RESUMEN
Transposition of 1731, a Drosophila melanogaster LTR retrotransposon, was investigated in reproductive organs by RNA, protein and VLP distribution during its life cycle. We detected 1731 transcription in oogonia but not in spermatogonia; in all cells during oogenesis but only in primary spermatocytes; and in ovarian cytoplasm but both in nuclei and cytoplasm of primary spermatocytes. By confocal scanning, we showed that whereas Gag protein appeared in all cytoplasms during oogenesis, in testes Gag detection began in late premeiotic primary spermatocytes and increased in elongating spermatids suggesting distinct mechanisms of 1731 transcription and translation regulation. By electron microscopy, we did not detect 1731 VLPs in ovaries, suggesting a complex post-translational control blocking VLP assembly and transposition. Interestingly, in testes we discovered VLP aggregates in cystic cytoplasm of maturing partially individualized spermatids. In testes, we observed two delays in 1731 product expressions, suggesting a complex temporal control mechanism. Transcriptional/translational delay may be determined by accumulation of 1731 RNAs in primary spermatocyte nuclei. Translational/VLP assembly delay may be determined by post-transductional mechanisms controlling +1 frameshift and Pol-protein degradation. Our results indicated two differential mechanisms inhibiting 1731 transposition in Drosophila melanogaster ovaries and testes. In addition, we proposed a new mechanism for transposition control at the cell cycle level.
Asunto(s)
Drosophila melanogaster/virología , Retrovirus Endógenos/genética , Retroelementos , Animales , Drosophila melanogaster/ultraestructura , Retrovirus Endógenos/aislamiento & purificación , Retrovirus Endógenos/ultraestructura , Femenino , Productos del Gen env/genética , Inmunohistoquímica , Hibridación in Situ , Masculino , Ovario/ultraestructura , Secuencias Repetidas Terminales/genética , Testículo/ultraestructuraRESUMEN
Genes specifically expressed in the inner ear are candidates to underlie hereditary nonsyndromic deafness. The gene Otog has been isolated from a mouse subtractive cDNA cochlear library. It encodes otogelin, an N-glycosylated protein that is present in the acellular membranes covering the six sensory epithelial patches of the inner ear: in the cochlea (the auditory sensory organ), the tectorial membrane (TM) over the organ of Corti; and in the vestibule (the balance sensory organ), the otoconial membranes over the utricular and saccular maculae as well as the cupulae over the cristae ampullares of the three semi-circular canals. These membranes are involved in the mechanotransduction process. Their movement, which is induced by sound in the cochlea or acceleration in the vestibule, results in the deflection of the stereocilia bundle at the apex of the sensory hair cells, which in turn opens the mechanotransduction channels located at the tip of the stereo-cilia. We sought to elucidate the role of otogelin in the auditory and vestibular functions by generating mice with a targeted disruption of Otog. In Otog-/- mice, both the vestibular and the auditory functions were impaired. Histological analysis of these mutants demonstrated that in the vestibule, otogelin is required for the anchoring of the otoconial membranes and cupulae to the neuroepithelia. In the cochlea, ultrastructural analysis of the TM indicated that otogelin is involved in the organization of its fibrillar network. Otogelin is likely to have a role in the resistance of this membrane to sound stimulation. These results support OTOG as a possible candidate gene for a human nonsyndromic form of deafness.
Asunto(s)
Sordera/genética , Oído Interno/fisiopatología , Glicoproteínas de Membrana/genética , Equilibrio Postural/fisiología , Membrana Tectoria/fisiopatología , Estimulación Acústica , Animales , Mapeo Cromosómico , Cóclea/fisiología , Cóclea/fisiopatología , Sordera/patología , Sordera/fisiopatología , Oído Interno/patología , Oído Interno/fisiología , Exones , Biblioteca de Genes , Trastornos de la Audición/genética , Trastornos de la Audición/fisiopatología , Humanos , Glicoproteínas de Membrana/deficiencia , Glicoproteínas de Membrana/fisiología , Ratones , Ratones Noqueados , Postura , Reflejo/genética , Células Madre , Membrana Tectoria/patología , Membrana Tectoria/ultraestructura , TransfecciónRESUMEN
Calcium/calmodulin-dependent protein kinase II (CaM KII) is thought to be involved in the majority of the neuronal functions mediated by intracellular free Ca(2+), and has been implicated in long-term potentiation, learning, and memory. In this work, we have examined in detail the RNA expression pattern for the Drosophila CaM KII gene by in situ hybridization, during embryonic, larval, pupal, and adult stages. Our results indicate that expression of CaM KII was homogeneous in early embryos, but that during development the gene transcription rapidly became restricted to neuroblasts and their progeny in the nervous system. This predominant expression in the nervous system is maintained during late embryogenesis and post-embryonic development. A signal compartmentalization appeared in the larval central nervous system, where the CaM KII expression became progressively concentrated in the anterior ganglia. In the adult brain, a specific expression was more abundant in a subset of neurons around the central brain, particularly the mushroom bodies and the central complex, structures that play an important role in learning and memory.
