ABSTRACT
BACKGROUND: The difference in diagnostic yield between surgical lung biopsy and transbronchial lung cryobiopsy (TBLC) in diffuse parenchymal lung diseases (DPLD) has been reported to be due to differences in the rate of interpathologist agreement, specimen size, and specimen adequacy. In TBLC, the specimens containing large airway components are generally believed as inadequate specimens for histological evaluation, but the detailed characteristics of TBLC specimens including the large airway and the impact on histological diagnostic rates of DPLD have not been investigated. METHODS: We retrospectively reviewed the specimen characteristics of patients with DPLD who underwent TBLC. RESULTS: Between February 2018 and January 2020, 74 patients and 177 specimens were included. There were 85 (48.0%) large airway specimens (LAS) that contained bronchial gland or bronchial cartilage. The ideal specimen ratio was significantly lower in the LAS-positive group than that in the LAS-negative group (5.8% vs. 45.6%), and the proportion of bronchioles, alveoli, and perilobular area were similarly lower in the LAS-positive group. The presence of traction bronchiectasis and diaphragm overlap sign on high-resolution computed tomography (HRCT) were also significantly higher in the LAS-positive group than those in the LAS-negative group. We observed a statistically significant trend in histological diagnostic yield (40.7% in LAS positive group; 60.8% in LAS positive and negative group; 91.6% in LAS negative group) (Cochran-Armitage trend test). CONCLUSION: LAS is a specimen often collected in TBLC and contains a low percentage of bronchioles, alveoli, and perilobular area. Since the histological diagnostic yield tends to be higher in cases that do not contain LAS, it may be important to determine the biopsy site that reduces the frequency of LAS collection by referring to the HRCT findings in TBLC.
Subject(s)
Bronchoscopy , Lung Diseases, Interstitial , Humans , Bronchoscopy/methods , Retrospective Studies , Lung Diseases, Interstitial/diagnosis , Lung Diseases, Interstitial/pathology , Lung/diagnostic imaging , Lung/pathology , Biopsy/methodsABSTRACT
Interaction cross sections for ^{42-51}Ca on a carbon target at 280 MeV/nucleon have been measured for the first time. The neutron number dependence of derived root-mean-square matter radii shows a significant increase beyond the neutron magic number N=28. Furthermore, this enhancement of matter radii is much larger than that of the previously measured charge radii, indicating a novel growth in neutron skin thickness. A simple examination based on the Fermi-type distribution, and mean field calculations point out that this anomalous enhancement of the nuclear size beyond N=28 results from an enlargement of the core by a sudden increase in the surface diffuseness of the neutron density distribution, which implies the swelling of the bare ^{48}Ca core in Ca isotopes beyond N=28.
ABSTRACT
BACKGROUND: Pulmonary alveolar proteinosis (PAP) is characterized by the accumulation of surfactant proteins within the alveolar spaces. Autoimmune PAP (APAP) caused by elevated levels of GM-CSF autoantibodies (GM-Ab) is very rarely associated with systemic autoimmune disease. Here we report a case of APAP manifested during immunosuppressive treatment for polymyositis with interstitial lung disease. CASE PRESENTATION: A 52-year-old woman treated at our hospital because of polymyositis with interstitial pneumonia had maintained remission by immunosuppressive treatment for 15 years. She had progressive dyspnea subsequently over several months with her chest CT showing ground-glass opacities (GGO) in bilateral geographic distribution. Her bronchoalveolar lavage fluid with cloudy appearance revealed medium-sized foamy macrophages and PAS-positive amorphous eosinophilic materials by cytological examination. We diagnosed her as APAP due to an increased serum GM-CSF autoantibody level. Attenuating immunosuppression failed to lead GGO improvement, but whole lung lavage (WLL) was effective in her condition. CONCLUSIONS: PAP should be considered as one of the differential diseases when the newly interstitial shadow was observed during immunosuppressive treatment. WLL should be regarded as the treatment option for APAP concurred in connective tissue disease (CTD).
