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1.
Chinese Journal of Biotechnology ; (12): 2684-2694, 2023.
Article in Chinese | WPRIM | ID: wpr-981225

ABSTRACT

The aim of this study was to clone the chicken zp1 gene encoding zona pellucida 1 (Zp1) and investigate its tissues expression profile and its effect on osteoblast mineralization. The expression level of zp1 was quantified in various tissues of laying hens and in the tibia of the pre- and post-sexual maturity by RT-qPCR. Zp1 overexpressed vector was transfected into chicken calvarial osteoblasts which were induced differentiation for 8 days, and the extracellular mineral and the expression of mineralization-related genes were detected. The full-length chicken zp1 gene is 3 045 bp, encoding 958 amino acids residuals, and has two N-glycosylation sites. The highest expression level of the zp1 gene was found in the liver, followed by the tibia and yolk membrane, while no expression was detected in the heart and eggshell gland. Compared with the pre-sexual maturity hens, the concentration of estrogen (E2) in plasma, the content of glycosaminoglycan (GAG) and the expression level of the zp1 gene in the tibia with post-sexual maturity were higher. The extracellular matrix and the level of osteoblast mineralization-related genes showed a significantly upregulated expression in chicken calvarial osteoblasts with Zp1 overexpressed and addition of estrogen. The expression of the zp1 gene is tissue-specific and positively regulated osteoblast mineralization under the action of estrogen, laying the foundation for elucidating the functional properties of Zp1 in chicken bones during the egg production period.


Subject(s)
Female , Animals , Zona Pellucida Glycoproteins , Membrane Glycoproteins/metabolism , Chickens/genetics , Egg Proteins/metabolism , Receptors, Cell Surface , Estrogens
2.
Salud pública Méx ; 56(6): 654-659, nov.-dic. 2014. tab
Article in Spanish | LILACS | ID: lil-733345

ABSTRACT

La listeriosis es una enfermedad transmitida por alimentos (ETA) y ocasionada por Listeria monocytogenes. La importancia de ésta se debe a su impacto clínico, la alta tasa de mortalidad y el efecto económico derivado de los brotes asociados con el consumo de alimentos. En México, las fallas en los sistemas de vigilancia epidemiológicos son causa de información imprecisa sobre la incidencia de la listeriosis y sobre su caracterización como ETA. En este trabajo se presentan datos referentes a la presencia de la bacteria en alimentos, reportes de casos de la enfermedad y patologías relacionadas con infección por L. monocytogenes. La falta de datos exactos sobre la importancia de esta bacteria plantea la necesidad de concientizar a las instancias correspondientes para definir estrategias de búsqueda intencionada de L. monocytogenes en alimentos y de la recopilación de información clínica precisa que permita conocer la importancia clínica y epidemiológica de la listeriosis en México.


Listeriosis is caused by Listeria monocytogenes, an important food-borne disease due to its clinical forms, high mortality rate, and the economic impact in both clinical and food production industries. In Mexico, the lack of epidemiological surveillance systems leads to the need of accurate data on the incidence of listeriosis and its association with food-borne disease. In this paper, we present data about the presence of this bacterium in food, reports related to clinical cases of listeriosis, and information of diseases in which L. monocytogenes may be involved. However, in most of these cases the etiology was not established. Given this, there's a need to inform and warn the appropriate entities, to define strategies for the mandatory search of L. monocytogenes through the whole food production chain and clinical suspects, for the epidemiological importance and control of listeriosis in Mexico.


