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Biomedical subjects

R Wu

Publications and source records attributed to R Wu.

At least 73 records · Page 4Linked to original sources

Control of oligodendrocyte differentiation by the Nkx2.2 homeodomain transcription factor.

Oligodendrocytes are derived from glial precursors that arise from the ventral neural tube early in development. In the developing chicken CNS, oligodendrocyte progenitors selectively express Nkx2.2 homeodomain transcription factor, raising the possibility that Nkx2.2 may directly regulate oligogliogenesis. In this study, we have examined Nkx2.2 expression in rodent glial precursors and studied the effect of a loss of Nkx2.2 on oligodendrocyte and astrocyte differentiation. We show that Nkx2.2 is also expressed in mammalian oligodendrocyte progenitors and that the differentiation of MBP-positive and PLP-DM20-positive oligodendrocytes is dramatically retarded in Nkx2.2-null mutants along the entire rostrocaudal axis. In contrast, no effect is seen on astrocytic differentiation. Interestingly, absence of Nkx2.2 expression leads to a ventral expansion of the Olig1/Olig2 expression in neuroepithelial cells into the Nkx2.2 domain and a consequent increase in the production of Olig1/Olig2-positive and platelet-derived growth factor receptor alpha-positive oligodendrocyte progenitors. These results strongly suggest that Nkx2.2 regulates the differentiation and/or maturation, but not the initial specification, of oligodendrocyte progenitors. Consistent with this suggestion, overproduction of Nkx2.2 protein in fibroblast cells can induce gene expression from the proteolipid protein promoter.

3T3 Cells↗

[Research on fibrotic effect of Ni-Ti and 317L alloys in esophagus].

This study was conducted to examiune the fibrotic effect of Ni-Ti and 317L alloys in esophagus. The extract fluid from Ni-Ti, 317L alloys was made according to the ASTM standards of U.S.A. The Fb of esophageal scar was cultured primarily, then incubated with alloy abstract fluid. The proliferating activity of Fb was measured by MTT at 4, 24, 48, 72 hours in the course of culturing. The esophagus embedding test of Ni-Ti, 317L alloys was made according to ASTM standards of U.S.A. The tissue around the alloys was taken at weeks 2 and 12, and the pathologic changes were analysed. The results showed that Ni-Ti, 317L extract could depress the proliferating function of Fb gently, and the depressing action increased gradually with the culturing time. The result of embedding test was in accord with the ASTM standards of U.S.A. completely; the fibrotic membrane around the NiTi, 317L alloys became thinner with embedding time. These findings suggested that the scattering composition of Ni-Ti, 317L in body fluid might not activate the proliferating and secreting function of Fb, and the two alloys could not lead to fibrosis of esophagus aroun them.

Alloys↗

Preliminary interspecific genetic maps of the populus genome constructed from RAPD markers.

We have constructed RAPD-based linkage maps for an interspecific cross between two species of the genus Populus (P. adenopoda and P. alba), based on a double pseudo-test-cross strategy. Of a total of 360 polymorphic fragments scored, 290 showed a test-cross configuration, corresponding to DNA polymorphisms heterozygous in one parent and null in the other. In the female parent, P. adenopoda, 82 markers were grouped in 19 different linkage groups (553 cM), whereas in the male parent P. alba, 197 markers established a much more complete framework map with an observed genome length of 2300 cM covering 87% of the total P. alba genome. The larger number of test-cross markers detected for the P. alba parent than for the P. adenopoda parent might be due to a higher level of heterozygosity in the former than in the latter. In this study, we detected only a small percentage (2%) of the intercross dominant markers heterozygous in both parents and segregating 3:1 in the progeny. The further focus in this mapping study should be on the identification of more intercross markers, to align the two parent-specific maps into a consensus map for mapping important genes causing species differentiation during long evolutionary divergences.

Chromosome Mapping↗

Cytokine levels in various intravenous immunoglobulin (IVIg) preparations.

The mechanisms of action of intravenous immunoglobulin (IVIg) in autoimmune diseases include modulation of cytokine levels. We examined therefore whether direct infusion of abnormally high levels of 13 different cytokines or cytokine-inhibitors within 5 different IVIg preparations have any role in modulation of their levels. None of the measured cytokines in any of the IVIg preparations tested were above the normal levels, and regarding some no traces could be detected. Hence, modulation of cytokine levels following IVIg therapy involves other mechanisms such as interference with their secretion or cytokine-specific blocking antibodies, rather than direct infusion of cytokines.