Subject(s)
Autoantibodies/blood , Autoimmune Diseases/diagnosis , Lung Diseases, Interstitial/complications , Polymyositis/complications , Pulmonary Alveolar Proteinosis/diagnosis , Autoimmune Diseases/immunology , Autoimmune Diseases/physiopathology , Bronchoalveolar Lavage Fluid/cytology , Dyspnea/etiology , Female , Granulocyte-Macrophage Colony-Stimulating Factor/immunology , Humans , Immunosuppressive Agents/adverse effects , Lung/physiopathology , Lung Diseases, Interstitial/drug therapy , Middle Aged , Polymyositis/drug therapy , Pulmonary Alveolar Proteinosis/immunology , Pulmonary Alveolar Proteinosis/physiopathology , Pulmonary Alveolar Proteinosis/therapy , Tomography, X-Ray ComputedABSTRACT
Immunoglobulin G (IgG) is a major glycoprotein in ruminant colostrum. First day buffalo colostrum protein was purified on Sephadex G-100 and its mass was determined by MALDI-TOF as 147.848 KDa. The PMF data of protein subunits revealed its homology to IgG, which was supported by the identification of peptide sequences LLIYGATSR and VYNEYLPAPIVR corresponding to light and heavy chains of IgG by CID MS/MS analysis. The N-glycan microheterogeneity was established based on chemoselective glycoblotting technique with the identification of high mannose, neutral complex/hybrid and sialylated complex/hybrid glycans. A complete structural assignment of 54 N-linked oligosaccharides were identified and the ratio of sialyl oligosaccharides was found to be higher compared to neutral saccharides. The fucosylation observed in more than 20 oligosaccharides, high mannose and trisialyl oligosaccharides were present in diminutive amount. The high non-fucosyl and sialyl oligosaccharides in buffalo colostrum IgG provide ample scope for its utilization in targeted therapies to elicit effective ADCC and anti-inflammatory responses.
Subject(s)
Buffaloes/immunology , Colostrum/immunology , Immunoglobulin G/chemistry , Amino Acid Sequence , Animals , Chromatography, Liquid , Female , Glycosylation , Inflammation , Lactation , Mannose/chemistry , Molecular Sequence Data , Oligosaccharides/chemistry , Peptides/chemistry , Polysaccharides/chemistry , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Trypsin/chemistryABSTRACT
Environmental factors tend to influence the performance of individuals who exercise for extended periods. The present study aimed to determine energy metabolism while running in cold, wet conditions using a climatic chamber that can precisely simulate rainy conditions. 7 healthy men (age, 23.3±2.9 (SD) y; height, 168.6±7.5 cm; weight, 65.9±8.1 kg; V. O2max, 52.0±5.7 mL·kg - 1·min - 1) ran on a treadmill at 70% ËVO2max intensity for 30 min in a climatic chamber at an ambient temperature of 5°C in the presence (RAIN) or absence (CON) of 40 mm/h of precipitation. Expired air, esophageal temperature, heart rate, mean skin temperature, rating of perceived exertion and blood samples were measured. Esophageal temperature and mean skin temperature were significantly lower (P<0.05) in RAIN than in CON all. Minute ventilation, oxygen consumption and levels of plasma lactate and norepinephrine were significantly higher (P<0.05) in RAIN than in CON. In conclusion, the higher oxygen consumption and plasma lactate in RAIN indicated that energy demand increases when running in cold conditions.
Subject(s)
Energy Metabolism/physiology , Oxygen Consumption/physiology , Rain , Running/physiology , Adult , Body Temperature/physiology , Cold Temperature , Esophagus , Exercise Test/methods , Heart Rate/physiology , Humans , Lactic Acid/blood , Male , Norepinephrine/blood , Physical Exertion/physiology , Skin , Young AdultABSTRACT
Zucchini yellow mosaic virus (ZYMV) causes considerable losses of cucurbitaceous vegetables grown nearly all over the world; indeed, the commonly planted cultivars are highly susceptible to ZYMV. In all, 3 cultivars of American and 8 of European summer squash (Cucurbita pepo), and 6 Japanese and 21 European cucumber lines (Cucumis sativus), including both slicing and pickling species, were selected for the evaluation of their resistance to the most virulent Czech strain, ZYMV-H (GenBank accession number DQ144054). Butternut squash (Cucurbita moschata) 'Menina 15', Chinese slicing cucumber 'Taichung Mou Gua-1' (TMG-1), and watermelon (Citrullus lanatus) accession PI 595203 were included in the experiment, because they were reported to be resistant to ZYMV. The tested plants were mechanically inoculated by ZYMV-H and their resistance was assessed through a comparison of the relative virus protein concentrations and visual symptoms. Butternut squash Menina 15, Chinese slicing cucumber TMG-1, Japanese slicing cucumber breeds 'G22' and 'A192-18', and watermelon PI 595203 were evaluated as immune: the virus concentration in their leaves was zero, as verified by polymerase chain reaction. American summer squash 'Cougar' and Japanese slicing cucumber breeds 'A202-18', 'R10', and 'S93-18' were clearly resistant, because the virus multiplied at a low rate in these plants. The remaining tested cultivars were tolerant or susceptible to ZYMV.
