共查询到20条相似文献,搜索用时 31 毫秒
1.
Rat pleural mesothelial cells in culture 总被引:5,自引:0,他引:5
M. C. Jaurand J. F. Bernaudin A. Renier H. Kaplan J. Bignon 《In vitro cellular & developmental biology. Plant》1981,17(2):98-106
Summary A culture system has been developed for long-term maintenance of rat pleural mesothelial cells. Mesothelial cells were isolated
from the parietal pleura of rats and cultured in NCTC 109 medium supplemented with 10% fetal bovine serum. The cell explants
attached to the dish and formed a confluent monolayer of polygonal cells within 10 to 15 days. Subcultures were made in the
same medium. The mean population doubling time was approximately 30 hr. The ultrastructure of the mesothelial cells in culture
was studied by light and electron microscopy and was compared with that of cells obtained from submesothelial components.
This work was supported by CEE Grant No. 264 77 6 ENV F. 相似文献
2.
Yasuhiro Kuramitsu Hiromu Miyamoto Toshiyuki Tanaka Xiulian Zhang Masanori Fujimoto Kazuhiro Ueda Toshiki Tanaka Kimikazu Hamano Kazuyuki Nakamura 《Proteomics》2009,9(22):5078-5089
We performed proteomic differential display analysis of human malignant pleural mesothelioma (MPM) cell lines and a human pleural mesothelial cell line by using 2‐DE and LC‐MS/MS. The human MPM cell lines were NCI‐H28, NCI‐H2052 and NCI‐H2452, and the human pleural mesothelial cell line was MeT‐5A. Between MeT‐5A and NCI‐H2052, we found 38 protein spots whose expression levels were different, from the results of 2‐DE; 28 protein spots appeared higher, and 10 other protein spots lower in NCI‐H2052 than in MeT‐5A. These spots were analyzed by LC‐MS/MS analysis and identified by a peptide sequence tag. However, from the results of 2‐DE of the other cell lines, there was only one consistently upregulated protein, astrocytic phosphoprotein PEA‐15, in all three MPM cell lines. Western blotting using specific antibodies against PEA‐15 confirmed the elevated expression level of PEA‐15 in all three MPM cell lines compared with MeT‐5A cells and normal pleura tissues from patients. PEA‐15 was knocked down in NCI‐H2052 cells, and the proliferation of PEA‐15‐silenced NCI‐H2052 cells was suppressed 7–15% compared with negative control cells. These results suggest that PEA‐15 expression is likely to be associated with the tumorigenesis of MPM. 相似文献
3.
John F. Aronson 《In vitro cellular & developmental biology. Plant》1983,19(8):642-650
Summary Human retinal pigment epithelium (RPE)-derived cell lines were established from RPE-covered choroid tissue fragments, which
had been generated by culture on nontissue culture plastic. Two phenotypes were apparent in a given line: (a) a compact cell
which formed domes and ultimately melanosomes before being sloughed; and (b) a squamous cell which was often elongated and
which bound antibody to human keratins. This latter cell did not become black or form domes. The average number of cell doublings
for the 13 lines tested was between 15 and 40 when cultured in a modified Eagle's minimum essential medium containing 10%
fetal bovine serum. Cell lines newly established from material that had been in culture for more than 6 months had normal
mitotic chromosomes and still developed areas with strongly pigmented cells when refed. Normal human epithelial cell lines
of this kind may be useful in studies of cell aging and defining change associated with the development of neural cells from
ectoderm.
This work was supported by U.S. Public Health Service Grant AG-00378 to Dr. V. J. Cristofalo. 相似文献
4.