Asunto(s)
Proteínas Quinasas Dependientes de Calcio-Calmodulina/genética , Drosophila melanogaster/enzimología , Drosophila melanogaster/crecimiento & desarrollo , Regulación del Desarrollo de la Expresión Génica , Genes de Insecto , Animales , Proteína Quinasa Tipo 2 Dependiente de Calcio Calmodulina , Linaje de la Célula , Sistema Nervioso Central/citología , Sistema Nervioso Central/embriología , Sistema Nervioso Central/enzimología , Sistema Nervioso Central/crecimiento & desarrollo , Drosophila melanogaster/embriología , Drosophila melanogaster/genética , Embrión no Mamífero/citología , Embrión no Mamífero/enzimología , Desarrollo Embrionario , Ganglios de Invertebrados/citología , Ganglios de Invertebrados/enzimología , Hibridación in Situ , Larva/citología , Larva/enzimología , Larva/crecimiento & desarrollo , Plasticidad Neuronal , Neuronas/citología , Neuronas/enzimología , Pupa/citología , Pupa/enzimología , Pupa/crecimiento & desarrollo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Factores de TiempoRESUMEN
Nup145p is an essential yeast nucleoporin involved in nuclear export of polyadenylated RNAs. We demonstrate here that Nup145p is cleaved in vivo to yield two functionally distinct domains: a carboxy-terminal domain (C-Nup145p) which is located at the nuclear pore complex (NPC) and assembles into the Nup84p complex, and a GLFG-containing amino-terminal domain (N-Nup145p) which is not part of this complex. Whereas the essential C-Nup145p accomplishes the functions required for efficient mRNA export and normal NPC distribution, N-Nup145p, which is homologous to the GLFG-containing nucleoporins Nup100p and Nup116p, is not necessary for cell growth. However, the N-Nup145p becomes essential in a nup188 mutant background. Strikingly, generation of a free N-domain is a prerequisite for complementation of this peculiar synthetic lethal mutant. These data suggest that N- and C-domains of Nup145p perform independent functions, and that the in vivo cleavage observed is of functional importance.
Asunto(s)
Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Membrana Nuclear/química , Proteínas de Complejo Poro Nuclear , Proteínas de Unión al ARN/química , Proteínas de Unión al ARN/metabolismo , Proteínas de Saccharomyces cerevisiae , Secuencia de Aminoácidos , Transporte Biológico/fisiología , Western Blotting , Electroforesis en Gel de Poliacrilamida , Proteínas Fúngicas/análisis , Proteínas Fúngicas/genética , Microscopía Electrónica , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida/genética , Membrana Nuclear/metabolismo , Proteínas Nucleares/metabolismo , Procesamiento Proteico-Postraduccional , ARN de Hongos/metabolismo , ARN Mensajero/metabolismo , Proteínas de Unión al ARN/análisis , Proteínas de Unión al ARN/genética , Proteínas Recombinantes de Fusión/química , Proteínas Recombinantes de Fusión/metabolismo , Homología de Secuencia de Aminoácido , Proteína Estafilocócica A/genética , Levaduras/genética , Levaduras/crecimiento & desarrollo , Levaduras/metabolismoRESUMEN
A neuroanatomical screening of a collection of P-element mutagenized flies has been carried out with the aim of finding new mutants affecting the optic lobe of the adult brain in Drosophila melanogaster. We have identified a new gene that is involved in the development of the adult axon array in the optic ganglia and in the ommatidia assembly. We have named this locus visual system disorganizer (vid). Reversional mutagenesis demonstrated that the vid mutant was the result of a P-element insertion in the Drosophila genome and allowed us to generate independent alleles, some of which resulted in semilethality, like the vid original mutant, while the others were completely lethal. A genetic somatic mosaic analysis indicated that the vid gene is required in the eye for its normal development by inductive effects. This analysis also suggests an inductive effect of the vid gene on the distal portion of the optic lobe, particularly the lamina and the first optic chiasma. Moreover, the absence of mutant phenotype in the proximal region of the optic ganglia, including the medulla, the second optic chiasma, and the lobula complex underlying mosaic eyes, is suggestive of an autonomously acting mechanism of the vid gene in the optic lobe. The complete or partial lethality generated by different mutations at the vid locus suggests that this gene's role may not be limited to the visual system, but may also affect a vital function during Drosophila development.
