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1.
Br J Dermatol ; 185(6): 1209-1220, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34254298

RESUMO

BACKGROUND: Behçet disease (BD) presents with lymphocytic and neutrophilic vasculitis of unknown aetiology. HLA-B*51, the endoplasmic reticulum aminopeptidase 1 (ERAP1), and interleukin 23 receptor (IL23R)/IL12R are genetic risk factors. IL-23 regulates IL-17A, which controls the recruitment and activation of neutrophils. OBJECTIVES: To determine pathological changes in BD skin lesions related to the complex genetic predisposition. METHODS: We characterized the expression of IL-17A and IL-23A in various cell types by immunohistological double staining of sections from papulopustular skin lesions of acute attacks of BD and psoriasis vulgaris lesions, another HLA-class I-associated T-cell-mediated autoimmune disease in which excessive T-cell-derived IL-17A production promotes neutrophil activation. RESULTS: We found that in BD lesions, as in psoriasis, actively expanding CD8+ T cells were the predominant source of IL-17A. IL-17A+ CD8+ T (Tc 17) cells outnumbered infiltrating IL-17A+ CD4+ T cells. Unlike the epidermal localization of CD8+ T cells in psoriasis, Tc 17 cells in BD lesions mainly infiltrated the perivascular tissue and the blood vessel walls of dermis and subcutaneous tissue. They co-localised with a marked IL-23A expression by CD11c+ dendritic cells and CD68+ macrophages. IL-17A expression was associated with extensive recruitment of neutrophils around blood vessels that formed neutrophil extracellular traps (NETs). CONCLUSIONS: In BD, the genetic predisposition may mediate antigen-specific activation and differentiation of a Tc 17 response, possibly targeting endothelial (auto)antigens. Neutrophils recruited by IL-17A in this process may enhance tissue damage by extensive NET formation (NETosis). Thus, the IL-23/IL-17 axis presumably controls neutrophilic inflammation in BD vasculitis in the context of a predominant antigen-specific CD8+ T-cell response.


Assuntos
Síndrome de Behçet , Armadilhas Extracelulares , Psoríase , Aminopeptidases/metabolismo , Autoimunidade , Síndrome de Behçet/patologia , Linfócitos T CD8-Positivos , Humanos , Antígenos de Histocompatibilidade Menor/metabolismo
2.
Tech Coloproctol ; 23(3): 251-257, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30838463

RESUMO

BACKGROUND: Although complete mesocolic excision has been performed for 10 years there remains no published prospective data. The lack of a classification which includes completeness of mesocolic tissue removal as well as plane of surgery contributes to the problem of comparing studies. The aim of the present study was to develop such a classification for right hemicolectomy. METHODS: In a prospective, non-randomized trial we collected specimens of right hemicolectomies from 38 German hospitals between February 2012 and October 2016. The degree of radicality of resection was reported. Photographs were taken of the specimens. After screening the images it became apparent that the specimens could be divided into four main groups according to the degree of missing mesocolic tissue, and three subgroups reflecting the plane of surgery. RESULTS: Of 1373 patients 1097 images were available. Grading was possible in 1077 (98.2%). Distribution was Type 0 (best) 38.6%, Type I 43.3%, Type II 8.5%, Type III (poorest) 7.8%. Surgery was considered to be in a suboptimal plane of surgery in 15.2% overall, highest in Type III (37%) and lowest in Type 0 (7.8%, p < 0.001). CONCLUSIONS: The proposed classification may be a relevant tool for the further investigation of CME for right colon cancer because it allows us to differentiate the aspects of lymphadenectomy and the preservation of the integrity of the mesocolon.