Apollo Pronk Piet Leguit Arthur A. G. M. Hoynck van Papendrecht Edwin Hagelen Theo J. M. V. van Vroonhoven Henri A. Verbrugh 《In vitro cellular & developmental biology. Animal》1993,29(2):127-134
Summary Normal human mesothelial cells (NHMC) were isolated from pieces of human omentum. The cell yield was approximately one million
cells per square centimeter omentum. The mesothelial cells were identified by their positive staining with monoclonal antibodies
against cytokeratins 6 and 18. Transmission electronmicroscopy of cultured NHMC revealed many microvilli on the apical surface
and many mitochondria and pinocytotic vesicles in the cytoplasm, indicating active transmembrane transport. Growth of NHMC
was directly related to the concentration of human serum or of fetal bovine serum in the growth medium. Addition of epidermal
growth factor with or without hydrocortisone resulted in a significant increase of NHMC growth; when endothelial cell growth
factor, insulin, or hydrocortisone were added no such increase was observed. Seeding NHMC at densities less than 3000/cm2 did not result in monolayer formation. The mesothelial cells were serially passed in growth medium M199 with added 10% fetal
bovine serum up to 7 passages. However, after Passage 4 the cells changed into giant cells with an irregular pattern, and
a lack of intracellular cytokeratin expression was observed for most of the cells. 相似文献
5.
Melican D Butler R Hawkins N Chen LH Hayden E Destrempes M Williams J Lewis T Behboodi E Ziomek C Meade H Echelard Y Gavin W 《Theriogenology》2005,63(6):1549-1563
This work was performed within a commercial nuclear transfer program to investigate different methods for synchronizing donor cell cycle stage, for harvesting donor cells, and for fusion and activation of reconstructed caprine embryos. Primary fetal cells isolated from day 35 to day 40 fetuses were co-transfected with DNA fragments encoding both the heavy and light immunoglobulin chains of three different monoclonal antibodies and neomycin resistance. Four neomycin resistant cell lines for each antibody were selected, expanded, and aliquots were both cryopreserved for later use as karyoplast donors or used for further genetic characterization. Transfected fetal cells were cultured in 0.5% FBS to synchronize G0/G1 cell cycle stage cells, then re-fed with 10% FBS prior to use to allow donor cells to re-enter the cell cycle. Alternatively, transfected fetal cells were grown to confluence in 10% FBS to induce contact inhibition to synchronize G0/G1 cell cycle stage cells. Adherent monolayers of transfected fetal donor cells were harvested by either partial or complete trypsinization. Donor cells were simultaneously fused and activated with enulceated in vivo produced ovulated oocytes from superovulated does. Half of the fused couplets received an additional electrical activation pulse and non-fused couplets were re-fused. Four live offspring were produced from 587 embryos generated from cell lines cultured in 0.5% FBS, while one live offspring was produced from 315 embryos generated from cell lines cultured in 10% FBS (0.7% versus 0.3% embryos transferred, respectively, P > 0.05). Five offspring were produced from 633 embryos generated from cell lines harvested by partial trypsinization (0.8% embryos transferred), and no offspring were produced from 269 embryos generated from cell lines harvested by complete trypsinization. Four live offspring were produced from 447 embryos generated from re-fused couplets, and one live offspring was produced from 230 embryos generated from fused couplets that received an additional electrical activation pulse (0.9% versus 0.4% embryos transferred, respectively, P > 0.05). These results suggest that low-serum culture of transfected goat fetal cells and harvest by partial trypsinization may be more efficient methods for generating transgenic goats by somatic cell nuclear transfer. In addition, re-fusion of non-fused couplet or an additional activation step was successful for producing live offspring. 相似文献
6.
Failure of simian virus 40 small t antigen to disorganize actin cables in nonpermissive cell lines. 总被引:14,自引:10,他引:4
下载免费PDF全文
![点击此处可从《Journal of virology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Mouse C3H 10T1/2 cell lines expressing the simian virus 40 (SV40) small t antigen were obtained by cotransfection of pSV2neo and plasmids which encode small t. Cell lines derived from two plasmids which encode small t in the absence of stable deletion fragments of the large T antigen were morphologically normal and grew to slightly higher saturation densities in low serum than control cell lines. Unexpectedly, the clones had highly organized actin cables, as did parental 10T1/2 cells infected with wild-type SV40. These observations and comparisons of rat F111 cells infected with either polyomavirus or SV40 suggest that the SV40 small t antigen does not directly affect cytoskeletal organization. 相似文献
7.