Asunto(s)
Drosophila melanogaster/crecimiento & desarrollo , Genes de Insecto/genética , Animales , Mapeo Cromosómico , Elementos Transponibles de ADN , Drosophila melanogaster/genética , Ojo/crecimiento & desarrollo , Genes Letales , Morfogénesis , Mosaicismo , Mutagénesis , Lóbulo Óptico de Animales no Mamíferos/crecimiento & desarrolloRESUMEN
The expression of the period (per) gene of Drosophila melanogaster has been studied by in situ hybridization in the adult's head, where it is required for the fly to exhibit behavioral circadian rhythms. We have used non-radioactive in situ hybridization to obtain a high sensitivity and specificity on head sections, with single cell resolution. Consistent with previous per protein- or per reporter gene-expression, per-expressing cells were detected in the optic lobes and the central brain, as well as in the head sensory organs: eyes, ocelli, maxillary palps and proboscis. In the brain and the eyes, circadian fluctuations of the per mRNA abundance were observed in different per expressing cells.
Asunto(s)
Ritmo Circadiano/fisiología , Drosophila melanogaster/genética , Proteínas Nucleares/genética , Animales , Proteínas de Drosophila , Drosophila melanogaster/fisiología , Cabeza , Hibridación in Situ , Proteínas Circadianas PeriodRESUMEN
Using probes specific for cAMP-dependent protein kinase, we have analyzed by in situ hybridization the patterns of expression of regulatory and catalytic subunits in mouse embryos and in adult muscle. RI alpha transcripts are distributed in muscle fibers exactly as acetylcholinesterase, showing that this RNA is localized at the neuromuscular junction. The transcript levels increase upon denervation of the muscle, but the RNA remains localized, indicating a regulation pattern similar to that of the epsilon subunit of nicotinic acetylcholine receptor. RI alpha transcripts have accumulated in the muscle by day 12 of mouse embryogenesis, and localization is established by day 14, at about the time of formation of junctions. This localization is maintained throughout development and in the adult. Immunocytochemical analysis has demonstrated that RI alpha protein is also localized. In addition, RI alpha recruits C alpha protein to the junction, providing at this site the potential for local responsiveness to cAMP. PKA could be implicated in the establishment and/or maintenance of the unique pattern of gene expression occurring at the junction, or in the modulation of synaptic activity via protein phosphorylation. Embryonic skeletal muscle shows a high level of C alpha transcripts and protein throughout the fiber; the transcripts are already present by day 12 of embryogenesis, and their elevated level is maintained only through fetal life. In the adult, the C alpha hybridization signal of muscle is weak and homogeneous.
Asunto(s)
Proteínas Quinasas Dependientes de AMP Cíclico/metabolismo , Músculo Esquelético/enzimología , Unión Neuromuscular/enzimología , Animales , Sitios de Unión , Proteínas Quinasas Dependientes de AMP Cíclico/genética , Feto/metabolismo , Regulación del Desarrollo de la Expresión Génica , Hibridación in Situ , Músculos Intercostales/embriología , Músculos Intercostales/enzimología , Ratones , Desnervación Muscular , Fibras Musculares Esqueléticas/metabolismo , Músculo Esquelético/embriología , Unión Neuromuscular/embriología , ARN/metabolismoRESUMEN
A patient infected with human immunodeficiency virus developed a diffuse cutaneous nodular syndrome. The parasite isolated from a skin nodule was studied by isoenzymatic characterization and transmission electron microscopy of both culture forms and those in the patient's skin biopsy. The parasite's ultrastructure was that of a typical member of the family Trypanosomatidae, but it differed isoenzymatically from all 'new and 'old World' species of Leishmania, Trypanosoma and Sauroleishmania. We believe that it was a (presumably) monoxenous 'lower trypanosomatid.
Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/complicaciones , Infecciones por Protozoos/complicaciones , Enfermedades Cutáneas Parasitarias/complicaciones , Trypanosomatina/ultraestructura , Infecciones Oportunistas Relacionadas con el SIDA/patología , Adulto , Animales , VIH-1 , Humanos , Masculino , Microscopía Electrónica , Infecciones por Protozoos/patología , Piel/parasitología , Piel/ultraestructura , Enfermedades Cutáneas Parasitarias/patología , Trypanosomatina/clasificaciónRESUMEN
Cystic fibrosis (CF) is characterized by a wide spectrum of clinical manifestations, including reproductive problems. Practically all males affected by the disease are infertile due to azoospermia associated with pathology of the male ducts, whereas females with CF have reduced fertility. To study the mechanism of reproductive pathology in CF patients, we analyzed the levels and localization of expression of the cystic fibrosis transmembrane regulator (CFTR) gene in relevant postnatal tissues. Significant expression was detected in the epithelium of the epididymis and vas deferens. Minimal expression, not associated with specific cell types, was seen in the mature testis. In female genitalia, variable levels of expression were seen in the cervical epithelium and fallopian tube. The endometrial epithelium and glands expressed CFTR at high levels only after puberty. No expression was seen in ovaries. Deficient secretory function of CFTR in males but not in females may lead to organ damage probably as a consequence of excessive concentration of viscid luminal contents.
Asunto(s)
Cuello del Útero/química , Fibrosis Quística , Endometrio/química , Trompas Uterinas/química , Proteínas de la Membrana/análisis , Testículo/química , Conducto Deferente/química , Adulto , Fibrosis Quística/complicaciones , Regulador de Conductancia de Transmembrana de Fibrosis Quística , Epidídimo/química , Femenino , Humanos , Hibridación in Situ , Lactante , Recién Nacido , Infertilidad/etiología , MasculinoRESUMEN
Morbidity and mortality in cystic fibrosis (CF) patients is strongly related to their respiratory disease. We have analyzed, by means of in situ hybridization, the localization and levels of CFTR mRNA in fetal, newborn, and infant respiratory tissues. Measurable levels of CFTR transcript are present in the fetal primordial epithelium of the pseudoglandular stage lung. During the following stages of lung development, CFTR expression decreases in cells of the future alveolar spaces and is gradually limited to the epithelium of the small airways. After birth, expression decreases in the small airways and is not detected in alveolar epithelia. In trachea and large bronchi, a differential pattern of expression is also observed. No CFTR expression is found in fetal submucosal glands during fetal development, but appears gradually in the newborn period. Since CFTR codes for a secretory Cl- channel, these data probably reflect the changes that occur in the lung transition from a fluid-secreting to an absorbing organ. The pattern of expression seems paradoxical in view of the clinical-pathological manifestations of CF. Although CFTR is expressed in the normal fetus and lung development is influenced by the amount of fetal lung liquid, newborns affected with CF have normal lungs. In addition, the earliest pathologic change described in CF lungs in hyperplasia of the submucosal glands, yet expression in these structures is seen only after birth. An improved understanding of the factors that alter the expected relationship between CFTR expression and pathologic lesions in the fetal lung may provide important insights into the pathogenesis and potential treatment of lung disease in CF patients.
Asunto(s)
Fibrosis Quística/metabolismo , Pulmón/metabolismo , Proteínas de la Membrana/genética , Preescolar , Fibrosis Quística/genética , Regulador de Conductancia de Transmembrana de Fibrosis Quística , ADN Complementario , Desarrollo Embrionario y Fetal/genética , Epitelio/metabolismo , Feto , Expresión Génica , Humanos , Hibridación in Situ , Lactante , Recién Nacido , Pulmón/embriología , Proteínas de la Membrana/biosíntesis , ARN Mensajero/análisis , ARN Mensajero/genética , Tráquea/metabolismoRESUMEN
Lowicryl K4M-embedded Gram-positive and Gram-negative bacteria have a tendency to separate between the cell surface and the resin. This often leads to distortion of bacteria and more especially of mycobacteria. We describe attempts made to overcome this technical problem. Different assays were made on Bacillus subtilis, Escherichia coli, and Mycobacterium avium: 1) Modification of the bacterial surface by coating of bacteria with proteinic compounds; 2) treatment of bacteria with metallic salts known to modify cell wall polysaccharides; and 3) comparison between Lowicryl K4M and HM20. Conditions have been found in which the separation of all bacterial species from the resin is abolished. The most important factor appeared to be the treatment of bacteria before dehydration, with 0.5% uranyl acetate for 30 min. The second most important factor, especially for M. avium and to a lower extent for Gram-negative bacteria, was the use of Lowicryl HM20. No differences were observed with Gram-positive bacteria between K4M and HM20. Pre-embedding in gelatin instead of agar improved sectioning of M. avium, but had no effects on the other bacterial species. These conditions applied to macrophages infected with Shigella dysenteriae or M. avium also gave excellent results. In addition to sectioning improvement of bacteria, uranyl acetate improved the ultrastructure of bacteria and macrophages. All organelles were more clearly delineated and, hence, more easily identified. Finally, it was shown that UA treatment did not affect immunogold labeling of a variety of antigens.
