passage. The relative expression level of p53 gene was elevated in the 10th passage cells (1.7 ± 0.4) compared with the negative control group(1.0) (t = 3.581, P = 0.012).
CONCLUSIONSHuman dental pulp cells became senescent at earlier passages after inhibition of Notch signaling pathway.Notch signaling pathway may affect life cycle of human dental pulp cells.
Cells, Cultured ; Dental Pulp ; metabolism ; Epithelial Cells ; Humans ; Receptors, Notch ; physiology ; Signal Transduction
6.Vesicular transport as a new paradigm in short-term regulation of transepithelial transport.
Chun Sik PARK ; Chae Hun LEEM ; Yeon Jin JANG ; Yhong Hee SHIM
Journal of Korean Medical Science 2000;15(2):123-132
The vectorial transepithelial transport of water and electrolytes in the renal epithelium is achieved by the polarized distribution of various transport proteins in the apical and basolateral membrane. The short-term regulation of transepithelial transport has been traditionally thought to be mediated by kinetic alterations of transporter without changing the number of transporters. However, a growing body of recent evidence supports the possibility that the stimulus-dependent recycling of transporter-carrying vesicles can alter the abundance of transporters in the plasma membrane in parallel changes in transepithelial transport functions. The abundance of transporters in the plasma membrane is determined by net balance between stimulus-dependent exocytic insertion of transporters into and endocytic retrieval of them from the plasma membrane. The vesicular recycling occurs along the tracts of the actin microfilaments and microtubules with associated motors. This review is to highlight the importance of vesicular transport in the short-term regulatory process of transepithelial transport in the renal epithelium. In the short-term regulation of many other renal transporters, vesicular transport is likely to be also involved. Thus, vesicular transport is now emerged as a wide-spread general regulatory mechanism involved in short-term regulation of renal functions.
Animal
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Biological Transport/physiology
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Endocytosis/physiology*
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Epithelial Cells/enzymology*
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Epithelial Cells/cytology*
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Exocytosis/physiol(HCMV)*
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H(+)-Transporting ATP Synthase/metabolism*
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Human
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Sodium Channels/metabolism
7.The TGF-β signaling pathway induced EMT in breast cancer.
Yan MA ; Hong LIU ; Hao ZHANG ; Rong-guang SHAO
Acta Pharmaceutica Sinica 2015;50(4):385-392
Epithelial-mesenchymal transition (EMT) refers to tne transition during which epithelial cells undergo the loss of apical-basal polarity, acquisition of migration capability and transformation into mesenchymal cells. EMT induces breast cancer in situ to developing into metastasis and associates with the drug resistence. The multiple elements including signal pathways, transcriptional factors and downstream genes orchestrate the transition. Among them, the transforming growth factor β (TGF-β) signaling pathway plays a key role in the regulation of EMT in breast cancer. And this paper reviews the development of TGF-β signaling pathway induced EMT in breast cancer.
Breast Neoplasms
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metabolism
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Epithelial Cells
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Epithelial-Mesenchymal Transition
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Humans
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Signal Transduction
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Transcription Factors
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Transforming Growth Factor beta
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physiology
8.Organic anion transporter system mediates the transport of aristolochic acid in tubular epithelial cells.
Yan-Yan WANG ; Yi-Pu CHEN ; Hong-Liang RUI
Acta Academiae Medicinae Sinicae 2009;31(4):476-480
OBJECTIVETo investigate whether aristolochic acid can be transported into human kidney proximal tubular cell (HKC) and its potential mechanism.
METHODSIntracellular aristolochic acid was measured by liquid chromatography-tandem mass spectrometry. The release of lactate dehydrogenase (LDH) induced by aristolochic acid in the presence of organic anion transporter inhibitor (probenecid) or organic cation transporter inhibitor (tetraethylammonium) was evaluated. The effects of probenecid on aristolochic acid induced connective tissue growth factor (CTGF) mRNA and protein expression were also examined by real time polymerase chain reaction and Western blot, respectively.
RESULTSAristolochic acid was detected in the suspension of the denatured HKC after incubation with aristolochic acid sodium salt. The release of LDH from HKC, which was induced by 60 mg/L aristolochic acid sodium salt, was significantly inhibited by 1 mmol/L probenecid (P < 0.01), but not by 1 mmol/L tetraethylammonium. The increased CTGF mRNA and protein expression in HKC stimulated by 40 mg/L aristolochic acid sodium salt was significantly down-regulated by 1 mmol/L probenecid (P < 0.05), with an inhibition rate of 16% and 21%, respectively.
CONCLUSIONAristolochic acid can be transported into HKC by organic anion transport system, and then exerts its biological effects.