A. L. Sherwood S. E. Mutsaers V. K. Peeva C. Robinson C. J. DeSilva N. R. Swanson R. A. Lake 《Cell proliferation》2008,41(6):894-908
Abstract. Objectives: Mesotheliomas occur in occult serous cavities after chronic exposure of mesothelial cells to asbestos fibres. Molecular events that contribute to the development of this cancer are therefore not readily accessible for study. We have used in vitro culture systems to study and compare induced and spontaneous transformation events in primary mouse mesothelial cells. Materials and methods: Mouse mesothelial cells were cultivated until small populations of proliferating cells emerged from senescing cultures. Spontaneously transformed cultures of cells were characterized and compared to malignantly transformed cells. Results: Human mesothelial cells had a finite lifespan of 10–15 population doublings when cultured in vitro; mouse mesothelial cells typically exhibit this same pattern. Here, we show that mouse mesothelial cells can be cultured for extended periods and that these cells can transform spontaneously. Lines of spontaneously transformed cells generated in this study are immortal and growth factor‐independent. They display the salient characteristic features of transformation, including increased proliferation rate, lack of contact inhibition, aneuploidy and ability to grow in anchorage‐independent conditions. A subset of these cell lines developed into tumours in syngeneic mice. Comparative gene expression analysis demonstrated that spontaneously transformed cell lines were more closely related to neoplastic cells than to primary cells. Conclusion: These findings have implications for interpretation of in vitro transformation studies, demonstrating broad similarity between spontaneous and induced genetic changes. 相似文献
8.
HGF/SF Induces Mesothelial Cell Migration and Proliferation by Autocrine and Paracrine Pathways 总被引:7,自引:0,他引:7
Richard Warn Pascale Harvey Alba Warn Adam Foley-Comer Paraskevi Heldin Marjan Versnel Naokatu Arakaki Yasushi Daikuhara Geoffrey J. Laurent Sarah E. Herrick Steven E. Mutsaers 《Experimental cell research》2001,267(2):258-266
Mesothelial repair differs from that of other epithelial-like surfaces as healing does not occur solely by centripetal in-growth of cells as a sheet from the wound margins. Mesothelial cells lose their cell-cell junctions, divide, and adopt a fibroblast-like morphology while scattering across and covering the wound surface. These features are consistent with a cellular response to hepatocyte growth factor/scatter factor (HGF/SF). In this study, we examined the ability of mesothelial cells to secrete HGF/SF and investigated its possible role as an autocrine regulator of mesothelial cell motility and proliferation. We found that human primary mesothelial cells expressed HGF/SF mRNA and secreted active HGF/SF into conditioned medium as determined by ELISA and in a scattering bioassay. These cells also expressed the HGF/SF receptor, Met, as shown by RT-PCR and by Western blot analysis and immunofluorescence. Incubation of mesothelial cells with neutralizing antibodies to HGF/SF decreased cell migration to 25% of controls, whereas addition of HGF/SF disrupted cell-cell junctions and induced scattering and enhanced mesothelial cell migration. Furthermore, HGF/SF showed a small but significant mitogenic effect on all mesothelial cell lines examined. In conclusion, HGF/SF is produced by mesothelial cells and induces both motility and proliferation of these cells. These data are consistent with HGF/SF playing an autocrine role in mesothelial healing. 相似文献
9.
Development of two cloned epithelial cell lines from normal adult mouse and rat ventral prostates 总被引:1,自引:0,他引:1
Yoshinobu Kubota Eugene B. Gehly Karl H. Link Charles Heidelberger 《In vitro cellular & developmental biology. Plant》1981,17(11):965-978
Summary Two epithelial cell lines were established, one from adult C3H mouse and one from adult Fischer rat ventral prostate. These
cell lines were obtained from explant cultures, using Ham's F12 medium supplemented with HEPES, insulin, testosterone, hydrocortisone,
epidermal growth factor, and 7.5% fetal bovine serum. A low concentration of trypsin and EDTA in Ca++-and Mg++-free phosphate buffer was used for passaging the cells. The rat cell line was established following implantation of prostate
tissue in nude mice. These cell lines stained positively for acid phosphatase and were dependent upon epidermal growth factor
for growth. Morphological studies, including electron microscopy, revealed a highly characteristic epithelial morphology of
both cell lines. These cell lines have hypotetraploid chromosome numbers and are capable of metabolizing benzo(a)pyrene. We propose the application of these cells as models for the study of prostate carcinogenesis.