Assuntos
Colectomia/classificação , Neoplasias do Colo/cirurgia , Mesocolo/cirurgia , Idoso , Idoso de 80 Anos ou mais , Colectomia/métodos , Neoplasias do Colo/patologia , Feminino , Humanos , Excisão de Linfonodo/classificação , Excisão de Linfonodo/métodos , Masculino , Pessoa de Meia-Idade , Ensaios Clínicos Controlados não Aleatórios como Assunto , Estudos Prospectivos
3.
Org Biomol Chem ; 13(20): 5734-42, 2015 May 28.
Artigo em Inglês | MEDLINE | ID: mdl-25902412

RESUMO

Triplexes with a gap in the purine strand have been shown to bind adenosine or guanosine derivatives through a combination of Watson-Crick and Hoogsteen base pairing. Rigidifying the binding site should be advantageous for affinity. Here we report that clamps delimiting the binding site have a modest effect on affinity, while bridging the gap of the purine strand can strongly increase affinity for ATP, cAMP, and FAD. The lowest dissociation constants were measured for two-strand triple helical motifs with a propylene bridge or an abasic nucleoside analog, with Kd values as low as 30 nM for cAMP in the latter case. Taken together, our data suggest that improving preorganization through covalent bridges increases the affinity for nucleotide ligands. But, a bulky bridge may also block one of two alternative binding modes for the adenine base. The results may help to design new receptors, switches, or storage motifs for purine-containing ligands.


Assuntos
Adenina/metabolismo , Trifosfato de Adenosina/metabolismo , AMP Cíclico/metabolismo , DNA/química , DNA/metabolismo , Flavina-Adenina Dinucleotídeo/metabolismo , Purinas/química , Adenina/química , Motivos de Aminoácidos , Pareamento de Bases , Sítios de Ligação , Humanos , Ligação de Hidrogênio , Modelos Moleculares , Conformação de Ácido Nucleico , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Termodinâmica
4.
Artigo em Inglês | MEDLINE | ID: mdl-21995181

RESUMO

BACKGROUND: Genetically determined defects in epidermal skin barrier function may contribute to the development of irritant and/or allergic contact dermatitis in chronic hand eczema (CHE). OBJECTIVES: To assess whether a deletion in the late cornified envelope genes LCE3B and LCE3C may constitute a genetic predisposition for the development of CHE or any of its subtypes. PATIENTS AND METHODS: A total of 153 German patients with clearly defined CHE subtypes and 268 healthy individuals were screened for the deletion LCE3C_LCE3B-del by allele-specific polymerase chain reaction. RESULTS: Classification of the patients by etiologic subtypes revealed an association between the LCE3C_LCE3B-del allele and CHE due to allergic contact dermatitis. In this subtype, 19/37 patients (51.4%) were homozygous deletion carriers, 11/37 (29.7%) were heterozygous carriers, and just 7/37 (18.9%) were wild-type individuals. Compared to the other CHE subgroups and the healthy control group (homozygous, 88/268 [32.83%]; heterozygous, 133/268 [49.63%]; and wild-type, 47/268 [17.54%]), the prevalence of LCE3C_LCE3B-del in these patients reached statistical significance (P = .03977), as did homozygous deletion carrier status (P = .01044 for other subtypes and P = .02695 for controls). CONCLUSIONS: A deletion of LCE genes may promote the development of allergic contact dermatitis, which is a form of CHE involving delayed-type hypersensitivity.


Assuntos
Proteínas Ricas em Prolina do Estrato Córneo/genética , Dermatite Alérgica de Contato/genética , Deleção de Genes , Predisposição Genética para Doença/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Alelos , Doença Crônica , Dermatite Alérgica de Contato/patologia , Feminino , Genótipo , Mãos/patologia , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Adulto Jovem
5.
Br J Dermatol ; 161(4): 801-7, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19538184