Subject(s)
Fasciitis, Necrotizing/microbiology , Leg/microbiology , Lupus Erythematosus, Systemic/complications , Spondylitis/complications , Administration, Intravenous , Aged , Amputation, Surgical/methods , Anti-Bacterial Agents/therapeutic use , Bacterial Infections/microbiology , Bacterial Infections/pathology , Clindamycin/administration & dosage , Clindamycin/therapeutic use , Debridement/methods , Escherichia coli/isolation & purification , Fasciitis, Necrotizing/drug therapy , Fasciitis, Necrotizing/pathology , Fasciitis, Necrotizing/surgery , Female , Humans , Immunosuppressive Agents/therapeutic use , Leg/diagnostic imaging , Leg/pathology , Lupus Erythematosus, Systemic/drug therapy , Lupus Erythematosus, Systemic/pathology , Magnetic Resonance Imaging/methods , Meropenem , Spondylitis/diagnostic imaging , Spondylitis/microbiology , Spondylitis/pathology , Staphylococcus epidermidis/isolation & purification , Staphylococcus hominis/isolation & purification , Thienamycins/administration & dosage , Thienamycins/therapeutic use , Tomography, X-Ray Computed/methods , Treatment OutcomeABSTRACT
AIMS: The long-term physical health effects of the atomic bombings of Hiroshima and Nagasaki are well characterised, but the psychological effects remain unclear. Therefore, we sought to determine whether measures of exposure severity, as indirect measures of psychological trauma arising from exposure to the atomic bombings, are associated with suicide mortality among atomic bomb survivors. METHODS: The Life Span Study is a prospective cohort study of 93 741 Japanese atomic bomb survivors who were located within 10 km of the hypocentre in Hiroshima or Nagasaki at the time of the bombings in 1945, and 26 579 residents of Hiroshima and Nagasaki who were not in either city at the time of the bombings, matched to survivors on city, sex and age. Measures of exposure severity included: proximity to the hypocentre, type of shielding between the survivor and the blast and self-reported occurrence of acute radiation and thermal injuries. Date of death was obtained from the Japanese National Family Registry system. Cause of death was obtained from death certificates. Adjusted hazard ratios (HRs) were estimated from Cox regression models overall and stratified by sex and age. RESULTS: During the 60-year follow-up period (1950-2009), 1150 suicide deaths were recorded among 120 231 participants (23.6 per 100 000 person-years): 510 among 70 092 women (17.2 per 100 000 person-years) and 640 among 50 139 men (33.6 per 100 000 person-years). Overall, there was no association of proximity, type of shielding or the occurrence of acute injuries with suicide mortality. Among those <25 years of age at the time of the bombings, increased suicide risk was observed for survivors outside v. shielded inside any structure (HR: 1.24; 95% confidence interval (CI): 1.03, 1.48; interaction p = 0.054) and for those who reported flash burns (HR: 1.32; 95% CI: 1.00, 1.73; interaction p = 0.025). Sex-stratified analyses indicated that these associations were limited to men. Among women, closer proximity to the hypocentre was associated with a non-significant increase in suicide risk, with a positive association between proximity and suicide risk observed among women <15 years of age (HR: 1.09 per km; 95% CI: 1.00, 1.18; interaction p = 0.067). CONCLUSIONS: Proximity to the hypocentre, shielding and acute injury presence do not generally appear to influence suicide mortality among atomic bomb survivors. However, heterogeneity may exist by age and sex, with younger survivors potentially more sensitive to psychological trauma. Coupled with other studies, our results suggest the importance of long-term monitoring of mental health among young populations exposed to catastrophic events or mass trauma.