Cytokines↗

[The role of beta-catenin in the repair of the damaged airway epithelium in smoking mice].

OBJECTIVE: To evaluate the role of beta-catenin(beta-cat) in the repair of the damaged airway epithelium by comparing their expressions of beta-cat in different stages of smoking in murine model. METHODS: With HE staining, morphological changes of airway epithelium were observed microscopically in mice model at 5th week (S5 w), 10th week (S10 w) and 15th week (S15 w) of smoking. Immunohistochemistry and hybridization in situ were performed to investigate the expressions of beta-cat mRNA, beta-cat, c-Src gene and phospho-rytyrosine-protein (p-Tyr). RESULTS: Morphological changes of the airway epithelium showed predominant damage(S5 w), repair(S10 w) and excessive proliferation (S15 w) Mean beta-cat OD values at S5 w, S10 w and S15 w were 0.097 +/- 0.007, 0.160 +/- 0.003 and 0.107 +/- 0.008, being significantly lower than the control value(0.204 +/- 0.012, all P < 0.01); The mean beta-cat mRNA OD value of S5 w, S10 w and S15 w were (0.123 +/- 0.011, 0.173 +/- 0.008 and 0.116 +/- 0.004) were also lower than that in control(0.223 +/- 0.008, all P < 0.01), but the OD value of S10 w was higher than those of S5 w and S15 w. OD value of S15 w was the lowest with only traced beta-cat mRNA expression in the nuclei. The expressions of c-Src and p-Tyr in normal airway epithelium(OD values: 0.048 +/- 0.015, 0.075 +/- 0.011) were significantly lower than those in S5 w(0.127 +/- 0.018, 0.112 +/- 0.012), S10 w (0.147 +/- 0.010, 0.127 +/- 0.018) and S15 w(0.147 +/- 0.010, 0.127 +/- 0.018, all P < 0.001). CONCLUSION: beta-cat may play an important role in the process of repair of airway epithelium. Downregulation of beta-cat may be caused by c-Src which phosphorylates tyrosin residues of beta-cat, leading to its degradation; Intracellular level of p-Tyr may, to some extent, reflect the functional condition of beta-cat.

Animals↗

[The research of pancadherin and beta-catenin expression in pulmonary tissue of mice with bleomycin-induced pulmonary fibrosis].

OBJECTIVE: To investigate the changes of pancadherin(Pan-cd) and beta-catenin(beta-cat) expression in pulmonary tissue of mice with bleomycin (BLM)-induced pulmonary injury and explore the relation between the Pan-cd/beta-cat expression and pulmonary fibrosis. METHOD: A single dose of BLM was intratracheally injected to induce pulmonary fibrosis of mice. Animals were killed and immunohistochemical methods were used with polyclonal anti-Pan-cd and anti-beta-cat antiserum. RESULTS: The expression of Pan-cd in type I alveolar cells was down-regulation. The expression of Pan-cd in type II alveolar cells was induced. The expression of Pan-cd and beta-cat in small airway epithelial cells were all down-regulation and were repeated with the way of down-regulation-reparation-down-regulation. The expression of Pan-cd on membrane in small airway epithelial cells decreased, whereas the cytoplasmic expression increased and was repeatedly alternated between cytoplasma with membrane. The expression of Pan-cd in alveolar macrophage and interstitial cells increased. CONCLUSION: The abnormal expression of cadherin and beta-cat may play a role in the pathogenesis of pulmonary fibrosis after pulmonary injury.

Animals↗

[Effects of mifepristone on expression of estrogen receptor and progesterone receptor in cultured human eutopic and ectopic endometria].