This work was supported in part by Grant CA-21, 746, and by the Electron Microscope Core Facility on Grant CA-14,089, from
the National Cancer Institute, National Institutes of Health, Bethesda, MD. 相似文献
10.
Establishment of permanent cell lines purified from human mesothelioma: morphological aspects,new marker expression and karyotypic analysis 总被引:1,自引:1,他引:0
Philippeaux MM Pache JC Dahoun S Barnet M Robert JH Mauël J Spiliopoulos A 《Histochemistry and cell biology》2004,122(3):249-260
This study reports the establishment of three major subtypes of human mesothelioma cells in tissue culture, i.e. the epithelioid, sarcomatoid and biphasic forms, and compares their phenotypic and biological characteristics. Primary cells isolated from biopsies or pleural exudates were subcultured for over 50 passages. We evaluated immunoreactivity using various mesothelial markers related to histological patterns of these cell lines. For epithelioid cells, calretinin and cytokeratin were found to be useful and easily interpretable markers as for control mesothelial cells. The biphasic form was only partially positive and the sarcomatoid type negative. Vimentin was expressed by all cell lines. BerEP4, a specific marker for adenocarcinoma, was negative. Interestingly, while the macrophage marker CD14 was negative, immunoreactivity for a mature macrophage marker (CD68) was expressed by all cell types, suggesting that this marker might constitute an additional tool useful in the differential diagnosis of mesothelioma. At the ultrastructural level, a cell surface rich in microvilli confirmed their mesothelial origin. PCR analysis revealed that none of the cell lines contained SV40 DNA. Karyotypic analyses showed more complex abnormalities in the epithelioid subtype than in the sarcomatoid form. These cell lines may be useful in the study of cellular, molecular and genetic aspects of the disease. 相似文献
11.
Kanamori-Katayama M Kaiho A Ishizu Y Okamura-Oho Y Hino O Abe M Kishimoto T Sekihara H Nakamura Y Suzuki H Forrest AR Hayashizaki Y 《PloS one》2011,6(10):e25391
Background
Mesothelioma is a highly malignant tumor that is primarily caused by occupational or environmental exposure to asbestos fibers. Despite worldwide restrictions on asbestos usage, further cases are expected as diagnosis is typically 20–40 years after exposure. Once diagnosed there is a very poor prognosis with a median survival rate of 9 months. Considering this the development of early pre clinical diagnostic markers may help improve clinical outcomes.Methodology
Microarray expression arrays on mesothelium and other tissues dissected from mice were used to identify candidate mesothelial lineage markers. Candidates were further tested by qRTPCR and in-situ hybridization across a mouse tissue panel. Two candidate biomarkers with the potential for secretion, uroplakin 3B (UPK3B), and leucine rich repeat neuronal 4 (LRRN4) and one commercialized mesothelioma marker, mesothelin (MSLN) were then chosen for validation across a panel of normal human primary cells, 16 established mesothelioma cell lines, 10 lung cancer lines, and a further set of 8 unrelated cancer cell lines.Conclusions
Within the primary cell panel, LRRN4 was only detected in primary mesothelial cells, but MSLN and UPK3B were also detected in other cell types. MSLN was detected in bronchial epithelial cells and alveolar epithelial cells and UPK3B was detected in retinal pigment epithelial cells and urothelial cells. Testing the cell line panel, MSLN was detected in 15 of the 16 mesothelioma cells lines, whereas LRRN4 was only detected in 8 and UPK3B in 6. Interestingly MSLN levels appear to be upregulated in the mesothelioma lines compared to the primary mesothelial cells, while LRRN4 and UPK3B, are either lost or down-regulated. Despite the higher fraction of mesothelioma lines positive for MSLN, it was also detected at high levels in 2 lung cancer lines and 3 other unrelated cancer lines derived from papillotubular adenocarcinoma, signet ring carcinoma and transitional cell carcinoma. 相似文献12.