Subject(s)
Neoplasms, Radiation-Induced , Nuclear Weapons , Suicide , Female , Humans , Japan/epidemiology , Male , Prospective Studies , SurvivorsABSTRACT
T cells with T cell receptor (TCR) transgenes that recognized CD1 on syngeneic B cells stimulated B cells to secrete immunoglobulins in vitro. The CD4+, CD8+, or CD4-CD8- T cells from the spleen of the TCR transgenic BALB/c donors induced lupus with anti-double stranded DNA antibodies, proteinuria, and immune complex glomerulonephritis in irradiated BALB/c nude mice reconstituted with nude bone marrow. Injection of purified CD4-CD8- T cells from the marrow of transgenic donors prevented the induction of lupus by the transgenic T cells. Transgenic T cells that induced lupus secreted large amounts of interferon (IFN)-gamma and little interleukin (IL)-4, and those that prevented lupus secreted large amounts of IL-4 and little IFN-gamma or IL-10.
Subject(s)
Antigens, CD1/immunology , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Cytokines/physiology , Lupus Erythematosus, Systemic/immunology , Animals , Bone Marrow Cells/immunology , Cytokines/metabolism , Disease Models, Animal , Interferon-gamma/metabolism , Interleukin-4/metabolism , Lupus Erythematosus, Systemic/etiology , Mice , Mice, Inbred BALB C , Mice, Nude , Mice, Transgenic , Receptors, Antigen, T-Cell, alpha-beta/biosynthesisABSTRACT
It is widely accepted that actin filaments and the conventional double-headed myosin interact to generate force for many types of nonmuscle cell motility, and that this interaction occurs when the myosin regulatory light chain (MLC) is phosphorylated by MLC kinase (MLCK) together with calmodulin and Ca(2+). However, recent studies indicate that Rho-kinase is also involved in regulating the smooth muscle and nonmuscle cell contractility. We have recently isolated reactivatable stress fibers from cultured cells and established them as a model system for actomyosin-based contraction in nonmuscle cells. Here, using isolated stress fibers, we show that Rho-kinase mediates MLC phosphorylation and their contraction in the absence of Ca(2+). More rapid and extensive stress fiber contraction was induced by MLCK than was by Rho-kinase. When the activity of Rho-kinase but not MLCK was inhibited, cells not only lost their stress fibers and focal adhesions but also appeared to lose cytoplasmic tension. Our study suggests that actomyosin-based nonmuscle contractility is regulated by two kinase systems: the Ca(2+)-dependent MLCK and the Rho-kinase systems. We propose that Ca(2+) is used to generate rapid contraction, whereas Rho-kinase plays a major role in maintaining sustained contraction in cells.
Subject(s)
Contractile Proteins/metabolism , Movement/physiology , Protein Serine-Threonine Kinases/metabolism , Stress Fibers/physiology , rho GTP-Binding Proteins/metabolism , Calcium/metabolism , Cell Fractionation/methods , Cell-Free System , Fibroblasts/cytology , Glycerol/pharmacology , Humans , Intracellular Signaling Peptides and Proteins , Male , Models, Biological , Myosin Light Chains/metabolism , Myosin-Light-Chain Kinase/metabolism , Octoxynol/pharmacology , Phosphorylation , Protein Serine-Threonine Kinases/antagonists & inhibitors , Stress Fibers/drug effects , rho-Associated KinasesABSTRACT
The ezrin/radixin/moesin (ERM) proteins are involved in actin filament/plasma membrane interaction that is regulated by Rho. We examined whether ERM proteins are directly phosphorylated by Rho-associated kinase (Rho-kinase), a direct target of Rho. Recombinant full-length and COOH-terminal half radixin were incubated with constitutively active catalytic domain of Rho-kinase, and approximately 30 and approximately 100% of these molecules, respectively, were phosphorylated mainly at the COOH-terminal threonine (T564). Next, to detect Rho-kinase-dependent phosphorylation of ERM proteins in vivo, we raised a mAb that recognized the T564-phosphorylated radixin as well as ezrin and moesin phosphorylated at the corresponding threonine residue (T567 and T558, respectively). Immunoblotting of serum-starved Swiss 3T3 cells with this mAb revealed that after LPA stimulation ERM proteins were rapidly phosphorylated at T567 (ezrin), T564 (radixin), and T558 (moesin) in a Rho-dependent manner and then dephosphorylated within 2 min. Furthermore, the T564 phosphorylation of recombinant COOH-terminal half radixin did not affect its ability to bind to actin filaments in vitro but significantly suppressed its direct interaction with the NH2-terminal half of radixin. These observations indicate that the Rho-kinase-dependent phosphorylation interferes with the intramolecular and/ or intermolecular head-to-tail association of ERM proteins, which is an important mechanism of regulation of their activity as actin filament/plasma membrane cross-linkers.