Subject(s)
Animals , Cysteine Endopeptidases/isolation & purification , Egg Proteins/metabolism , Enzyme Precursors/isolation & purification , Antimalarials/pharmacology , Chromatography, Gel , Cysteine Endopeptidases/metabolism , Cysteine Proteinase Inhibitors/pharmacology , Egg Yolk/chemistry , Electrophoresis, Polyacrylamide Gel , Enzyme Activation , Enzyme Precursors/metabolism , Hydrogen-Ion Concentration , Leucine/analogs & derivatives , Leucine/metabolism , Molecular Weight , Orthoptera
3.
Article in English | IMSEAR | ID: sea-135861

ABSTRACT

Background & objectives: An inability or decreased ability of spermatozoa to bind to the zona pellucida (ZP), an extracellular glycoproteinaceous matrix surrounding egg, is one of the plausible causes of idiopathic infertility. It will be clinically useful to distinguish this condition from other causes of infertility. An assay system, investigating binding of human sperm with ZP glycoprotein may prove useful in this regard. We attempted to develop a simple assay system to analyse the binding of capacitated human spermatozoa to human zona pellucida glycoprotein-3 (ZP3) using baculovirus-expressed recombinant human ZP3 coated beads. Methods: Recombinant baculovirus-expressed ZP3 was purified, labelled with biotin and coated on streptavidin sepharose beads. An in vitro assay system was optimized to study binding of capacitated human sperm to ZP3 coated beads. Results: A higher percentage of baculovirus-expressed recombinant human ZP3 coated beads showed significant (P<0.05) binding of capacitated human sperm as compared to beads coated with fetuin. An inhibition in the binding of sperm to ZP3 coated beads was observed in presence of cold recombinant human ZP3. Further, prior incubation of ZP3 coated beads with monoclonal antibodies (MAbs) against ZP3 but not against ZP2 resulted in the decrease in number of sperm bound to bead. Interpretation & conclusion: An in vitro assay system to study the binding of human sperm to ZP3- primary sperm receptor was established, which may be useful to determine the functional competence of spermatozoa.


Subject(s)
Egg Proteins/genetics , Egg Proteins/metabolism , Humans , Male , Membrane Glycoproteins/genetics , Membrane Glycoproteins/metabolism , Protein Binding , Receptors, Cell Surface/genetics , Receptors, Cell Surface/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Sperm Capacitation/physiology , Spermatozoa/cytology , Spermatozoa/metabolism , Zona Pellucida/metabolism , alpha-Fetoproteins/metabolism
4.
Biocell ; 26(3): 325-337, Dec. 2002.
Article in English | LILACS | ID: lil-384262

ABSTRACT

Synbranchus marmoratus (Synbranchidae), commonly known as the swamp eel, is a protogynous diandric teleost fish widely distributed throughout South America. The purpose of this work was to study the ovarian anatomy and to describe oocyte developmental stages in the swamp eel, Synbranchus marmoratus. S. marmoratus has a unique sacular ovary. It is covered by a conspicuous muscular wall, probably involved in an egg-releasing system acting as a peristaltic-like mechanism. The internal ovarian anatomy shows a U-shaped ovarian lamella delimiting a dorsal ovarian lumen. The microscopic study shows evidence of the existence of a germinal epithelium in the inner surface of the lamella, which contains germinal cells, pre-follicular cells and epithelial cells. The complete oogenesis process is divided into four stages: oogonia, primary growth, cortical alveoli and vitellogenesis. Besides, the ovulated oocytes, and atretic structures were described. The structure of the micropyle was studied by scanning electron microscopy (MEB). Near the animal pole the vitelline envelope forms crests that fuse together becoming furrow-like structures with a slightly spiraled direction that converge into the micropyle pit where is located the micropylar canal. Although the sex reversal process of Synbranchids has been subject of many studies, this is the first complete description of the ovarian anatomy and oogenesis.


Subject(s)
Female , Oogenesis , Oocytes/cytology , Ovary/anatomy & histology , Ovary/cytology , Smegmamorpha , Microscopy, Electron, Scanning , Oocytes/ultrastructure , Oogonia/cytology , Oogonia/ultrastructure , Ovary/growth & development , Egg Proteins/metabolism , Smegmamorpha/anatomy & histology , Smegmamorpha/growth & development
5.
São Paulo; s.n; 2001. 74 p. tab, graf.
Thesis in Portuguese | LILACS | ID: lil-313789