目的:定腹膜间皮细胞在高糖引起上皮间质转化(Epithelial—mesenchymnal transition,EMT)过程中microRNA的表达差异。方法:常规培养PMC细胞,利用高糖培养液刺激诱导腹膜间皮细胞发生EMT,倒置显微镜观察各组细胞形态学变化,实时定量PCR检测EMT标志基因变化,以此确定高糖诱导EMT的发生。利用特异茎环结构的引物合成microRNA的cDNA,实时定量PCR检测重要microRNA的表达变化。结果:高糖培养液培养腹膜间皮细胞48hr后,细胞形态呈梭形改变,同时EMT标记基因E—cadherin表达明显减低(P〈0.01),Vimentin表达显著升高(P〈0.01),说明高糖诱导腹膜间皮细胞发生了EMT。利用microRNA特异的茎环结构引物,实时定量PCR检测结果发现高糖刺激后miR-193a的表达明显上调(P〈0.01);miR-15a和let-7e的表达明显降低(P〈0.01);miR-16和miR-21的表达无明显变化(P〉0.05),同时检测发现高糖刺激后miR-193a的表达水平随刺激时间表达升高。结论:异常变化的microRNA可能对高糖诱导的腹膜间皮细胞EMT具有重要调控作用。 相似文献
13.
14.
Binding of ovarian cancer cells to immobilized hyaluronic acid 总被引:2,自引:0,他引:2
Jonathan B Catterall Michael J Gardner Lindsay M.H Jones Graham A Turner 《Glycoconjugate journal》1997,14(7):867-869
Ovarian cancer has the highest mortality rate of any gynaecological malignancy. This is caused by metastatic deposits obstructing
the intestinal tract. Very little is known about the molecules involved in the initial attachment of the metastatic tumour
cells to the peritoneal mesothelial lining. Previously, we showed that many ovarian tumour lines express the adhesion molecule,
CD44, on their cell surface. The major ligand for CD44 is the extracellular matrix glycosaminoglycan, hyaluronic acid (HA).
Because mesothelial cells have a pericellular cost that contains large amounts of HA, it was postulated that the CD44/HA interaction
is an important stage in ovarian cancer spread. However, it was difficult to demonstrate this interaction in an in vitro adhesion
assay with mesothelial cells as most of the HA, and presumably the bound tumour cells, were lost from the mesothelial cells
during the washing steps of the assay. In order to try and clarify the situation, the adhesion of six ovarian tumour lines
to immobilized HA was measured. Four lines expressed high levels of CD44 and two lines expressed negligible amounts. Preliminary
experiments were carried out with one of the CD44-expressing lines. After coating a plate overnight with 3 mg ml−1 HA, the
5 min adhesion of this line varied between 2% and 73% according to the type of plate that was used. Falcon Micro Test III
flexible plates gave the highest adhesion and was used for further experiments. Plates were coated with concentrations of
HA between 0.001 mg ml−1 and 3 mg ml−1. All CD44 expressing lines adhered to HA, but the maximum adhesion and the adhesion
strength varied with the line studied and was not closely related to the total CD44 expression. These results suggest that
CD44 on ovarian tumour cells binds to HA on mesothelial cells. As much of the HA can be very easily lost from the mesothelial
cell surface, additional factors such as the strength of the CD44/HA interaction, and the formation of bonds by the tumour
cells with other membrane adhesion molecules, such as integrins, are also important in promoting tumour spread.
This revised version was published online in November 2006 with corrections to the Cover Date. 相似文献
15.