Subject(s)
Blood Proteins/metabolism , Cytoskeletal Proteins , Membrane Proteins/metabolism , Microfilament Proteins , Phosphoproteins/metabolism , Phosphothreonine/metabolism , Protein Serine-Threonine Kinases/metabolism , Proteins/metabolism , 3T3 Cells , Actins/metabolism , Animals , Antibodies, Monoclonal , Blood Proteins/chemistry , Blood Proteins/immunology , Cell Membrane/metabolism , Immunoblotting , Intracellular Signaling Peptides and Proteins , Membrane Proteins/chemistry , Membrane Proteins/immunology , Mice , Phosphoproteins/chemistry , Phosphorylation , Proteins/chemistry , Recombinant Proteins/metabolism , rho-Associated KinasesABSTRACT
Rho-associated kinase (Rho-kinase), which is activated by the small GTPase Rho, regulates formation of stress fibers and focal adhesions, myosin fiber organization, and neurite retraction through the phosphorylation of cytoskeletal proteins, including myosin light chain, the ERM family proteins (ezrin, radixin, and moesin) and adducin. Rho-kinase was found to phosphorylate a type III intermediate filament (IF) protein, glial fibrillary acidic protein (GFAP), exclusively at the cleavage furrow during cytokinesis. In the present study, we examined the roles of Rho-kinase in cytokinesis, in particular organization of glial filaments during cytokinesis. Expression of the dominant-negative form of Rho-kinase inhibited the cytokinesis of Xenopus embryo and mammalian cells, the result being production of multinuclei. We then constructed a series of mutant GFAPs, where Rho-kinase phosphorylation sites were variously mutated, and expressed them in type III IF-negative cells. The mutations induced impaired segregation of glial filament (GFAP filament) into postmitotic daughter cells. As a result, an unusually long bridge-like cytoplasmic structure formed between the unseparated daughter cells. Alteration of other sites, including the cdc2 kinase phosphorylation site, led to no remarkable defect in glial filament separation. These results suggest that Rho-kinase is essential not only for actomyosin regulation but also for segregation of glial filaments into daughter cells which in turn ensures correct cytokinetic processes.