OBJECTIVE: To investigate the effects of mifepristone on expression of estrogen receptor (ER) and progesterone receptor (PR) in cultured human eutopic and ectopic endometria. METHODS: Endometrial (n = 22) and endometriotic (n = 12) tissues, obtained from patients with endometriosis, were cultured with and without mifepristone (1 x 10(-6) mol/L, 1 x 10(-4) mol/L) for 7-10 days. The expressions of ER, PR were determined by semi-quantitative immunocytochemistry method. Thirteen normal endometrial samples served as controls. RESULTS: The expressions of ER and PR in normal and eutopic endometrial cells showed the same cyclic pattern. The only difference was the significantly higher PR glandular content in eutopic endometria of endometriosis patients, as compared with normal controls [histochemistry score (H-score) 2.77 +/- 0.32 Vs 2.20 +/- 0.26 P < 0.05]. On the contrary, the ER, PR expressions in ectopic endometrial cells were significantly lower only during the proliferative phase (ER: gland 0.65-2.17 Vs 1.50-3.23, stroma 0.45-1.03 Vs 0.80-1.96; PR: gland 0.55-1.77 Vs 1.55-3.34, stroma 0.40-1.27 Vs 0.98-2.50; P < 0.05-0.01); significantly higher only during the late secretory phase (ER: gland 3.27 +/- 0.31 Vs 0.28 +/- 0.11, stroma 1.87 +/- 0.31 Vs 0.26 +/- 0.15; PR: gland 3.33 +/- 0.23 Vs 0.36 +/- 0.23) as compared with those of eutopic endometria. 10(-6)-10(-4) mol/L of mifepristone significantly suppressed the expressions of ER, PR in both eutopic and ectopic endometrial cells of endometriosis patients (P < 0.01) in a dose-dependent manner. CONCLUSIONS: Expression of ER, PR of endometriotic cells differed significantly from that of endometrial cells of patients with or without endometriosis. The down-regulatory effect on ER and PR may be one of the therapeutic mechanism of mifepristone on endometriosis.

Adult↗

Low power density microwave radiation induced early changes in rabbit lens epithelial cells.

OBJECTIVE: To determine whether low power density microwave radiation can induce irreversible changes in rabbit lens epithelial cells (LECs) and the mechanisms of the changes. METHODS: One eye of each rabbit was exposed to 5 mW/cm2 or 10 mW/cm2 power density microwaves for 3 hours, while the contralateral eye served as a control. Annexin V-propidium iodide (PI) two-color flow cytometry (FCM) was used to detect the early changes in rabbit lens epithelial cells after radiation. RESULTS: Lots of rabbit LECs were in the initial phase of apoptosis in the 5 mW/cm2 microwave radiation group. A large number of cells became secondary necrotic cells, and severe damage could be found in the group exposed to 10 mW/cm2 microwave radiation. CONCLUSION: Low power densities of microwave radiation (5 mW/cm2 and 10 mW/cm2) can induce irreversible damage to rabbit LECs. This may be the non-thermal effect of microwave radiation.

Animals↗

[Ultrastructural change of rabbit lens epithelial cells induced by low power level microwave radiation].

OBJECTIVE: To study the ultrastructural change of rabbit lens epithelial cells with transmission electron microscope and to observe whether low power level microwave can induce the injury of rabbit lens. METHODS: Eight rabbit eyes were exposed to 10 mW/cm(2) low power level microwave radiation for 30 hours. Transmission electron microscope was used to observe the ultrastructural changes of the lens epithelial cells. The other eye was served as self-control. RESULTS: The ultrastructure of exposed lens epithelial cells changed apparently. The characteristic apoptosis cell morphological changes, such as small cell size, the decreased number of mitochondria, balloon-shaped mitochondria, etc can be seen. No obvious changes can be found in the protected self-control eyes. CONCLUSIONS: The low power level microwave (10 mW/cm(2)) can induce the ultrastructural changes of rabbit lens epithelial cells, this may be the appearance of early irreversible microwave radiation injury. In regard to the pathogenic mechanism, it is necessary to perform further investigations.

Animals↗

[The enhanced mechanism of Cl- to SERS in silver colloid].

The SERS is enhanced when KCl is added to silver colloid and cation molecule. The hypothesis supposed that Cl- bridged between nano-silver and molecule, as a result the molecule adsorbing on nano-silver surface is promoted and the SERS is therefore enhanced. The CN- and NH3 can be better adsorbed when they are added separately to the nano-silver particles, Cl- and anion molecule. The SERS reduces when CN- and NH3 are added separately to Cl-, anion molecule and silver colloid. The result is that the CN- and NH3 are so strong that they have replaced Cl- and anion molecules. Therefore the SERS reduces. This has proved the bridge role of Cl-.

Adsorption↗

[Study on intramolecular energy transfer and relaxation processes of rare earth complexes by photoacoustic and fluorescence spectroscopy].

