RESUMO
Domestic cat blastocysts cultured without the zona pellucida exhibit reduced implantation capacity. However, the protein expression profile has not been evaluated in these embryos. The objective of this study was to evaluate the protein expression profile of domestic cat blastocysts cultured without the zona pellucida. Two experimental groups were generated: (1) domestic cat embryos generated by IVF and cultured in vitro (zona intact, (ZI)) and (2) domestic cat embryos cultured in vitro without the zona pellucida (zona-free (ZF group)). The cleavage, morula, and blastocyst rates were estimated at days 2, 5 and 7, respectively. Day 7 blastocysts and their culture media were subjected to liquid chromatography-tandem mass spectrometry (LC-MS/MS). The UniProt Felis catus database was used to identify the standard proteome. No significant differences were found in the cleavage, morula, or blastocyst rates between the ZI and ZF groups (p > 0.05). Proteomic analysis revealed 22 upregulated and 20 downregulated proteins in the ZF blastocysts. Furthermore, 14 proteins involved in embryo development and implantation were present exclusively in the culture medium of the ZI blastocysts. In conclusion, embryo culture without the zona pellucida did not affect in vitro development, but altered the protein expression profile and release of domestic cat blastocysts.
Assuntos
Blastocisto , Proteômica , Zona Pelúcida , Animais , Blastocisto/metabolismo , Zona Pelúcida/metabolismo , Gatos , Proteômica/métodos , Técnicas de Cultura Embrionária , Secretoma/metabolismo , Feminino , Fertilização in vitro , Proteoma/metabolismo , Desenvolvimento Embrionário , Espectrometria de Massas em Tandem , Cromatografia LíquidaRESUMO
The chorion is the primary envelop that protects the fish embryo against mechanical actions, pathogens, and abrupt changes in physical and chemicals conditions of the incubation medium. During embryo development, chorion alterations are not rare, but the occurrence of these is scarcely reported. Increased frequency of chorion alterations can result in increased embryo mortality and thus decreased reproductive performance and losses for fish farms. In this study, we characterize different chorion alterations observed in samples collected over 14 years from 12 salmon and trout farms located in the region of La Araucanía in southern Chile, which sent live eyed-stage embryos ('eyed-eggs') for quality analysis to our laboratory. We found soft chorion as the most common alteration observed, being present in the whole 14-year series analyzed in Atlantic Salmon (Salmo salar) and affecting up to 35.0% of the samples examined in a year. This alteration also affected up to 20.0 and 5.7% of Coho Salmon (Oncorhynchus kisutch) and Rainbow Trout (Oncorhynchus mykiss) samples analyzed in a year, respectively. We also found an increase of other chorion alterations, including perforated and white-spotted chorion in Atlantic and Coho Salmon, in the last 8 years. Among the three species, Rainbow Trout exhibited fewer chorion alterations. As the embryonated eggs analyzed here were obtained from broodstocks maintained under standard industrial conditions, these alterations might be linked to changes in environmental conditions affecting the incubation water that need to be further investigated.
RESUMO
This study deals with the effect of plasminogen/plasmin on the in vitro maturation (IVM) of bovine cumulus-oocyte complexes (COCs). Exogenous plasminogen activator streptokinase (SK) added to the IVM medium revealed similar values of cumulus expansion and oocyte nuclear maturation compared to controls (standard IVM medium). However, a decrease in both determinations was observed in COCs matured with the supplementation of É-aminocaproic acid (É-ACA), a specific plasmin inhibitor. After in vitro fertilization, no differences were observed in either cleavage or blastocyst rates between SK and control groups; however, ε-ACA treatment caused a decrease in both developmental rates. Zona pellucida (ZP) digestion time decreased in the SK group while it increased in the ε-ACA group. Raman microspectroscopy revealed an increase in the intensity of the band corresponding to the glycerol group of sialic acid in the ZP of oocytes matured with SK, whereas ZP spectra of oocytes treated with É-ACA presented similarities with immature oocytes. The results indicate that although treatment with SK did not alter oocyte developmental competence, it induced modifications in the ZP of oocytes that could modify the folding of glycoproteins. Plasmin inhibition impairs oocyte maturation and has an impact on embryo development, thus evidencing the importance of this protease during IVM.