Subject(s)
Cell Division/genetics , Cell Division/physiology , Protein Serine-Threonine Kinases/genetics , Protein Serine-Threonine Kinases/physiology , Amino Acid Sequence , Animals , Catalytic Domain/genetics , Cytoskeleton/metabolism , Cytoskeleton/ultrastructure , Female , Glial Fibrillary Acidic Protein/metabolism , Intermediate Filaments/metabolism , Intermediate Filaments/ultrastructure , Intracellular Signaling Peptides and Proteins , L Cells , Mice , Molecular Sequence Data , Mutagenesis, Site-Directed , Mutation , Phosphorylation , Transfection , Xenopus , rho-Associated KinasesABSTRACT
Rho-associated kinase (Rho-kinase), which is activated by the small GTPase Rho, phosphorylates myosin-binding subunit (MBS) of myosin phosphatase and thereby inactivates the phosphatase activity in vitro. Rho-kinase is thought to regulate the phosphorylation state of the substrates including myosin light chain (MLC), ERM (ezrin/radixin/moesin) family proteins and adducin by their direct phosphorylation and by the inactivation of myosin phosphatase. Here we identified the sites of phosphorylation of MBS by Rho-kinase as Thr-697, Ser-854 and several residues, and prepared antibody that specifically recognized MBS phosphorylated at Ser-854. We found by use of this antibody that the stimulation of MDCK epithelial cells with tetradecanoylphorbol-13-acetate (TPA) or hepatocyte growth factor (HGF) induced the phosphorylation of MBS at Ser-854 under the conditions in which membrane ruffling and cell migration were induced. Pretreatment of the cells with Botulinum C3 ADP-ribosyltransferase (C3), which is thought to interfere with Rho functions, or Rho-kinase inhibitors inhibited the TPA- or HGF-induced MBS phosphorylation. The TPA stimulation enhanced the immunoreactivity of phosphorylated MBS in the cytoplasm and membrane ruffling area of MDCK cells. In migrating MDCK cells, phosphorylated MBS as well as phosphorylated MLC at Ser-19 were localized in the leading edge and posterior region. Phosphorylated MBS was localized on actin stress fibers in REF52 fibroblasts. The microinjection of C3 or dominant negative Rho-kinase disrupted stress fibers and weakened the accumulation of phosphorylated MBS in REF52 cells. During cytokinesis, phosphorylated MBS, MLC and ERM family proteins accumulated at the cleavage furrow, and the phosphorylation level of MBS at Ser-854 was increased. Taken together, these results indicate that MBS is phosphorylated by Rho-kinase downstream of Rho in vivo, and suggest that myosin phosphatase and Rho-kinase spatiotemporally regulate the phosphorylation state of Rho-kinase substrates including MLC and ERM family proteins in vivo in a cooperative manner.
Subject(s)
Myosins/metabolism , Phosphoprotein Phosphatases/metabolism , Protein Serine-Threonine Kinases/metabolism , Actins/metabolism , Amino Acid Sequence , Animals , Cell Division/physiology , Cell Line , Cell Movement/physiology , Dogs , Intracellular Signaling Peptides and Proteins , Membrane Proteins/metabolism , Molecular Sequence Data , Myosin Light Chains/metabolism , Myosin-Light-Chain Phosphatase , Neurofibromin 2 , Peptides/metabolism , Phosphoprotein Phosphatases/analysis , Phosphorylation , Sequence Alignment , rho-Associated KinasesABSTRACT
The small guanosine triphosphatase (GTPase) Rho is implicated in the formation of stress fibers and focal adhesions in fibroblasts stimulated by extracellular signals such as lysophosphatidic acid (LPA). Rho-kinase is activated by Rho and may mediate some biological effects of Rho. Microinjection of the catalytic domain of Rho-kinase into serum-starved Swiss 3T3 cells induced the formation of stress fibers and focal adhesions, whereas microinjection of the inactive catalytic domain, the Rho-binding domain, or the pleckstrin-homology domain inhibited the LPA-induced formation of stress fibers and focal adhesions. Thus, Rho-kinase appears to mediate signals from Rho and to induce the formation of stress fibers and focal adhesions.
Subject(s)
Actins/metabolism , Cell Adhesion , Protein Serine-Threonine Kinases/metabolism , 3T3 Cells , Adenosine Triphosphate/metabolism , Animals , Binding Sites , Cell Line , DNA, Complementary/genetics , Enzyme Inhibitors/pharmacology , GTP Phosphohydrolases/metabolism , Intracellular Signaling Peptides and Proteins , Lysophospholipids/pharmacology , Mice , Mutation , Protein Serine-Threonine Kinases/antagonists & inhibitors , Protein Serine-Threonine Kinases/genetics , Recombinant Fusion Proteins/metabolism , Staurosporine/pharmacology , rho-Associated KinasesABSTRACT
Rho, a Ras-like small guanosine triphosphatase, has been implicated in cytoskeletal responses to extracellular signals such as lysophosphatidic acid (LPA) to form stress fibers and focal contacts. The form of RhoA bound to guanosine triphosphate directly bound to and activated a serine-threonine kinase, protein kinase N (PKN). Activated RhoA formed a complex with PKN and activated it in COS-7 cells. PKN was phosphorylated in Swiss 3T3 cells stimulated with LPA, and this phosphorylation was blocked by treatment of cells with botulinum C3 exoenzyme. Activation of Rho may be linked directly to a serine-threonine kinase pathway.