RESUMO

BACKGROUND: The pathogenesis of chronic hand eczema (CHE) is multifactorial and involves both endogenous predisposition and environmental triggers. OBJECTIVES: Filaggrin is a structural protein of the cornified envelope and important for the formation of the epidermal skin barrier. The aim of this investigation was to evaluate the role of mutations in the filaggrin gene (FLG) in the development of CHE. METHODS: In total, 122 German patients with clearly defined CHE subtypes were screened for the FLG variants R501X and 2282del4 by polymerase chain reaction and restriction enzyme digest analysis. The prevalence of these variants in CHE patients was compared with that in 95 healthy individuals. RESULTS: Overall, allele frequency and the number of mutation carriers were similar in both the CHE and control groups. When classified according to clearly defined CHE subtypes, however, the nonfunctional FLG variants showed an association with CHE involving an aetiological combination of contact allergy and irritant factors [P = 0.04; P (exact test) = 0.06; P (difference in rates) = 0.09; 95% confidence interval (CI) 0-56.8)], or with excessive daily exposure to water and irritants [P = 0.003; P (difference in rates) < 0.001; 95% CI 29.3-67.9]. CONCLUSION: Heterozygosity for nonfunctional mutations in the FLG gene may contribute to the manifestation and maintenance of a particular CHE subtype that is characterized by the combination of allergic and irritant contact dermatitis.


Assuntos
Dermatite Alérgica de Contato/genética , Dermatite Irritante/genética , Predisposição Genética para Doença/genética , Dermatoses da Mão/genética , Proteínas de Filamentos Intermediários/genética , Mutação/genética , Adulto , Idoso , Doença Crônica , Dermatite Alérgica de Contato/patologia , Dermatite Irritante/patologia , Feminino , Proteínas Filagrinas , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Fenótipo , Adulto Jovem
6.
Science ; 241(4865): 570-3, 1988 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-2840740

RESUMO

The mating-type alleles A and a of Neurospora crassa control mating in the sexual cycle and function in establishing heterokaryon incompatibility in the vegetative cycle. The A and a alleles were cloned, and they were shown to encode both the sexual functions and vegetative incompatibility. The mating-type clones contain nonhomologous DNA segments that are flanked by common DNA sequences. Neurospora crassa and all heterothallic and pseudohomothallic Neurospora species contain a single copy of one mating-type sequence or the other within each haploid genome. The six known self-fertile homothallic isolates contain an A homolog, but only one species also contains a homologous sequences. Homothallism in these species is not due to mating-type switching, as it is in Saccharomyces cerevisiae.


Assuntos
DNA Fúngico , Genes Fúngicos , Genes Fúngicos Tipo Acasalamento , Neurospora crassa/genética , Neurospora/genética , Peptídeos/genética , Mapeamento Cromossômico , Enzimas de Restrição do DNA/genética , Fator de Acasalamento
7.
Maturitas ; 91: 8-18, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-27451316

RESUMO

BACKGROUND: The severe burden imposed by frailty and disability in old age is a major challenge for healthcare systems in low- and middle-income countries alike. The current study aimed to provide estimates of the prevalence of frailty and disability in older adult populations and to examine their relationship with socioeconomic factors in six countries. METHODS: Focusing on adults aged 50+ years, a frailty index was constructed as the proportion of deficits in 40 variables, and disability was assessed using the World Health Organization Disability Assessment Schedule (WHODAS 2.0), as part of the Study on global AGEing and adult health (SAGE) Wave 1 in China, Ghana, India, Mexico, Russia and South Africa. RESULTS: This study included a total of 34,123 respondents. China had the lowest percentages of older adults with frailty (13.1%) and with disability (69.6%), whereas India had the highest percentages (55.5% and 93.3%, respectively). Both frailty and disability increased with age for all countries, and were more frequent in women, although the sex gap varied across countries. Lower levels of both frailty and disability were observed at higher levels of education and wealth. Both education and income were protective factors for frailty and disability in China, India and Russia, whereas only income was protective in Mexico, and only education in South Africa. CONCLUSIONS: Age-related frailty and disability are increasing concerns for older adult populations in low- and middle-income countries. The results indicate that lower levels of frailty and disability can be achieved for older people, and the study highlights the need for targeted preventive approaches and support programs.


