Increased B-lymphopoiesis by interleukin 7 induces bone loss in mice with intact ovarian function: Similarity to estrogen deficiency

Estrogen deficiency caused by ovariectomy (OVX) results in a marked bone loss due to stimulated bone resorption by osteoclasts. During our investigations of the pathogenesis of bone loss in estrogen deficiency, we found that OVX selectively stimulates B-lymphopoiesis which results in marked accumulation of B220-positive pre-B cells in mouse bone marrow. To examine the possible correlation between stimulated B-lymphopoiesis and bone loss, 8-week-old female mice were treated with interleukin (IL) 7, which stimulates B-lymphopoiesis in bone marrow. We also examined bone mass in IL-7 receptor-knockout mice that exhibit marked suppression of B-lymphopoiesis in the bone marrow. The increased B-lymphopoiesis induced by IL-7 administration resulted in marked bone loss by stimulation of osteoclastic bone resorption in mice with intact ovarian function. The changes in both B-lymphopoiesis and bone mass in IL-7-treated female mice were similar to those in age-matched OVX mice. In contrast, the trabecular bone volume of the femur was greatly increased in both female and male IL-7 receptor-knockout mice when compared with the respective wild-type and heterozygous littermates. These results show that the perturbation of B-lymphopoiesis in the bone marrow is closely linked to the change in bone mass. We propose here that the increased B-lymphopoiesis due to estrogen deficiency is involved in the mechanism of stimulated bone resorption.

Cloning and expression of rat 25-hydroxyvitamin D3-1α-hydroxylase cDNA

A full-length cDNA for the rat kidney mitochondrial cytochrome P450 mixed function oxidase, 25-hydroxyvitamin D3-1α-hydroxylase (P4501α), was cloned from a vitamin D-deficient rat kidney cDNA library and subcloned into the mammalian expression vector pcDNA 3.1(+). When P4501α cDNA was transfected into COS-7 transformed monkey kidney cells, they expressed 25-hydroxyvitamin D3-1α-hydroxylase activity. The sequence analysis showed that P4501α was of 2,469 bp long and contained an ORF encoding 501 amino acids. The deduced amino acid sequence showed a 53% similarity and 44% identity to the vitamin D3-25-hydroxylase (CYP27), whereas it has 42.6% similarity and 34% identity with the 25-hydroxyvitamin D3-24-hydroxylase (CYP24). Thus, it composes a new subfamily of the CYP27 family. Further, it is more closely related to the CYP27 than to the CYP24. The expression of P4501α mRNA was greatly increased in the kidney of vitamin D-deficient rats. In rats with the enhanced renal production of 1α,25-dihydroxyvitamin D3 (rats fed a low Ca diet), P4501α mRNA was greatly increased in the renal proximal convoluted tubules.

Ingerência humanitária : um novo paradigma em formação?

Apresentado originalmente como trabalho final do autor (especialização) -- Curso de Direito Legislativo, Universidade do Legislativo Brasileiro (Unilegis) e Universidade Federal do Mato Grosso do Sul (UFMS), 2004.

The ATPase and protease domains of yeast mitochondrial Lon: Roles in proteolysis and respiration-dependent growth

The ATP-dependent Lon protease of Saccharomyces cerevisiae mitochondria is required for selective proteolysis in the matrix, maintenance of mitochondrial DNA, and respiration-dependent growth. Lon may also possess a chaperone-like function that facilitates protein degradation and protein-complex assembly. To understand the influence of Lon’s ATPase and protease activities on these functions, we examined several Lon mutants for their ability to complement defects of Lon-deleted yeast cells. We also developed a rapid procedure for purifying yeast Lon to homogeneity to study the enzyme’s activities and oligomeric state. A point mutation in either the ATPase or the protease site strongly inhibited the corresponding activity of the pure protein but did not alter the protein’s oligomerization; when expressed at normal low levels neither of these mutant enzymes supported respiration-dependent growth of Lon-deleted cells. When the ATPase- or the protease-containing regions of Lon were expressed as separate truncated proteins, neither could support respiration-dependent growth of Lon-deleted cells; however, coexpression of these two separated regions sustained wild-type growth. These results suggest that yeast Lon contains two catalytic domains that can interact with one another even as separate proteins, and that both are essential for the different functions of Lon.