The excitation-relaxation processes of the solid Tb(III) complexes (Tb(AA)3.2H2O, Tb(AA)3 bpy and Tb(AA)3 phen) have been studied by photoacoustic spectroscopy (PAS) with the conjunction of fluorescence spectroscopy. The relaxation processes are studied from two aspects: nonradiative process and radiative process. The photoacoustic amplitude spectra and luminescence spectra of the complexes have been measured. Combined with the luminescence spectra, the PA amplitude spectra reflect the variation of the luminescence efficiency. According to the variation of the luminescence efficiency, the intramolecular energy transfer and relaxation processes of the complexes were studied. The suitability of the energy gap between the lowest triplet level of ligand and resonance energy level of rare earth ion is critical for efficient energy transfer.

Acoustics↗

[Regulatory effects of mifepristone and progesterone on the secretion of interleukin-6 by cultured eutopic and etopic endometrial cells].

OBJECTIVE: To investigate the regulatory effects of mifepristone and progesterone on the secretion of interleukin-6 (IL-6) by endometrial and endometriosis cells in vitro. METHODS: Primary cultures of eutopic and ectopic endometrial cells from 9 cases of endometriosis were exposed to mifepristone (10(-6) mol/L, 10(-4) mol/L) and progesterone (1 x 10(-7) mol/L, 1 x 10(-5) mol/L) respectively. IL-6 secretion was analyzed in the culture medium by enzyme linked immunosorbent assay (ELSA). RESULTS: Mifepristone inhibited the IL-6 secretion of ectopic endometrial cells, with the concentrations of IL-6 was (1 914.33 +/- 799.28) microg/L in the 1 x 10(-6) mol/L group (P < 0.01) and (990.25 +/- 58.40) microg/L in the 10(-4) mol/L group (P < 0.01). Progesterone also inhibited IL-6 secretion of ectopic endometrial cells, with (2 575.89 +/- 119.75) microg/L in the 1 x 10(-7) mol/L group (P < 0.05) and (1 736.25 +/- 750.89) microg/L in the 10(-5) mol/L group (P < 0.01). Mifepristone restrained the secretion of IL-6 by eutopic endometrial cells, with (346.96 < or = 24.32) microg/L in the 1 x 10(-6) mol/L group (P < 0.01) and (270.22 +/- 36.15) microg/L in the 1 x 10(-4) mol/L group (P < 0.01). All the effects of down regulation were more obvious when the concentrations of mifepristone and progesterone increased (P < 0.05 - 0.01) . Secretion of IL-6 by eutopic endometrial cells did not change significantly when incubated with progesterone (P > 0.05). CONCLUSION: The inhibitory effects on the secretion of IL-6 by ectopic and (or) eutopic endometrium may provide one of the cellular therapeutic mechanisms of mifepristone and progesterone on endometriosis.

Cells, Cultured↗

[Expression of T-lymphocytes and cytokines in the decidua of mifepristone with misoprostol for terminating early pregnancy].

OBJECTIVE: To investigate the expression of T-lymphocyte subsets (CD3+, CD4+, CD8+), natural killer cells (NK cells, CD56+, CD16+), tumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta (TGF-beta) in mifepristone and misoprostod treated ducidua for terminating human early pregnancy. METHODS: Thirty eight women who volunteered to terminate their pregnancy were divided into 3 groups: mifepristone group (group I, n = 13), mifepristone with misoprostol group (group II, n = 12) and control group (group Il, n = 13), The expression of T-lymphocyte subsets, NK cells, TNF-alpha and TGF-beta were assessed by flow cytometry. RESULTS: The expression of CD4+ were (30.91 +/- 2.57)% and (31.58 +/- 3.28)% in group I and II respectively. Which were significantly higher than that in group III (25.64 +/- 2.36)% (P < 0.05, P < 0.01). CD56+ were (22.40 +/- 2.77)% and (26.88 +/- 3.79)% in group I and II, which were significantly higher than that in group III (18.58 +/- 4.04)% (P < 0.05, P < 0.01), CD16+ were (8.98 +/- 2.18)% and (10.84 +/- 2.51)% in group I and II, which were significantly higher than that in group III (6.34 +/- 2.01)% (P < 0.01, P < 0.001). The expression of TNF-alpha in group I and II were higher than that of group III, TGF-beta in group I and II were lower than that of group III, but there was no significant difference (P > 0.05). The expression of CD3+, CD8+, CD4+/ CD8+ ratio were not significant difference among the three groups (P > 0.05). CONCLUSIONS: Mifepristone with misoprostol for terminating early pnegnancy might be affect the expression of lymphocyte and cytokines and induce the disorder of decidual micro-environment which might be the reason of medical abortion.

Abortifacient Agents↗

[Mifepristone following conservative surgery in the treatment of endometriosis].