Assuntos
Doença Crônica/epidemiologia , Pessoas com Deficiência/estatística & dados numéricos , Idoso , Idoso de 80 Anos ou mais , Países em Desenvolvimento , Avaliação da Deficiência , Feminino , Saúde Global , Serviços de Saúde para Idosos , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Fatores de Risco , Fatores Socioeconômicos , Organização Mundial da Saúde
8.
Biochim Biophys Acta ; 1205(1): 83-8, 1994 Mar 16.
Artigo em Inglês | MEDLINE | ID: mdl-8142488

RESUMO

Creatine kinase modified by S-methyl methanethiosulfonate and devoid of reactive thiol group has been reported to retain about 18-40% of the activity of the native enzyme. It has now been found that during the reaction catalyzed by the modified enzyme the rate increases with time and if the reaction is allowed to continue sufficiently long, the enzyme eventually recovers full activity. The presence of substrates is not required for the reactivation as suitable dilution after removal of MMTS in excess leads to complete reactivation of the MMTS modified enzyme with the simultaneous regeneration of reactive thiol per each dimeric molecule as shown by determinations with DTNB and IAN. The addition of MMTS during the course of reactivation again inactivates the reactivated enzyme. The activity recovery is therefore due to the regeneration of reactive thiol and it appears that the active-site thiols are essential for the activity of rabbit muscle creatine kinase.


Assuntos
Creatina Quinase/antagonistas & inibidores , Metanossulfonato de Metila/análogos & derivados , Compostos de Sulfidrila/análise , Animais , Sítios de Ligação , Creatina Quinase/química , Ácido Ditionitrobenzoico/farmacologia , Ativação Enzimática , Metanossulfonato de Metila/farmacologia , Músculos/enzimologia , Coelhos
9.
Biochim Biophys Acta ; 1524(1): 75-85, 2001 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-11078961

RESUMO

The leukocyte adhesion molecule L-selectin, which mediates the initial steps of leukocyte attachment to vascular endothelium, is intensely glycosylated. Different glycoforms of L-selectin are expressed on different leukocyte subsets and differences in L-selectin glycosylation appear to be correlated with the leukocyte's ability to attach to different endothelial targets. In the present study we addressed the question whether glycosylation of L-selectin influences L-selectin-ligand interactions. To obtain different glycoforms of L-selectin, recombinant proteins were expressed both in the baby hamster kidney (BHK) cell line and in the human myelogenous cell line K562, resulting in sL-sel[BHK] or sL-sel[K562], respectively. The glycosylation characteristics of the purified proteins were determined. The most striking differences in glycosylation were seen in the terminal sialylation. Each of the two proteins carried sialic acids in the alpha 2-3 position, while alpha 2-6-bound sialic acids were found exclusively on sL-sel[K562]. To investigate their adhesive properties, both recombinant sL-selectins were used in cell adhesion assays and interactions with the ligands present on various hematopoietic cell lines or activated human cardiac microvascular endothelial cells were examined. The binding capacity of sL-sel[K562] was about 1.6 fold higher compared to sL-sel[BHK] under static as well as under flow conditions. These findings indicate that the terminal sialylation pattern of L-selectin modulates its binding characteristics.


Assuntos
Adesivos/química , Endotélio Vascular/química , Células-Tronco Hematopoéticas/química , Selectina L/química , Amidoidrolases , Adesão Celular , Linhagem Celular , Citometria de Fluxo , Glicosilação , Humanos , Selectina L/biossíntese , Selectina L/isolamento & purificação , Ligantes , Peptídeo-N4-(N-acetil-beta-glucosaminil) Asparagina Amidase , Ligação Proteica , Proteínas Recombinantes/química , Proteínas Recombinantes/isolamento & purificação , Solubilidade , Transfecção
10.
Protein Sci ; 1(5): 678-87, 1992 May.
Artigo em Inglês | MEDLINE | ID: mdl-1304366