Dwarfism and early death in mice lacking C-type natriuretic peptide

Longitudinal bone growth is determined by endochondral ossification that occurs as chondrocytes in the cartilaginous growth plate undergo proliferation, hypertrophy, cell death, and osteoblastic replacement. The natriuretic peptide family consists of three structurally related endogenous ligands, atrial, brain, and C-type natriuretic peptides (ANP, BNP, and CNP), and is thought to be involved in a variety of homeostatic processes. To investigate the physiological significance of CNP in vivo, we generated mice with targeted disruption of CNP (Nppc−/− mice). The Nppc−/− mice show severe dwarfism as a result of impaired endochondral ossification. They are all viable perinatally, but less than half can survive during postnatal development. The skeletal phenotypes are histologically similar to those seen in patients with achondroplasia, the most common genetic form of human dwarfism. Targeted expression of CNP in the growth plate chondrocytes can rescue the skeletal defect of Nppc−/− mice and allow their prolonged survival. This study demonstrates that CNP acts locally as a positive regulator of endochondral ossification in vivo and suggests its pathophysiological and therapeutic implication in some forms of skeletal dysplasia.

Enhanced and accelerated lymphoproliferation in Fas-null mice.

Fas is a 45-kDa membrane protein that transduces an apoptotic signal. The mouse lymphoproliferation (lpr) mutation is a leaky mutation of Fas. In this study, we examined lymphocyte development in Fas-null mice generated by gene targeting. The Fas-/- mice progressively accumulated abnormal T cells (Thy1+, B220+, CD4-, and CD8-) and developed lymphadenopathy and splenomegaly, which were much more accelerated and pronounced than those in lpr mice. In addition, the Fas-null mice showed lymphocytosis, accompanied by lymphocytic infiltration in the lungs and liver. The number of apparently normal B cells also increased, and large amounts of immunoglobulins, including anti-DNA antibodies, were produced. Thymic clonal deletion, assessed by deletion of T cells reactive to mouse endogenous superantigens, was apparently normal in the Fas-/- mice, whereas the peripheral clonal deletion of mature T cells against a bacterial superantigen was impaired. These results suggested that Fas plays a decisive role in peripheral clonal deletion but not in negative selection in the thymus.

A possible role of vitamin D receptors in regulating vitamin D activation in the kidney.

The vitamin D endocrine system is regulated reciprocally by renal 25-hydroxyvitamin D3 1 alpha- and 24-hydroxylases. Previously, we reported that renal proximal convoluted tubules, the major site of 1 alpha, 25-dihydroxyvitamin D3 production, have vitamin D receptors. In the presence of vitamin D receptors, renal proximal convoluted tubules cannot maintain the state of enhanced production of 1 alpha, 25-dihydroxyvitamin D3. To clarify this discrepancy, we proposed a working hypothesis for the reciprocal control of renal 25-hydroxyvitamin D3 1 alpha- and 24-hydroxylase activities. In rat models of enhanced renal production of 1 alpha, 25-dihydroxyvitamin D3, expression of vitamin D receptors and 25-hydroxyvitamin D3 24-hydroxylase mRNAs was strikingly suppressed in renal proximal convoluted tubules but not in the cortical collecting ducts. In vitamin D-deficient rats with up-regulated renal 25-hydroxyvitamin D3 1 alpha-hydroxylase activity, expression of vitamin D receptor mRNA in renal proximal convoluted tubules was also down-regulated, indicating that the down-regulation of vitamin D receptor mRNA is not the result of the enhanced production of 1 alpha, 25-dihydroxyvitamin D3. In Japanese quail models with up-regulated renal 25-hydroxyvitamin D3 1 alpha-hydroxylase activity by sex steroids, expression of vitamin D receptor mRNA was also down-regulated in the kidney but not in the duodenum. These results suggest that the down-regulation of vitamin D receptors plays a critical role in production of 1 alpha, 25-dihydroxyvitamin D3 in renal proximal convoluted tubules.

The murine stk gene product, a transmembrane protein tyrosine kinase, is a receptor for macrophage-stimulating protein.

Macrophage-stimulating protein (MSP) was originally identified as an inducer of murine resident peritoneal macrophage responsiveness to chemoattractants. We recently showed that the product of RON, a protein tyrosine kinase cloned from a human keratinocyte library, is the receptor for MSP. Similarity of murine stk to RON led us to determine if the stk gene product is the murine receptor for MSP. Radiolabeled MSP could bind to NIH 3T3 cells transfected with murine stk cDNA (3T3/stk). Binding was saturable and was inhibited by unlabeled MSP but not by structurally related proteins, including hepatocyte growth factor and plasminogen. Specific binding to STK was demonstrated by cross-linking of 125I-labeled MSP to membrane proteins of 3T3/stk cells, which resulted in a protein complex with a molecular mass of 220 kDa. This radiolabeled complex comprised 125I-MSP and STK, since it could be immunoprecipitated by antibodies to the STK beta chain. Binding of MSP to stk cDNA-transfected cells induced tyrosine phosphorylation of the 150-kDa STK beta chain within 1 min and caused increased motile activity. These results establish the murine stk gene product as a specific transmembrane protein tyrosine kinase receptor for MSP. Inasmuch as the stk cDNA was cloned from a hematopoietic stem cell, our data suggest that in addition to macrophages and keratinocytes, a cell in the hematopoietic lineage may also be a target for MSP.