Assuntos
Células do Cúmulo/metabolismo , Fibrinolisina/farmacologia , Fibrinolíticos/farmacologia , Técnicas de Maturação in Vitro de Oócitos/métodos , Oócitos/metabolismo , Oogênese/efeitos dos fármacos , Plasminogênio/farmacologia , Ácido Aminocaproico/farmacologia , Animais , Blastocisto/efeitos dos fármacos , Blastocisto/metabolismo , Bovinos , Meios de Cultura , Células do Cúmulo/efeitos dos fármacos , Técnicas de Cultura Embrionária/métodos , Desenvolvimento Embrionário/efeitos dos fármacos , Feminino , Fertilização in vitro/métodos , Fibrinolisina/antagonistas & inibidores , Oócitos/efeitos dos fármacos , Zona Pelúcida/efeitos dos fármacos , Zona Pelúcida/metabolismoRESUMO
The aims of the present study were to: (i) evaluate the ultrastructural differences in the zona pellucida (ZP) surface between immature and mature bovine oocytes, and (ii) describe a new objective technique to measure the pores in the outer ZP. Intact cumulus-oocyte complexes (COCs) obtained from a local abattoir were immediately fixed (immature group) or submitted to in vitro maturation (IVM) at 38.5 °C for 24 h in a humidified atmosphere of 5% CO2 in air (mature group). Oocytes from both groups were morphologically evaluated via Scanning Electron Microscopy (SEM) and the images were processed in the Fiji/ImageJ software using a new objective methodology through the Trainable Weka Segmentation plugin. The average number of pores in ZP was greater (p 0.05) between groups. In conclusion, it has been shown that the number of pores highlighted the main ultrastructural change in the morphology of the ZP surface of bovine oocytes during the IVM process. We have described an objective method that can be used to evaluate ultrastructural modifications of the ZP surface during oocyte maturation and early embryo development.
Assuntos
Oócitos/ultraestrutura , Zona Pelúcida/ultraestrutura , Animais , Bovinos , Processamento de Imagem Assistida por Computador , Microscopia Eletrônica de VarreduraRESUMO
The use of foetal bovine serum (FBS) in cell culture media is quite common. However, little is known about the effect of FBS on sperm. The severe difficulties in alpaca reproduction demand the search of new methods for in vitro reproductive management. In the present study, we use for the first time FBS as a supplement in the culture medium for sperm in alpaca, and the effect of FBS on motility, acrosome reaction and sperm binding to the zona pellucida in this species was evaluated. A concentration of 10% v/v FBS was used. The sperm motility with FBS at the first hour was 32.8% (vs. control = 30.0%), whereas at the second hour sperm motility with FBS was 30.2% (vs. control = 28.8%). The acrosome reaction reached an average of 44.0% for treatment with FBS (vs. control = 30.1%). The sperm-zona pellucida binding assay showed that the samples incubated with FBS had an average of 2.7 bound sperm (vs. control = 1.7). Only a significant difference was observed for sperm motility at the first hour and for the acrosome reaction. It is concluded that FBS favours the capacitation of sperm in alpaca.