OBJECTIVE: To compare the efficacy and safety of mifepristone and danazol after conservative surgery in the treatment of patients with endometriosis. METHODS: Sixty-one patients with endometriosis (RAFS stage I-IV ) after conservative surgery were treated orally either with mifepristone 10 mg/d (group M, n = 31) or danazol 200 mg 2-3 times/d (group D, n = 30) for 3 months. Changes of symptoms and signs, serum reproductive hormone levels as well as side effects were assessed before and at the end of therapy. Moreover, biochemical parameters of bone metabolism: urinary deoxypyridine /creatinine (UDpd/Cr), serum alkaline phosphatase (AKP) and bone gala-protein (BGP) were also measured before and after treatments. RESULTS: During treatment symptoms and signs were remarkbly relieved in both groups. Side effects including hot flushes, irregular vaginal bleeding, back pain, weight gain and acne, were less commnly seen in group M as compared with group D. Serum luteal hormone (LH), follicular stimulating homone (FSH) levels remained in the range of follicular phase in both groups. So was serum estradiol (E2) levels in group M[(204.9 +/- 45.3 ) pmol/L], but declined to postmenopausal level in group D [(94.3 +/- 33.0) pmol/L]. About two weeks after discontinuation of the thrapy, serum E2 levels [(1,221.6 +/- 384.2) pmol/L] was not significantly different from the normal ovulatory range in group M, but significantly lower in group D [(815.1 +/- 376.0) pmo/L, P < 0.05] . So were the serum progesterone levels at mid-luteal phase [(33.1 +/- 5.6) nmol/L Vs (27.4 +/- 4.9) nmol/L]. There were no significant changes of biochemical parameters of bone metabolism before and at the end of treatment except significant increases of serum AKP and BGP in group D. CONCLUSIONS: Mifepristone is equally effective to danazol when combined with conservative surgery in the management of endometriosis with fewer side effects. Serum E2 levels remained in the range of follicular phase. No impact on the bone turnover after 3 months of therapy was found.

Bone Remodeling↗

Role of the calcium-independent transient outward current I(to1) in shaping action potential morphology and duration.

The Kv4.3-encoded current (I:(Kv4.3)) has been identified as the major component of the voltage-dependent Ca(2+)-independent transient outward current (I:(to1)) in human and canine ventricular cells. Experimental evidence supports a correlation between I:(to1) density and prominence of the phase 1 notch; however, the role of I:(to1) in modulating action potential duration (APD) remains unclear. To help resolve this role, Markov state models of the human and canine Kv4.3- and Kv1.4-encoded currents at 35 degrees C are developed on the basis of experimental measurements. A model of canine I:(to1) is formulated as the combination of these Kv4.3 and Kv1.4 currents and is incorporated into an existing canine ventricular myocyte model. Simulations demonstrate strong coupling between L-type Ca(2+) current and I:(Kv4.3) and predict a bimodal relationship between I:(Kv4.3) density and APD whereby perturbations in I:(Kv4.3) density may produce either prolongation or shortening of APD, depending on baseline I:(to1) current level.

Action Potentials↗

Somatic mutations of fibroblast growth factor receptor 3 (FGFR3) are uncommon in carcinomas of the uterine cervix.

Germline mutations of the gene encoding human fibroblast growth factor receptor 3 (FGFR3) have been shown to be responsible for several related autosomal dominant forms of syndromic craniosynostosis and short limb dwarfism. Somatic activating mutations of FGFR3 were recently reported to occur in three of 12 (25%) uterine cervical carcinomas and nine of 26 (35%) bladder carcinomas, suggesting that constitutive activation of FGFR3 may be an important mechanism underlying the development and/or progression of these common epithelial malignancies. In order to investigate further a possible role for FGFR3 mutations in cervical carcinogenesis, we performed sequence-based mutational analysis of FGFR3 in 51 primary cervical carcinomas and seven cervical carcinoma-derived cell lines. The regions analysed (exons 7, 10, 13, 15, and 19) encompassed all previously described FGFR3 mutations. A single nucleotide substitution at codon 249, predicting a serine to cysteine amino acid substitution (S249C) in the FGFR3 extracellular domain, was identified in one primary tumor. Only wild type FGFR3 alleles were identified in the remaining tumors and cell lines. The S249C mutation is the only FGFR3 mutation described to date in cervical carcinomas. These findings suggest that while activating mutations of FGFR3 occur in cervical cancer, they may not be as common as initially reported.

Blotting, Northern↗