ABSTRACT

O presente experimento foi realizado no aviário da Faculdade de Medicina Veterinária e Zootecnia da Universidade Estadual Paulista do Campus de Botucatu. Foram utilizadas 288 aves da linhagem Hisex Brown, em produção, com 30 semanas de idade no início do experimento, divididas em nove tratamentos com quatro repetições cada, num esquema fatorial 3x3, sendo três níveis de energia metabolizável fornecidos por ave/dia (280, 300 e 320 kcal) e três diferentes consumos de óleo por ave/dia (0,00; 0.75 e 1,50 g). O consumo diário de ração foi restrito a 115, 110 e 105 g para obtenção dos níveis desejados de energia metabolizável e óleo. As rações foram balanceadas para que todas as aves recebessem diariamente...


Subject(s)
Animals , Chickens , Fats , Food Quality , Poultry Products/analysis , Egg Proteins/biosynthesis , Egg Proteins/metabolism , Animal Feed/analysis , Colorimetry , Eggs , Electric Power Supplies , Pedigree , Temperature , Weights and Measures
6.
Mem. Inst. Oswaldo Cruz ; 90(2): 179-184, Mar.-Apr. 1995.
Article in English | LILACS | ID: lil-319903

ABSTRACT

Incubation of total protein extracts of Schistosoma mansoni with 3H 17-beta-estradiol and 20-hydroxyecdysone, revealed steroid binding proteins in both, male and female worms. The interaction of nuclear proteins with restriction fragments of the gender and stage-specific gene F-10 was investigated using the "Band-Shift" technique. Distinct male and female nuclear proteins bound to the fragments of this gene. Among the nuclear proteins, only those rich in cysteine residues bound to DNA. In vitro incubation of live worms with the estrogen antagonist Tamoxifen, altered the pattern of the DNA binding proteins, producing in females, a band profile similar to that obtained with male worm protein extracts. When Tamoxifen was injected into schistosome infected mice, the eggs produced by females presented an abnormal morphology, compatible with non-viable eggs. These results suggest that the regulation of transcription of the F-10 gene might involve steroid receptors.


Subject(s)
Animals , Male , Female , Cricetinae , DNA-Binding Proteins , Helminth Proteins/metabolism , Egg Proteins/metabolism , Schistosoma mansoni , Sex Characteristics , Genes, Helminth , Protein Binding , Nuclear Proteins/metabolism , Schistosoma mansoni
7.
Arch. latinoam. nutr ; 36(4): 701-13, dic. 1986. ilus, tab
Article in English | LILACS | ID: lil-103760

ABSTRACT

La utilización biológica de la proteína dietaria, el más costoso de los nutrientes requeridos por el organismo, sigue siendo un tópico de importancia, particularmente para los países del Tercer Mundo, donde los abastecimientos proteínicos frecuentemente son limitados. Como medio de incrementar la ingesta de proteína, a menudo se utiliza la suplementación con proteína de cereales y otros productos alimenticios. Esa suplementación no solo aumenta la ingesta de dicho nutriente, sino que a menudo tambien induce cambios en la utilización fisiológica del componente proteínico de la mezcla resultante. El autor investigó la naturaleza de esos cambios en cuanto a la asimilabilidad de la proteína, como resultado de cambios escalonados en las proporciones de ciertas proteínas que, en combinaciones por pareja, se incorporan a mexclas simples. Empleó para el caso un método biológico actualizado de evaluación del valor nutricional de la proteína. Se presentan datos con base en los caules es factible estimar la digestibilidad y/o asimilabilidad del componente protéinico de una mezcla dada. Por último, el autor señala la necesidad de evaluar alimentos ricos en proteína y suplementos proteínicos, no sólo en términos de su contenido de proteína en relación al costo, si no también del valaor nutritivo inherente, y de su efecto complementario


Subject(s)
Animals , Rats , Egg Proteins/metabolism , Food, Formulated , Food, Fortified , Lysine/metabolism , Milk Proteins/metabolism , Plant Proteins/metabolism , Biological Availability , Energy Intake , Glutens/metabolism , Nutritive Value , Solanum tuberosum , Zea mays
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