Assuntos
Reação Acrossômica/efeitos dos fármacos , Camelídeos Americanos/fisiologia , Motilidade dos Espermatozoides/efeitos dos fármacos , Zona Pelúcida/efeitos dos fármacos , Animais , Bovinos , Meios de Cultura , Feminino , Sangue Fetal , Masculino , Soro , Capacitação Espermática/efeitos dos fármacos , Interações Espermatozoide-Óvulo/efeitos dos fármacos , EspermatozoidesRESUMO
BACKGROUND: In order to improve ICSI, appropiate sperm selection and oocyte activation is necessary. The objective of the present study was to determine the efficiency of fertilization using ICSI with chemically activated ovine oocytes and sperm selected by swim up (SU) or swim up + zona pellucida (SU + ZP) binding. RESULTS: Experiment 1, 4-20 replicates with total 821 in vitro matured oocytes were chemically activated with ethanol, calcium ionophore or ionomycin, to determine oocyte activation (precense of one PN). Treatments showed similar results (54, 47, 42 %, respectively) but statistically differents (P < 0.05) than mechanical activated oocytes in sham, ICSI and sham injection (13, 25, 32 %, respectively) (10-17 replicates; n = 429). Experiment 2: Twelve ejaculates and 28 straws of semen were used (11-19 replicates). Sperm were selected by SU in BSA-TCM 199-H medium. A total of 2,294 fresh sperm and 2,760 from frozen-thawed semen were analyzed after SU or SU + ZP binding. Fresh sperm selected by SU showed acrosome reaction (AR) of 59 %, the sperm selected by SU + ZP binding increased AR to 91 %. In comparison, the AR of frozen-thawed sperm using SU or SU + ZP binding was 77 and 86 %, respectively (P < 0.05). Experiment 3: fertilization in 200 mechanical activativated oocytes (17 replicates) was 4 %, but fertilization increased in ethanol activated oocytes after ICSI (12-28 %) (5-6 replicates). When fresh sperm only selected by SU were injected to 123 oocytes, a fertilization rate (28 %) was achieved; in sperm selected by SU + ZP was 25 % (73 oocytes). In comparison, in frozen-thawed sperm selected by SU, fertilization was 13 % (70 oocytes), whereas sperm from SU + ZP binding displayed 12 % (51 oocytes) (P > 0.05). CONCLUSIONS: Chemical activation induces higher ovine oocyte activation than mechanical activation. Ethanol slightly displays higher oocyte activation than calcium ionophore and ionomicine. Sperm selection with SU + ZP increased AR/A and AR/D rates in comparison with SU in fresh and frozen-thawed sperm. According to this, in terms of fertilization rates, chemical activation after ICSI increased oocyte PN formation compared to mechanical activation. Also, fresh sperm treated with SU and SU + ZP were significantly different than frozen-thawed sperm, but between sperm treatments no significant differences were obtained.
RESUMO
The mammalian oocyte is surrounded by a matrix called the zona pellucida (ZP). This envelope participates in processes such as acrosome reaction induction, sperm binding and may be involved in speciation. In cat (Felis catus), this matrix is composed of at least three glycoproteins called ZP2, ZP3, and ZP4. However, recent studies have pointed to the presence of a fourth protein in several mammals (rat, human, hamster or rabbit), meaning that a reevaluation of cat ZP is needed. For this reason, the objective of this research was to analyze the protein composition of cat ZP by means of proteomic analysis. Using ZP from ovaries and oocytes, several peptides corresponding to four proteins were detected, yielding a coverage of 33.17%, 71.50%, 50.23%, and 49.64% for ZP1, ZP2, ZP3, and ZP4, respectively. Moreover, the expression of four genes was confirmed by molecular analysis. Using total RNA isolated from cat ovaries, the complementary deoxyribonucleic acids encoding cat ZP were partially amplified by reverse-transcribed polymerase chain reaction. Furthermore, ZP1 was totally amplified for the first time in this species. As far as we are aware, this is the first study that confirms the presence of four proteins in cat ZP.