RESUMO

The bifunctional reagent 1,4-dibromobutanedione (DBBD) reacts covalently with pyruvate kinase from rabbit muscle to cause inactivation of the enzyme at a rate that is linearly dependent on the reagent concentration, giving a second order rate constant of 444 min-1 M-1. The individual substrates phosphoenolpyruvate (with KCl), ADP, or ATP in the presence of divalent metal cation provide marked protection against inactivation suggesting that reaction occurs in the region of the active site. The limited incorporation of DBBD into pyruvate kinase was measured by reduction of the carbonyl groups of the enzyme-bound reagent using [3H]NaBH4. When pyruvate kinase was reacted with 120 microM DBBD at pH 7.0 for 50 min in the absence of protectants, 1.8 mol of tritium/mol of subunit was incorporated, whereas in the presence of phosphoenolpyruvate with KCl, only 1.0 mol of tritium was incorporated per mole of subunit. Modified peptides were isolated from tryptic digests of pyruvate kinase. Reaction of enzyme in the presence of substrate (showing no activity loss) yielded a single peptide, Asn-Ile-X1-Lys, where X1 corresponds to Cys164 of the known amino acid sequence of muscle pyruvate kinase. In the absence of protectants, reaction for 10 min (when the enzyme retained substantial activity) yielded Asn-Ile-X1-Lys as the major labeled peptide, whereas reaction for 50 min (when the enzyme was 88% inactivated) yielded predominantly Asn-Ile-X1-Lys cross-linked to X2-Asp-Glu-Asn-Ile-Leu-Trp-Leu-Asp-Tyr-Lys, where X2 corresponds to Cys151. Because activity loss correlates with the appearance of the cross-linked peptides but not with formation of Asn-Ile-X1-Lys, inactivation is likely caused by the reaction leading to the cross-link between Cys151 and Cys164. The distance between the alpha-carbons of these residues in the crystal structure is 15.5 A, whereas only 12.0 A can be spanned by the two side chains linked by a dioxobutyl group, suggesting either that pyruvate kinase undergoes a conformational change in forming the cross-link or that local rapid fluctuations in structure occur in solution to the extent of 3.5 A in this region of pyruvate kinase.


Assuntos
Butanonas/química , Cisteína/química , Músculos/enzimologia , Fragmentos de Peptídeos/química , Piruvato Quinase/química , Sequência de Aminoácidos , Animais , Butanonas/farmacologia , Reagentes de Ligações Cruzadas , Relação Dose-Resposta a Droga , Ligantes , Modelos Químicos , Modelos Moleculares , Dados de Sequência Molecular , Fosfoenolpiruvato/farmacologia , Cloreto de Potássio/farmacologia , Piruvato Quinase/antagonistas & inibidores , Coelhos , Reagentes de Sulfidrila
11.
J Invest Dermatol ; 117(5): 1296-301, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11710947

RESUMO

In a previous study we reported that clonally expanded T cell receptor beta-chain rearrangements characterized the T cell receptor usage in skin lesions of psoriasis vulgaris and indicated antigen-specific T cell selection. To assess the relevance of clonal T cell expansion for disease progression, we now determined if select clonal T cell receptor rearrangements persisted over time and were present in nonlesional skin. Sequential biopsies were taken from psoriatic skin lesions of two patients. V-D-J junctional regions of T cell receptor beta-chain variable region gene families 2, 3, 6, 13S1, and BV17 were cloned and sequenced, as these particular BV gene families are preferentially selected in psoriatic skin lesions. The lesional T cell receptor rearrangements were compared with the T cell receptor usage in nonlesional skin and in blood. Several T cell receptor beta-chain rearrangements with high transcript frequency in the first lesional biopsy were again found in sequential lesional biopsies taken as much as 3 y later from psoriasis relapses. Only T cell receptor beta-chain rearrangements with low transcript abundance showed variability in that several clones appeared for the first time or disappeared. Although nonlesional skin also exhibited a restricted T cell receptor usage with clonal T cell receptor rearrangements, the T cell receptor usage in lesional and nonlesional skin differed nearly completely. The select lesional recurrence of identical T cell receptor rearrangements reveals that inflammation in psoriasis involves the same clonally expanded T cell populations and the same antigens over prolonged periods of time. It hereby suggests that specifically recruited and locally expanded T cell clones are permanently involved in psoriatic inflammation and may play a crucial part in disease perpetuation.