Subject(s)
Botulinum Toxins , GTP Phosphohydrolases/metabolism , GTP-Binding Proteins/metabolism , Protein Kinase C/metabolism , 3T3 Cells , ADP Ribose Transferases/pharmacology , Amino Acid Sequence , Animals , Cell Line , Chromatography, Affinity , Enzyme Activation , Guanosine Triphosphate/metabolism , Lysophospholipids/pharmacology , Mice , Molecular Sequence Data , Phosphorylation , Recombinant Fusion Proteins/metabolism , rhoA GTP-Binding ProteinABSTRACT
The small guanosine triphosphatase Rho is implicated in myosin light chain (MLC) phosphorylation, which results in contraction of smooth muscle and interaction of actin and myosin in nonmuscle cells. The guanosine triphosphate (GTP)-bound, active form of RhoA (GTP.RhoA) specifically interacted with the myosin-binding subunit (MBS) of myosin phosphatase, which regulates the extent of phosphorylation of MLC. Rho-associated kinase (Rho-kinase), which is activated by GTP.RhoA, phosphorylated MBS and consequently inactivated myosin phosphatase. Overexpression of RhoA or activated RhoA in NIH 3T3 cells increased phosphorylation of MBS and MLC. Thus, Rho appears to inhibit myosin phosphatase through the action of Rho-kinase.
Subject(s)
GTP Phosphohydrolases/metabolism , GTP-Binding Proteins/metabolism , Phosphoprotein Phosphatases/antagonists & inhibitors , Protein Serine-Threonine Kinases/metabolism , 3T3 Cells , Actins/metabolism , Amino Acid Sequence , Animals , Cattle , Intracellular Signaling Peptides and Proteins , Isopropyl Thiogalactoside/pharmacology , Marine Toxins , Mice , Molecular Sequence Data , Muscle Contraction , Muscle, Smooth/physiology , Myosin Light Chains/metabolism , Myosin-Light-Chain Phosphatase , Oxazoles/pharmacology , Phosphoprotein Phosphatases/metabolism , Phosphorylation , rho-Associated Kinases , rhoA GTP-Binding ProteinABSTRACT
OBJECTIVE: Mice selected for a strong (AIRmax) or weak (AIRmin) acute inflammatory response present different susceptibilities to bacterial infections, autoimmune diseases and carcinogenesis. Variations in these phenotypes have been also detected in AIRmax and AIRmin mice rendered homozygous for Slc11a1 resistant (R) and susceptible (S) alleles. Our aim was to investigate if the phenotypic differences observed in these mice was related to the complement system. MATERIAL: AIRmax and AIRmin mice and AIRmax and AIRmin groups homozygous for the resistance (R) or susceptibility (S) alleles of the solute carrier family 11a1 member (Slc11a1) gene, formerly designated Nramp-1. METHODS AND RESULTS: While no difference in complement activity was detected in sera from AIRmax and AIRmin strains, all sera from AIRmax Slc11a1 resistant mice (AIRmax(RR)) presented no complement-dependent hemolytic activity. Furthermore, C5 was not found in their sera by immunodiffusion and, polymerase chain reaction and DNA sequencing of its gene demonstrated that AIRmax(RR) mice are homozygous for the C5 deficient (D) mutation previously described in A/J. Therefore, the C5D allele was fixed in homozygosis in AIRmax(RR) line. CONCLUSIONS: The AIRmax(RR) line is a new experimental mouse model in which a strong inflammatory response can be triggered in vivo in the absence of C5.