Assuntos
Gatos/genética , Proteínas do Ovo/análise , Proteínas do Ovo/genética , Expressão Gênica , Glicoproteínas de Membrana/análise , Glicoproteínas de Membrana/genética , Receptores de Superfície Celular/análise , Receptores de Superfície Celular/genética , Zona Pelúcida/metabolismo , Sequência de Aminoácidos , Animais , Proteínas do Ovo/química , Feminino , Glicoproteínas de Membrana/química , Dados de Sequência Molecular , Fases de Leitura Aberta/genética , Proteômica , RNA Mensageiro/análise , Receptores de Superfície Celular/química , Reação em Cadeia da Polimerase Via Transcriptase Reversa/veterinária , Zona Pelúcida/química , Glicoproteínas da Zona PelúcidaRESUMO
Lipid pathways play important biological roles in mammalian embryology, directing early developmental pathways to differentiation. Phospholipids and triglycerides, among others, are the main composing lipids of zona pellucida in several embryo species. Lipid analysis in embryos by mass spectrometry usually requires sample preparation and/or matrix application. This novel approach using silica plate laser desorption/ionization mass spectrometry imaging (SP-LDI-MSI) allows direct single-cell imaging and embryo region discrimination with no matrix coating. Its application is herein described for two- and eight-cell embryos. Lipid biomarkers for blastomere and intact zona pellucida are reported and corroborated by both fragmentation reactions (MS/MS) and images. Results obtained in this work are understood to be of great use for further developments on in vitro bovine fertilization. Since much of the processes can be monitored by characteristic biomarkers, it is now possible to precisely identify cell division errors during early embryo stages, as well as evaluate pre-implantation conditions.
Assuntos
Embrião de Mamíferos/metabolismo , Lipídeos/análise , Dióxido de Silício/química , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Animais , Biomarcadores/análise , Bovinos , Análise de Componente PrincipalRESUMO
Human epididymal CRISP1 (hCRISP1) associates with sperm during maturation and participates in gamete fusion through egg complementary sites. Its homology with both rodent epididymal CRISP1 and CRISP4 reported to participate in the previous stage of sperm binding to the zona pellucida (ZP), led us to further investigate the functional role of hCRISP1 by studying its involvement in human sperm-ZP interaction. Human hemizona (HZ) were inseminated with human capacitated sperm in the presence of either anti-hCRISP1 polyclonal antibody to inhibit sperm hCRISP1, or bacterially-expressed hCRISP1 (rec-hCRISP1) to block putative hCRISP1 binding sites in the ZP. Results revealed that both anti-hCRISP1 and rec-hCRISP1 produced a significant inhibition in the number of sperm bound per HZ compared with the corresponding controls. The finding that neither anti-hCRISP1 nor rec-hCRISP1 affected capacitation-associated events (i.e. sperm motility, protein tyrosine phosphorylation or acrosome reaction) supports a specific inhibition at the sperm-egg interaction level. Moreover, immunofluorescence experiments using human ZP-intact eggs revealed the presence of complementary sites for hCRISP1 in the ZP. To identify the ligand of hCRISP1 in the ZP, human recombinant proteins ZP2, ZP3 and ZP4 expressed in insect cells were co-incubated with hCRISP1 and protein-protein interaction was analyzed by ELISA. Results revealed that rec-hCRISP1 mainly interacted with ZP3 in a dose-dependent and saturable manner, supporting the specificity of this interaction. Altogether, these results indicate that hCRISP1 is a multifunctional protein involved not only in sperm-egg fusion but also in the previous stage of sperm-ZP binding through its specific interaction with human ZP3.