Assuntos
Rearranjo Gênico , Genes Dominantes , Psoríase/genética , Psoríase/patologia , Receptores de Antígenos de Linfócitos T alfa-beta/genética , Pele/patologia , Pele/fisiopatologia , Epitopos , Humanos , Pessoa de Meia-Idade , Psoríase/sangue , Recidiva , Linfócitos T/fisiologia
12.
J Invest Dermatol ; 115(1): 66-73, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10886510

RESUMO

Alpha beta T cells constitute an important component in the first line of immunologic defense in human skin. In order to determine the local selection forces driving T cell diversity, we studied the T cell receptor repertoire in normal human skin and compared it with that of matched blood samples. Using semiquantitative reverse transcription-polymerase chain reaction the expression of T cell receptor beta-chain V genes was determined. The majority of skin, but not blood T cells, revealed a bias towards usage of T cell receptor beta-chain V2 and V6. Whereas sequencing of T cell receptor beta-chain V2 and V6 polymerase chain reaction products showed a heterogeneous clonal distribution within these beta-chain V gene families, the analysis of other selected either over- or underrepresented beta-chain V gene families (BV3, BV12, BV13S1, BV17) revealed numerous identical T cell receptor beta-chain V transcript sequences that were not detected in blood. Restricted T cell receptor diversity in terms of beta-chain V gene preferences or clonal expansion was observed in skin samples of donors from all ages (0.5-87 y). Hence, the repertoire of T cells in normal human skin is apparently subjected to skin-specific selection throughout life. According to our data, this process could involve superantigens, which favor polyclonal accumulation of T cells using certain beta-chain V genes, as well as antigens, which induce clonal T cell expansion. Our results furthermore indicate, that T cell receptor beta-chain V repertoire restrictions do not necessarily result from disease-associated activation of the skin immune system, but could reflect regular mechanisms of immunologic homeostasis within the epithelial surface of the body.


Assuntos
Genes Codificadores dos Receptores de Linfócitos T/genética , Receptores de Antígenos de Linfócitos T alfa-beta/genética , Pele/metabolismo , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Pré-Escolar , Feminino , Perfilação da Expressão Gênica , Rearranjo Gênico da Cadeia beta dos Receptores de Antígenos dos Linfócitos T , Variação Genética , Humanos , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Transcrição Gênica
13.
Endocrinology ; 113(4): 1387-92, 1983 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-6617574

RESUMO

We examined the effects of hypophysectomy and pituitary hormone replacement on vitamin D-dependent calcium-binding protein (CaBP) in rat small intestine. The concentration of immunoreactive CaBP per mg intestinal protein was decreased by at least 56% in hypophysectomized rats compared to that in intact pair-fed controls. Alkaline phosphatase and total protein also were reduced by hypophysectomy, but pair-feeding produced comparable decreases. Daily injections of 2, 10, or 50 micrograms human GH (hGH) for 9 days produced a dose-dependent increase in CaBP. At the highest hGH dose (50 micrograms), the content of CaBP was increased 2- to 4-fold to intact levels. By comparison, the increases in total protein and alkaline phosphatase were small (25% to 40% and 80% to 90%, respectively). The induction of CaBP preceded the other protein responses; half-maximal increases in CaBP occurred after 2 days of hGH (50 micrograms/day) treatment before statistically significant changes in total protein or alkaline phosphatase activity. hGH was the most potent pituitary hormone tested; ovine TSH (25 mU/day) had no effect on CaBP, and ovine PRL (10 or 50 micrograms/day) increased CaBP by only 25-27% (P = 0.014). These studies indicate that the vitamin D-dependent intestinal CaBP in hypophysectomized rats is regulated by GH and provide further evidence that the pituitary may be involved in regulating vitamin D-dependent intestinal adaptations.