Marc Schlaeppi Curzio Rü egg Chien Tr n-Thang Germain Chapuis Hendrik Tevaearai Harald Lahm Bernard Sordat 《Cell communication & adhesion》1997,4(6):439-455
Peritoneal carcinomatosis involves a series of events including tumor cell interactions with mesothelial cells and the extracellular matrix (ECM). We have studied the adhesive and invasive properties of four human colorectal carcinoma cell lines (Co115, HT29, SW480, SW620) confronted in vitro with a human mesothelial cell monolayer or with the ECM proteins collagen IV, laminin-1, fibronectin, tenascin-C and vitronectin. Quantitation was achieved following staining of tumor cells with the calcein-AM fluorescent dye. We found that all four cell lines rapidly adhered to a mesothelial cell monolayer. This adhesion event was not inhibitable by anti-integrin and anti-CD44 antibodies. Following initial attachment, the SW480 and SW620 cells invaded the mesothelial cell monolayer more aggressively than HT29 and Col 15 cells. All cell lines adhered to ECM proteins with each one exhibiting an individual adhesion pattern. Adhesion to matrix was completely integrin-dependent. When tested in an invasion assay, HT29 and Co115 cells crossed Matrigel-coated filters while SW480 and SW620 cells did not. This invasion was inhibited by anti-β1 integrin antibodies. Taken together, our results demonstrate that the initial colorectal tumor cell—mesothelial cell interaction occurs through an integrin-independent mechanism while adhesion to matrix proteins and invasion through Matrigel are integrin-dependent events. Furthermore, the different invasive capacity of SW480 and SW620 versus HT29 and Co115 cells upon interaction with a mesothelial cell monolayer or Matrigel suggests that these two invasion events may be mediated by distinct mechanisms. 相似文献
16.
The mesothelium consists of a single layer of flattened mesothelial cells that lines serosal cavities and the majority of internal organs, playing important roles in maintaining normal serosal integrity and function. A mesothelial 'stem' cell has not been identified, but evidence from numerous studies suggests that a progenitor mesothelial cell exists. Although mesothelial cells are of a mesodermal origin, they express characteristics of both epithelial and mesenchymal phenotypes. In addition, following injury, new mesothelium regenerates via centripetal ingrowth of cells from the wound edge and from a free-floating population of cells present in the serosal fluid, the origin of which is currently unknown. Recent findings have shown that mesothelial cells can undergo an epithelial to mesenchymal transition, and transform into myofibroblasts and possibly smooth muscle cells, suggesting plasticity in nature. Further evidence for a mesothelial progenitor comes from tissue engineering applications where mesothelial cells seeded onto tubular constructs have been used to generate vascular replacements and grafts to bridge transected nerve fibres. These findings suggest that mesothelial cell progenitors are able to switch between different cell phenotypes depending on the local environment. However, only by performing detailed investigations involving selective cell isolation, clonal analysis together with cell labelling and tracking studies, will we begin to determine the true existence of a mesothelial stem cell. 相似文献
17.
Jonathan B Catterall Michael J Gardner Lindsay M.H Jones Graham A Turner 《Glycoconjugate journal》1997,14(5):647-649
Ovarian cancer has the highest mortality rate of any gynaecological malignancy. This is caused by metastatic deposits obstructing
the intestinal tract. Very little is known about the molecules involved in the initial attachment of the metastatic tumour
cells to the peritoneal mesothelial lining. Previously, we showed that many ovarian tumour lines express the adhesion molecule,
CD44, on their cell surface. The major ligand for CD44 is the extracellular matrix glycosaminoglycan, hyaluronic acid (HA).
Because mesothelial cells have a pericellular cost that contains large amounts of HA, it was postulated that the CD44/HA interaction
is an important stage in ovarian cancer spread. However, it was difficult to demonstrate this interaction in an in vitro adhesion
assay with mesothelial cells as most of the HA, and presumably the bound tumour cells, were lost from the mesothelial cells
during the washing steps of the assay. In order to try and clarify the situation, the adhesion of six ovarian tumour lines
to immobilized HA was measured. Four lines expressed high levels of CD44 and two lines expressed negligible amounts. Preliminary
experiments were carried out with one of the CD44-expressing lines. After coating a plate overnight with 3 mg ml-1 HA, the
5 min adhesion of this line varied between 2% and 73% according to the type of plate that was used. Falcon Micro Test III
flexible plates gave the highest adhesion and was used for further experiments. Plates were coated with concentrations of
HA between 0.001 mg ml−1 and 3 mg ml−1. All CD44 expressing lines adhered to HA, but the maximum adhesion and the adhesion
strength varied with the line studied and was not closely related to the total CD44 expression. These results suggest that
CD44 on ovarian tumour cells binds to HA on mesothelial cells. As much of the HA can be very easily lost from the mesothelial
cell surface, additional factors such as the strength of the CD44/HA interaction, and the formation of bonds by the tumour
cells with other membrane adhesion molecules, such as integrins, are also important in promoting tumour spread.