Asunto(s)
Resinas Acrílicas , Bacillus subtilis/ultraestructura , Escherichia coli/ultraestructura , Microscopía Electrónica/métodos , Microtomía/métodos , Mycobacterium avium/ultraestructuraRESUMEN
Expression plasmids carrying the coding sequence of mature human interleukin 1 beta (IL 1 beta) linked either to a Met start codon, or fused to different efficient Escherichia coli secretion signal sequences, have been constructed. In the latter case, we used signal peptides derived either from an outer membrane protein (OmpA) or from a periplasmic protein (PhoA). The synthesis of IL1 beta from these fusions was investigated in an otherwise strictly isogenic context using identical conditions of derepression and culture media. The Met-IL1 beta fusion produced a soluble cytoplasmic protein which could be released from the cells by osmotic shock whereas the OmpA and PhoA fusions were always insoluble. The extent of sOmpA-IL1 beta maturation was found to vary from 50 to 100%, mainly depending on the medium used, whereas no significant maturation of the signal peptide could be detected in the case of the sPhoA-IL1 beta fusion. Immuno-electron microscopy revealed that the sOmpA-IL1 beta fusion was targeted to the inner membrane, whereas the sPhoA-IL1 beta fusion remained within the cytoplasm and thus did not appear to enter the secretion pathway. Amplifying the E. coli signal peptidase lep gene on a multicopy plasmid did not improve signal peptide removal from sOmpA-IL1 beta. Moreover, these E. coli secretion vectors allowed us to produce, in high levels, IL1 beta fragments which otherwise could not be stably accumulated within the cytoplasmic compartment.
Asunto(s)
Escherichia coli/genética , Interleucina-1/genética , Señales de Clasificación de Proteína/metabolismo , Secuencia de Aminoácidos , Secuencia de Bases , Clonación Molecular , Electroforesis en Gel de Poliacrilamida , Escherichia coli/ultraestructura , Expresión Génica , Vectores Genéticos , Humanos , Interleucina-1/biosíntesis , Interleucina-1/metabolismo , Datos de Secuencia Molecular , Peso Molecular , Sondas de Oligonucleótidos , Plásmidos , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/metabolismo , Mapeo RestrictivoRESUMEN
Leishmania amastigotes are intracellular protozoan parasites which exclusively invade cells of the macrophage series and multiply within phagolysosomes. Recent studies showed that intracellular and isolated amastigotes of L. amazonesis are killed by amino acid esters which appear to be trapped within as yet unidentified, possibly acidified, "lysosome-like" parasite compartments and cleaved by hydrolytic enzyme(s) (M. Rabinovitch, V. Zilberfarb, and C. Ramazeilles, 1986, Journal of Experimental Medicine 163, 520-535). In the present study, we have localized acidic compartments of Leishmania amastigotes using as a probe the weak base 3-(2,4 dinitroanilino)-3'-amino-N-methyldipropylamine (DAMP). This indicator, which can be detected within cells by light and electron microscopy using immunocytochemical immunocytochemical methods, mainly accumulates within megasomes and in dense inclusion vacuoles. With the help of quantitative assays to titrate cell-associated DAMP, it was found that (a) its uptake is temperature dependent and thus probably requires an energy supply, (b) the proton ionophore monensin partially inhibits the trapping of DAMP, and (c) monensin greatly increases its efflux from cells. These results, as well as those obtained by quantitative ultrastructural immunocytochemistry of cells incubated with DAMP in the absence or presence of monensin, show that megasomes and inclusion vacuoles have a low pH probably maintained by an active process. Furthermore, confirming the report of H. F. Hassan and G. H. Coombs (1987, Molecular and Biochemical Parasitology 23, 285-296) megasomes were found to display acid phosphatase activity at both light and electron microscope levels. This, together with the demonstration that megasomes are acidified, suggests that these organelles may be targets for amino acid derivatives.