Aristolochic Acids ; metabolism ; Connective Tissue Growth Factor ; metabolism ; Epithelial Cells ; metabolism ; Humans ; Kidney ; physiology ; Organic Anion Transporters ; metabolism
9.Ultrastructural and immunohistochemical studies on Trichomonas vaginalis adhering to and phagocytizing genitourinary epithelial cells.
Wen-lie CHEN ; Jin-fu CHEN ; Xiu-rong ZHONG ; Ping LIANG ; Wei LIN
Chinese Medical Journal 2004;117(3):376-381
BACKGROUNDTrichomonas vaginalis (T. vaginalis) belongs to a common sexually transmitted disease pathogen causing genitourinary trichomoniasis in both sexes. We investigated the pathogenetic mechanism of genitourinary trichomoniasis.
METHODSCultured T. vaginalis bodies were injected into the vaginas of rats, or incubated with genitourinary epithelial cells of female subjects, male subjects, and sperm. The ultrastructural and microscopic changes were observed via transmission and scanning electron microscopy and through microscopic histochemistry.
RESULTSGroups of T. vaginalis adhered to PAS positive columnar cells at the surface of stratified epithelium in the middle and upper portions of the vaginas. They also traversed under these cells. The parasites were shown to be PAS, cathepsin D, and actin positive, and they could release hydrolase into the cytoplasm of adhered epithelial cells. In the amebiform T. vaginalis, microfilaments were arranged into reticular formation. Similar phenomena were found during the interaction of T. vaginalis with host cells, both in vitro and in vivo. Usually several protozoa adhered to an epithelial cell and formed polymorphic pseudopodia or surface invaginations to surround and phagocytize the microvilli or other parts of the epithelial cytoplasm. Adhesion and phagocytosis of sperm by the protozoa occurred at 15 - 30 minutes of incubation. Digestion of sperm was found at 45 - 75 minutes and was complete at 90 - 105 minutes.
CONCLUSIONST. vaginalis tends to parasitize at the fornix of the vagina, because this is the site where columnar cells are rich in mucinogen granules and their microvilli are helpful for adhesion and nibbling. T. vaginalis possesses some invading and attacking abilities. Shape change, canalization, encystation, phagocytosis, digestion, the cell coat, cytoskeleton, and lysosome all play important roles in the process of adhesion. They have two methods of phagocytosis: nibbling and ingestion. Genitourinary epithelium may be injured directly by the digestive action of hydrolases, phagocytosis, and the mechanical action of pseudopodia.
Animals ; Cell Adhesion ; physiology ; Cells, Cultured ; Epithelial Cells ; physiology ; Humans ; Hydrolases ; metabolism ; Immunohistochemistry ; Male ; Phagocytosis ; physiology ; Rats ; Rats, Sprague-Dawley ; Trichomonas vaginalis ; metabolism ; ultrastructure ; Urogenital System ; cytology
10.Effect of Homeobox A13 transfection on epithelial-mesenchymal transition and bone morphogenetic protein-7 expression in kidney tubular epithelial cells.
Li PENG ; Qing-Nan HE ; Xiao-Yan LI ; Lan-Jun SHUAI ; Hai-Xia CHEN ; Yong-Zhen LI ; Zhu-Wen YI
Chinese Journal of Contemporary Pediatrics 2015;17(12):1342-1347
OBJECTIVETo examine the transfection of Homeobox A13 (HOXA13) on epithelial-mesenchymal transition (EMT) and the expression of bone morphogenetic protein-7 (BMP-7) induced by albumin-overload in human kidney tubular epithelial cells (HKCs).
METHODSThe cultured HKCs were treated with 20 mg/mL human serum albumin (HSA) for 48 hours. Protein expression of cytokeratin (CK), vimentin and HOXA13 in the HKCs was assessed by Western blot. Protein expression of CK, vimentin, and BMP-7 was also detected in HKCs transfected with lipofectamine contained HOXA13 DNA.
RESULTSHSA induced EMT in HKCs, presented by decreased CK expression (P<0.01) and increased vimentin expression (P<0.01). The up-regulated expression of HOXA13 transfected by lipofectamine inhibited the level of EMT induced by HSA in HKCs (P<0.05). The decreased rate of BMP-7 protein expression induced by HSA was inhibited by over-expressed HOXA13 in HKCs (P<0.05).
CONCLUSIONSTransfection of HOXA13 in HKCs could inhibit the degree of EMT induced by albumin-overload, possibly by increasing BMP-7 expression.
Bone Morphogenetic Protein 7 ; genetics ; Cells, Cultured ; Epithelial Cells ; metabolism ; Epithelial-Mesenchymal Transition ; Homeodomain Proteins ; physiology ; Humans ; Keratins ; genetics ; Kidney Tubules ; metabolism ; Transfection ; Vimentin ; genetics