Subject(s)
Complement C5 , Inflammation/genetics , Mice, Inbred Strains , Animals , Cation Transport Proteins/genetics , Cation Transport Proteins/immunology , Complement Activation , Complement C5/genetics , Complement C5/immunology , Complement Pathway, Alternative/immunology , Female , Genetic Predisposition to Disease , Hemolysis , Inflammation/immunology , Male , Mice , Mice, Inbred Strains/genetics , Mice, Inbred Strains/immunologyABSTRACT
We identified a 4-year-old Brazilian boy from a family of Japanese descent and history of consanguinity, who suffered from severe recurrent pneumonia. He carries factor H (FH) deficiency associated with reduced levels of component C9 and low serum levels of C3 and factor B. His mother also presented low levels of these proteins and factor I, while his father and sister had only lower levels of FH. Western blot assays confirmed the complete absence of FH and FHL-1 polypeptides in this patient. Sequencing of the proband's FH cDNA revealed a homozygous G453A substitution, encoding an Arg(127)His change. His mother, father and sister are heterozygous for this substitution. Despite the absence of FH in the plasma, this protein was detected in the patient's fibroblasts, suggesting that Arg(127) may be important for FH secretion. Low concentrations of C9 were detected in the proband serum but no mutations in the patient's C9 gene or promoter have been identified, suggesting that this is a consequence of uncontrolled complement activation and high C9 consumption.
Subject(s)
Blood Coagulation Disorders, Inherited/blood , Blood Coagulation Disorders, Inherited/genetics , Complement C9/analysis , Complement Factor H/deficiency , Complement Factor H/genetics , Base Sequence , Blood Coagulation Disorders, Inherited/physiopathology , Blotting, Western , Child, Preschool , Complement Activation/physiology , Complement C3b Inactivator Proteins , Complement C9/genetics , Complement System Proteins/analysis , Consanguinity , Enzyme-Linked Immunosorbent Assay , Female , Fibroblasts/metabolism , Humans , Male , Microscopy, Confocal , Mutation , Pedigree , Pneumonia/etiology , Reverse Transcriptase Polymerase Chain ReactionABSTRACT
In cultured hippocampal neurons, one axon and several dendrites differentiate from a common immature process. Here we found that CRMP-2/TOAD-64/Ulip2/DRP-2 (refs. 2-4) level was higher in growing axons of cultured hippocampal neurons, that overexpression of CRMP-2 in the cells led to the formation of supernumerary axons and that expression of truncated CRMP-2 mutants suppressed the formation of primary axon in a dominant-negative manner. Thus, CRMP-2 seems to be critical in axon induction in hippocampal neurons, thereby establishing and maintaining neuronal polarity.
Subject(s)
Cell Differentiation/genetics , Cell Size/genetics , Cells, Cultured/metabolism , Growth Cones/metabolism , Hippocampus/embryology , Nerve Tissue Proteins/genetics , Animals , Cells, Cultured/cytology , Dendrites/metabolism , Dendrites/ultrastructure , GAP-43 Protein/metabolism , Growth Cones/ultrastructure , Hippocampus/cytology , Hippocampus/metabolism , Immunohistochemistry , Intercellular Signaling Peptides and Proteins , Microtubule-Associated Proteins/metabolism , Mutation/physiology , Nerve Tissue Proteins/deficiency , Synapsins/metabolism , Synaptophysin/metabolism , Transfection , tau Proteins/metabolismABSTRACT
OBJECTIVE: Vascular endothelial growth factor (VEGF) is one of the most potent endothelial cell mitogens and plays a critical role in angiogenesis of endometrial carcinomas. Several studies have demonstrated positive associations between VEGF gene polymorphisms and several carcinomas. In this study we investigated whether VEGF gene polymorphisms are associated with endometrial carcinomas in a Japanese population. METHODS: The allele frequencies and genotype distributions of VEGF -460 C/T, +405 G/C, and +936 C/T polymorphisms were examined in 105 endometrial carcinomas and 179 controls using PCR-RFLP analysis. An association of these polymorphisms with three-year disease-free survival was evaluated using the Kaplan-Meier method. RESULTS: No significant differences in the allele frequencies and genotype distributions of VEGF -460 C/T (p = 0.54, 0.90), +405 G/C (p = 0.31, 0.17), and +936 C/T polymorphisms (p = 0.46, 0.24) were observed between endometrial carcinoma patients and controls. There were no significant differences in the frequencies of haplotype -460 T/+405 C between patients and controls. Futhermore, VEGF -460 C/T, +405 G/C, and +936 C/T polymorphisms were not associated with three-year disease-free survival of endometrial carcinoma patients. CONCLUSIONS: Although limited by sample size, our study did not demonstrated any evidence that VEGF -460 C/T, +405 G/C, and +936 C/T polymorphisms are associated with an increased risk of endometrial carcinomas in Japanese women.