This revised version was published online in November 2006 with corrections to the Cover Date. 相似文献
18.
J Fleury-Feith M Nebut L Saint-Etienne P Laurent M C Pinchon L Kheuang A Renier M C Jaurand 《Biology of the cell / under the auspices of the European Cell Biology Organization》1989,65(1):45-50
Rat pleural mesothelial cells treated in vitro with chrysotile fibers have been successfully transplanted into nude mice. Three cultures (1 untreated, 2 treated) were injected at passage 75; a fourth culture was obtained from a mesothelioma induced in rat by chrysotile fibers. Overall, tumors grew in each series, but the delay between cell injection and tumor formation was 22 wk with untreated cells whereas only 1 or 2 wk were needed with treated cells, and 1 wk with cells from in vivo-induced mesothelioma. Pathological study by light and electron microscopy of tumors is reported here and showed the mesothelial nature of the cells. Comparison between the ultrastructure of the injected cells and tumor cells indicated that the morphology of injected cells was retained in tumors even if the delay in tumor formation was long. These results suggest that this model is useful for investigating mesothelial cell transformation resulting from in vitro or in vivo exposure to certain carcinogens. 相似文献
19.
Chronic inflammation is associated with inducible nitric oxide synthase expression in infiltrating and resident cells (epithelia, neurons) and an exaggerated release of nitric oxide. NO can induce apoptosis in macrophages and tumour cell lines. We investigated whether NO induced cell death in an epithelial (T84) cell fine via apoptosis. Culture T84 cells were exposed to a bolus of NO (40 or 80 muM) dissolved in Hank's balanced salt solution (HBSS) supplemented with 10% fetal calf serum (FCS). After incubation for 4 h at 37( degrees )C in 5% CO(2), cells were either stained for DNA fragmentation with the TdT-mediated dUTP-biotin nick end labelling (TUNEL) method, or cytosolic DNA fragments quantified by a cell death detection ELISA assay. Nitric oxide induced apoptosis in a dose-dependent manner which preceded frank cell death (failure to exclude Trypan blue). These data suggest that epithelial cell death may be NO dependent and via apoptosis, in states of gut inflammation. 相似文献
20.
Fromigué O Hamidouche Z Chateauvieux S Charbord P Marie PJ 《Journal of cellular biochemistry》2008,104(2):620-628
Bone marrow-derived mesenchymal stem cells (MSC) are able to differentiate into osteoblasts under appropriate induction. Although MSC-derived osteoblasts are part of the hematopoietic niche, the nature of the stromal component in fetal liver remains elusive. Here, we determined the in vitro osteoblastic differentiation potential of murine clonal fetal liver-derived cells (AFT024, BFC012, 2012) in comparison with bone marrow-derived cell lines (BMC9, BMC10). Bone morphogenetic protein-2 (BMP2) increased alkaline phosphatase (ALP) activity, an early osteoblastic marker, in AFT024 and 2012 cells, whereas dexamethasone had little or no effect. BMP2, but not dexamethasone, increased ALP activity in BMC9 cells, and both inducers increased ALP activity in BMC10 cells. BMP2 increased ALP mRNA in AFT024, 2012 and BMC9 cells. By contrast, ALP was not detected in BMC10 and BFC012 cells. BMP2 and dexamethasone increased osteopontin and osteocalcin mRNA expression in 2012 cells. Furthermore, bone marrow-derived cells showed extensive matrix mineralization, whereas fetal liver-derived cell lines showed no or very limited matrix mineralization capacity. These results indicate that the osteoblast differentiation potential differs in bone marrow and fetal liver-derived cell lines, which may be due to a distinct developmental program or different microenvironment in the two hematopoietic sites. 相似文献