Assuntos
Proteínas do Ovo/genética , Glicoproteínas de Membrana/genética , Receptores de Superfície Celular/genética , Capacitação Espermática/genética , Espermatozoides/metabolismo , Zona Pelúcida/metabolismo , Reação Acrossômica/efeitos dos fármacos , Adulto , Anticorpos/farmacologia , Sítios de Ligação , Ligação Competitiva , Proteínas do Ovo/metabolismo , Proteínas do Ovo/farmacologia , Epididimo/citologia , Epididimo/efeitos dos fármacos , Epididimo/metabolismo , Feminino , Regulação da Expressão Gênica , Humanos , Masculino , Glicoproteínas de Membrana/antagonistas & inibidores , Glicoproteínas de Membrana/metabolismo , Glicoproteínas de Membrana/farmacologia , Ligação Proteica , Receptores de Superfície Celular/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Proteínas Recombinantes/farmacologia , Transdução de Sinais , Capacitação Espermática/efeitos dos fármacos , Espermatozoides/citologia , Espermatozoides/efeitos dos fármacos , Zona Pelúcida/efeitos dos fármacos , Glicoproteínas da Zona PelúcidaRESUMO
The interaction between acrosome-reacted sperm and zona pellucida proteins is not yet fully understood. Serine protease acrosin and its zymogen proacrosin have been proposed to fulfill this function due to their capacity to bind zona pellucida glycoproteins. However, the molecular mechanism underlying this interaction has been merely speculative. Here we show that fucoidan (a sulfated polysaccharide) and solubilized zona pellucida glycoproteins, but not soybean trypsin inhibitor, are able to detach bound spermatozoa, which suggests that live sperm binds to the zona pellucida in a non-enzymatical way. Interestingly, mild proteolytic digestion with acrosin or trypsin does not modify the structure of the zona pellucida, but rather results in fewer spermatozoa binding to the zona. These results agree with a model where the active site of acrosin digests the zona pellucida and binds through the polysulfate-binding domain through a three-dimensional zona structure rather than a single ligand.
Assuntos
Animais , Cricetinae , Masculino , Acrosina/metabolismo , Reação Acrossômica/fisiologia , Serina Proteases/metabolismo , Espermatozoides/enzimologia , Zona Pelúcida/metabolismo , Espermatozoides/fisiologiaRESUMO
O objetivo desta meta-análise foi avaliar o efeito da assisted hatching (AH) sobre os resultados dos ciclos de reprodução assistida: gravidez clínica, nascimento vivo, gestação múltipla, aborto e implantação embrionária, sendo avaliados os artigos publicados em periódicos indexados ao PubMed por dois autores independentes. Foram levantados 51 ensaios clínicos controlados que avaliaram o efeito da AH, sendo 40 excluídos, resultando em 11 artigos completamente avaliados. Não houve diferença significativa na taxa de gestação clínica (44,41 versus 41,30%; p=0,19, AH versus controle, respectivamente) e na taxa de nascimento vivo (36,33 versus 34,79%, p=0,63), porém, foi identificada uma tendência de aumento na taxa de gestação múltipla (18,44 versus 15,02%, p=0,05). Também não foi identificada diferença significativa na taxa de aborto (6,66 versus 6,21%, p=0,83), mas observou-se um aumento significativo na taxa de implantação embrionária (24,32 versus 21,23%, p=0,02). A partir desses resultados, pode-se concluir que, até o momento, não existe evidência suficiente para suportar o uso da AH de rotina para ciclos de reprodução assistida com transferência de embriões frescos, uma vez que não houve aumento na taxa de gravidez clínica e/ou na taxa de nascimento vivo.
The aim of this meta-analysis was to evaluate the effect of assisted hatching on the outcome of assisted reproduction cycles: clinical pregnancy, live birth, multiple pregnancy, abortion and embryonic implantation, by assessing articles published in journals indexed in PubMed by two independent authors. Fifty-one controlled trials that evaluated the effect of assisted hatching were analyzed, and 40 of them were excluded, resulting in 11 articles fully assessed. There was no significant difference in clinical pregnancy rate (44.41 versus 41.30%, p=0.19, assisted hatching versus control, respectively), and in the live birth rate (36.33 versus 34.79%, p=0.63), but we identified a trend toward increased rate of multiple pregnancies (18.44 versus 15.02%, p=0.05). We also did not identify any significant difference in the rate of abortion (6.66 versus 6.21%, p=0.83), but a significant increase in the rate of embryo implantation was observed (24.32 versus 21.23%, p=0.02). From these results, we have concluded that, until now, there is not sufficient evidence to support the use of assisted hatching for routine assisted reproduction cycles with fresh embryo transfer, since there has not been an increase in clinical pregnancy rate and/or the rate of live birth.