Estudo semântico-lexical do códice oitocentista Memoria sobre o Plano de Guerra Offensiva e Deffensiva da Capitania de Matto Grosso

Esta tese, com o intuito de contribuir para uma reflexão em torno da história da formação da língua portuguesa no Brasil, propõe como objetivo geral realizar um estudo do léxico no município de Cáceres-MT, tendo como base a discussão sobre manutenção, tendência à manutenção, desuso, tendência ao desuso e neologismo semântico de unidades lexicais extraídas de um manuscrito oitocentista. Os objetivos específicos são os seguintes: (i) compreender a história social da Capitania de Mato Grosso e do município de Cáceres, a partir das informações constantes no manuscrito Memoria, e aspectos que envolvam as condições de produção do documento e a biografia do autor; (ii) levantar o léxico do manuscrito, com recorte nos substantivos e adjetivos para servir de base na seleção das unidades lexicais a serem testadas in loco, e investigar a acepção registrada no documento das unidades lexicais, caracterizando, assim, o léxico do período oitocentista; (iii), fazer um cotejo lexicográfico abrangendo dicionários gerais dos séculos XVIII ao XXI; (iv) testar e identificar, a partir do corpus oral constituído por meio de pesquisa de campo na região urbana cacerense, o grau de manutenção, tendência à manutenção, desuso, tendência ao desuso e neologismo semântico em relação às unidades lexicais e suas respectivas acepções registradas no manuscrito. Dessa forma, toma-se como corpus de língua escrita de análise o manuscrito oitocentista Memoria sobre o plano de guerra offensiva e deffensiva da Capitania de Matto Grosso e, a partir das unidades lexicais selecionadas e extraídas dele, realizou-se a pesquisa de campo para o recolhimento do corpus de língua oral. Antes dessa recolha, tendo como base teórico-metodológica as disciplinas de Dialetologia e de Geolinguística, selecionou-se a localidade (município de Cáceres - MT) e os informantes (total de dezesseis); elaborou-se o questionário semântico-lexical, considerando fundamentalmente a proposta apresentada pelo Comitê Nacional do Projeto ALiB (2001); e realizou-se a pesquisa de campo e as transcrições das entrevistas. Para análise de natureza semântico-lexical dos corpora, recorreu aos estudos lexicográficos e lexicológicos. Tomando por base os resultados do estudo realizado, constatou-se que na realidade linguística do informante cacerense encontram-se unidades que já integravam o léxico oitocentista da língua portuguesa escrita no Brasil, ou seja, há uma memória semântico-lexical que se mantém no sistema lexical, provavelmente, devido às condições sócioculturais do município de Cáceres, Mato Grosso, cuja população, em grande parte, por quase duzentos anos, viveu na área rural. Todavia, vislumbrou-se um certo equilíbrio entre a manutenção do léxico oitocentista sem deixar de lado a inovação e o mecanismo polissêmico constitutivo do léxico.

Letter from James Winthrop to William Bentley, 1785 June 11

Two octavo-sized leaves containing a two-page handwritten letter from Winthrop to Bentley discussing the purchase of the Pentaglot Lexicon from Professor Stephen Sewall, and recent book purchases.

Letter from James Winthrop to William Bentley, 1785 December 20

Two octavo-sized leaves containing a one-page handwritten letter from Winthrop to Bentley briefly mentioning the purchase of the Pentaglot Lexicon. The second leaf is torn and a fragment, but no text is missing.

Kitāb Muqaddimat al-adab

li-Abī al-Qāsim Maḥmūd ibn ʻUmar al-Zamakhsharī.

Prof. C. Haussknecht's Routen im Orient 1865-1869: III. Kurdistan und Irak

nach dessen Originalskizzen redigirt von H. Kiepert.

Philemonis grammatici quae supersunt vulgatis et emendatiora et auctiora edidit Fridericus Osann ... Accedunt anecdota nonnulla graeca.

"Philemonis Lexicon technologicvm" (a forgery of Iakōbos Diassôrinos): p. [1]-284.

Enchiridion seu manuale hebraicum ad usum Regii Seminarii Matritensis : in duas partes distributum /

Enchiridii hebraici ... pars secunda : lexicon hebraeo-latinum.