Asunto(s)
Leishmania/ultraestructura , Orgánulos/ultraestructura , Fosfatasa Ácida/análisis , Adamantano/análogos & derivados , Adamantano/análisis , Adamantano/metabolismo , Animales , Antagonistas del Ácido Fólico/análisis , Antagonistas del Ácido Fólico/metabolismo , Concentración de Iones de Hidrógeno , Técnicas para Inmunoenzimas , Inmunohistoquímica , Cinética , Leishmania/efectos de los fármacos , Leishmania/enzimología , Microscopía Electrónica , Monensina/farmacología , Orgánulos/enzimologíaRESUMEN
LamB is one of the major cellular proteins when E. coli is grown in the presence of maltose and is localized in the outer membrane. Previous immunolabellings obtained with monoclonal antibodies showed that this protein is a transmembrane protein and led to the detection of 4 epitopes exposed on the cell surface and 2 located on the inner surface of the outer membrane (Scheckman et al., 1983). In the present study, we have used this biological model in order to see whether these two classes of epitopes could be distinguished by immunocytochemical labelling performed on thin sections of E. coli embedded in Lowicryl K4M (Carleman et al., 1982). The optimal conditions of fixation and embedding were first established for labelling with poly- or monoclonal antibodies detected by Protein A-gold complexes. The analysis of gold particle distribution on each side of the outer membrane after labelling with a polyclonal serum or after its adsorption on intact bacteria allowed us to conclude that the resolution of immunolabelling on thin sections was about 20 nm. The use monoclonal antibodies met with difficulties due mostly to the nonspecific labelling of the cytoplasm. Although this nonospecific labelling was decreased by fixing bacteria with paraformaldehyde alone, only one antibody gave a correct specific labelling after high dilution (1/3000). The gold particle distribution obtained with this antibody confirmed the location on the cell surface of this epitope.
Asunto(s)
Proteínas Bacterianas/inmunología , Escherichia coli/inmunología , Receptores Virales/inmunología , Anticuerpos Antibacterianos/inmunología , Anticuerpos Monoclonales , Especificidad de Anticuerpos , Proteínas de la Membrana Bacteriana Externa , Bacteriófago lambda/metabolismo , Epítopos , Fijadores , Oro , PorinasRESUMEN
The nucleus of the slime mold Dictyostelium discoideum is characterized by the presence of several large dense masses which are all in tight contact with the nuclear membrane. These dense masses, considered as nucleoli, present a rather homogeneous texture, in which dense chromatin, fibrillar, and granular material are not easily detected. The autoradiographic study of [3H]uridine pulse-labeled cells showed that the majority of the silver grains were located inside these masses. The use of EDTA regressive-staining, acetylation and enzymatic digestion indicated that they are mostly composed of RNP and are totally devoid of dense chromatin as the rest of the nucleus is. After treatment with actinomycin D, fibrillar and granular material segregated but no chromatin could be found. All these observations confirmed that the dense masses correspond to nucleoli despite their peculiar ultrastructure. It can also be concluded that this type of nucleoli cannot be considered as a taxonomic character of the slime molds because it does not exist in all slime molds and was observed in some dinoflagellates, and ascomycetes.
Asunto(s)
Nucléolo Celular/ultraestructura , Dictyostelium/ultraestructura , Autorradiografía , Núcleo Celular/metabolismo , Dictyostelium/metabolismo , Ácido Edético , Microscopía Electrónica , Ribonucleoproteínas/análisis , Tritio , Uridina/metabolismoRESUMEN
The ability of concanavalin A to bind erythrocytes but not malarial parasites was used for the development of a method of merozoite isolation: cells from infected blood were allowed to bind to a column of concanavalin A linked to Sepharose beads and merozoites naturally released by maturation of the schizonts bound to the gel were collected. The principle of this method allows its application to several Plasmodium species. The kinetics of merozoite production and the quality of the preparations (purity, infectivity, and ultrastructural morphology) were investigated by using Plasmodium chabaudi.