Assuntos
Proteínas de Ligação ao Cálcio/metabolismo , Hormônio do Crescimento/farmacologia , Hipofisectomia , Intestino Delgado/metabolismo , Proteína G de Ligação ao Cálcio S100/metabolismo , Fosfatase Alcalina/metabolismo , Animais , Peso Corporal/efeitos dos fármacos , Ingestão de Alimentos/efeitos dos fármacos , Feminino , Intestino Delgado/efeitos dos fármacos , Cinética , Prolactina/farmacologia , Proteínas/metabolismo , Ratos , Tireotropina/farmacologia
14.
Gene ; 46(2-3): 291-5, 1986.
Artigo em Inglês | MEDLINE | ID: mdl-2879771

RESUMO

We used an efficient sib-selection procedure to isolate a cosmid clone that complemented a mutated nit-2 gene of Neurospora crassa. Restriction fragment length polymorphism mapping indicated that the cosmid DNA insert was derived from linkage group IL, between 5S rDNA locus 12 and mt, the region of the N. crassa genome that contains nit-2. We conclude that the cosmid carries the nit-2 gene.


Assuntos
Genes Fúngicos , Genes Reguladores , Neurospora crassa/genética , Neurospora/genética , Nitrogênio/metabolismo , Mapeamento Cromossômico , Clonagem Molecular , Cosmídeos , Mutação , Neurospora crassa/metabolismo , Polimorfismo de Fragmento de Restrição
15.
Ann N Y Acad Sci ; 988: 71-9, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12796090

RESUMO

Science is concerned not just with objects but also with their various aspects, such as their colors, temperatures, sizes, and shapes. These aspects, or properties, are generally thought to be of at least two kinds: primary properties, such as shape, size, and motion and secondary ones, such as temperature and color. However, there is little agreement on just what the difference is between these two kinds of properties. An argument has recently been put forth that assumes the two kinds of properties differ only in that the secondary ones are dependent on the conditions under which they are observed. This paper suggests, however, that since the primary properties depend on conditions, too, any argument based on this assumption is flawed. There are two main traditional accounts of the distinction. The first account of the distinction-the ideas of primary qualities resemble the properties that cause these ideas, whereas those of the secondary ones do not resemble them-relies on what to many is an implausible assumption, that some of our ideas resemble features of the world and we can speak intelligibly about such resemblances. This paper suggests that we cannot, and hence we have no more reason to believe that the ideas of the primary qualities resemble aspects of the world than we do that those of the secondary qualities do so. The second traditional account-primary properties are those a body has, however small it might be, whereas secondary properties are a consequence just of relations between bodies-fares better than the other two accounts. However, the notion of force posed a serious problem for this second basis for the distinction, one that has, astonishingly, hardly found its way into the philosophical literature.

16.
Acad Med ; 64(8): 474-9, 1989 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-2751788

RESUMO

The authors evaluated human sexuality training programs at two California medical schools. In one program, students had no experience taking a sexual history. In the other, students were randomly assigned either to conduct or to observe a brief sexual history interview with a community volunteer. The students who conducted an interview showed more significant improvements in knowledge of human sexuality, perceived appropriateness of taking a sexual history and perceived personal skill in taking a sexual history than did the students who neither observed nor took a sexual history and also developed more critical views of practicing physicians' skills in taking such histories. The students who observed an interview improved more in knowledge and perceived personal skill than did the students who had no interview experience.


Assuntos
Educação de Graduação em Medicina/métodos , Anamnese , Comportamento Sexual , Humanos , Inquéritos e Questionários
17.
Biol Bull ; 199(1): 21-8, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10975639

RESUMO

Although most physiological traits scale allometrically in unitary organisms, it has been hypothesized that modularity allows for isometric scaling in colonial modular taxa. Isometry would allow increases in size without functional constraints, and is thought to be of central importance to the success of a modular design. Yet, despite its potential importance, scaling in these organisms has received little attention. To determine whether scleractinian corals are free of allometric constraints, we quantified metabolic scaling, measured as aerobic respiration, in small colonies (< or =40 mm in diam.) of the scleractinian Siderastrea siderea. We also quantified the scaling of colony surface area with biomass, since the proposed isometry is contingent upon maintaining a constant ratio of surface area to biomass (or volume) with size. Contrary to the predicted isometry, aerobic respiration scaled allometrically on biomass with a slope (b) of 0.176, and colony surface area scaled allometrically on biomass with a slope of 0.730. These findings indicate that small colonies of S. siderea have disproportionately high metabolic rates and SA:B ratios compared to their larger counterparts. The most probable explanations for the allometric scaling of aerobic respiration are (1) a decline in the SA:B ratio with size such that more surface area is available per unit of biomass for mass transfer in the smallest colonies, and (2) the small size, young age, and disproportionately high growth rates of the corals examined. This allometric scaling also demonstrates that modularity, alone, does not allow small colonies of S. siderea to overcome allometric constraints. Further studies are required to determine whether allometric scaling is characteristic of the full size range of colonies of S. siderea.


Assuntos
Cnidários/fisiologia , Animais , Cnidários/crescimento & desenvolvimento
18.
Plant Dis ; 83(11): 1058-1062, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-30841277

RESUMO

The Willamette Valley in Oregon is a major seed production area for cool-season grasses. Puccinia graminis subsp. graminicola survives over winter on its hosts as uredinial infections and causes epidemics of stem rust, the area's major disease on perennial ryegrass and tall fescue. To determine the possible importance of freezing temperature on rust survival, infected plants taken from the field were subjected to controlled freezing across a range of temperatures representative of those that can occur in the region. After treatment, plants were placed in a warm greenhouse, and the number of actively sporulating pustules was recorded at 3-day intervals for 21 days. The pathogen responded similarly to freezing treatments whether in perennial ryegrass or tall fescue. Compared with the nontreated standard, there was no significant reduction in pustule number after exposure to -3 or -6°C. Exposure of infected plants to -10°C caused a 75 to 90% reduction in rust survival, and exposure to -13°C killed all rust infections in tall fescue and over 99% in perennial ryegrass. The decline in rust survival with temperature was slightly steeper for perennial ryegrass than for tall fescue. A higher absolute number of infections in perennial ryegrass than in tall fescue resulted in higher numbers of surviving infections on perennial ryegrass. Survival of rust infections appeared to be primarily a function of host tissue survival. Between 1960 and 1997, years with winter temperatures as low as -10 or -13°C have occurred in the Willamette Valley with frequencies of approximately 39 and 8%, respectively. We conclude that year-to-year variation in winter temperature could have a significant effect on the survival of the grass stem rust pathogen.

19.
Schweiz Rundsch Med Prax ; 79(4): 64-6, 1990 Jan 23.
Artigo em Alemão | MEDLINE | ID: mdl-2406837

RESUMO

Results of sonographic investigations from 435 patients with blunt abdominal trauma or polytrauma admitted to a traumatology service are given. Complete evaluation of the abdominal organs was impeded in 94 cases by meteorism or other factors like immobility or hyperactivity of inebriated patients. Evaluation of the pancreas was inhibited in most of these cases. In 33 cases lesions of an organ could be verified during surgery. In one case the false positive diagnosis of "spleen rupture" led to operation. Suspicion of free fluid in the abdominal cavity (5 cases) could not be verified in any of the cases during a second investigation and was deemed to be negligible. Rupture of the spleen was diagnosed in 12 out of 14 cases, renal contusion in 7 out of 7 cases. Liver-, bowel- and mesenteric lesions were occasionally diagnosed indirectly (evidence for free fluid). Quality assessment did not reveal a difference between day time or nocturnal work shifts provided the investigators were experienced in sonography.


Assuntos
Traumatismos Abdominais/diagnóstico , Ultrassonografia , Ferimentos não Penetrantes/diagnóstico , Reações Falso-Positivas , Humanos , Traumatismo Múltiplo/diagnóstico , Ruptura Esplênica/diagnóstico
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