The Union between gracilis and sartorius muscles in leontopithecus: morphofunctional analysis

RESUMEN: El Tití León Dorado, (Leontopithecus rosalia) es un primate (especie de los Tamarinos y Titíes) de la foresta atlántica brasileña en serio riesgo de extinción. Poco se conoce acerca de su anatomía, específicamente de las uniones musculares. Debido a ello, con el objetivo de comprender la locomoción de éste y otros primates, estudiamos la morfología y morfometría de los músculos grácil y sartorio y la relación entre ellos, en 3 especies de Leontopithecus rosalia. Se examinaron 18 animales adultos, de ambos sexos, sin anormalidades físicas en la región estudiada. El material pertenece a la colección del Centro de Primatología de Rio de Janeiro, Brasil. Los miembros posteriores fueron disecados hasta el nivel de los músculos grácil y sartorio, donde se efectuó la morfometría, obteniéndose, entre los músculos mencionados un área para su análisis histológico. Describimos la morfología de los músculos grácil y sartorio. Se obtuvieron valores promedio de la morfometría muscular y se estudió histológicamente la unión entre esos músculos. El análisis morfológico y morfométrico permite sugerir parámetros descriptivos de esos músculos. El análisis histológico permite concluir que las fibras del músculo grácil y del músculo sartorio no están fusionadas sino que se mantienen juntas a través de tejido conjuntivo, así, se insertan en el lado medial de la tibia. Funcionalmente, creemos que los músculos grácil y sartorio contribuyen a una activa contención de la articulación de la rodilla y sobre la biomecánica de los miembros posteriores de esos primates, conocidos como corredores.

Cytochemical study of Streptococcus agalactiae and macrophage interaction.

Light and electron microscopy were used to analyse the process of interaction of Streptococcus agalactiae (serotypes Ia, III, and V) with resident and activated mouse peritoneal macrophages. Transmission electron microscopy showed that adherence of the S. agalactiae serotype Ia, but not III and V serotypes, to the surface of activated macrophages triggers the respiratory oxidative burst as revealed by the presence of reduced nicotinamide adenine dinucleotide (phosphate) [NAD(P)H]-oxidase in the phagocytic vacuoles. Fusion of macrophage lysosomes with bacteria-containing phagocytic vacuoles was observed in macrophages treated with Lucifer yellow as well as by localization of acid phosphatase for all serotypes.

An ultrastructural and cytochemical study of Tritrichomonas foetus-eosinophil interaction.

The fine structure of the process of interaction between uncoated and antibody-coated Tritrichomonas foetus with rat peritoneal eosinophils was studied. Eosinophils were purified by discontinuous Metrizamide gradient. Agglutination and immunofluorescence microscopy showed that T.foetus grown in a medium supplemented with different kinds of serum, antibodies present in it opsonize the parasites. Parasites incubated in the presence of anti-T.foetus rabbit serum attach to and are ingested by eosinophils. No such attachment was observed with trypsin-treated parasites. Attachment of antibody-coated parasites to the eosinophils induced their degranulation with the release of granule contents onto parasite surface causing its destruction. Hyperimmune serum was shown to be required for both attachment and ingestion of the parasites. The cytochemical localization of basic proteins and peroxidase showed that leucocyte granules fused with parasite-containing phagocytic vacuoles. Images were obtained suggesting that the binding of the parasites to the eosinophil surface triggers an exocytic process with release of the granule content onto the parasite surface.

Fine structure and cytochemistry of Tritrichomonas foetus and rat neutrophil interaction.

The fine structure of normal and antibody-coated Tritrichomonas foetus cells and their interaction with rat peritoneal neutrophils was studied. Peritoneal neutrophils were obtained by glycogen stimulation. The neutrophils readily associated with and killed the parasites, which were subsequently ingested. The process involved activation of the respiratory burst, as demonstrated by the use of cytochemical methods. Images were obtained indicating that binding of parasites to the neutrophil surface triggers an exocytic response with release of oxygen-derived products. Cytochemical localization of acid phosphatase and peroxidase activities showed that leukocyte granules fused with the parasite-containing phagocytic vacuoles. We also showed the cytochemical localization of alkaline phosphatase in the parasite-neutrophil interaction.

A cytochemical study of the interaction between Tritrichomonas foetus and mouse macrophages.

Light and electron microscopy were used to analyse the process of interaction of normal and antibody-coated Tritrichomonas foetus with resident and activated mouse peritoneal macrophages. Activated macrophages ingest more parasites than do resident macrophages. Previous incubation of the parasites in the presence of sub-agglutinating concentrations of a polyclonal anti-T. foetus antibody significantly increased their ingestion by the macrophages. Adherence of the parasites to the surface of activated macrophages triggers the respiratory oxidative burst as revealed by reduction of nitroblue tetrazolium. This process was more evident in antibody-coated parasites. Transmission electron microscopy showed the presence of reduced nicotinamide adenine dinucleotide (phosphate) [NAD(P)H]-oxidase in the portions of the macrophage plasma membrane that were in contact with the parasites as well as in the phagocytic vacuoles. Fusion of macrophage lysosomes with parasite-containing phagocytic vacuoles was observed in macrophages labeled with Lucifer yellow and gold-labeled peroxidase as well as by localisation of acid phosphatase.

The interaction of Tritrichomonas foetus and Trichomonas vaginalis with macrophages.

The process of interaction between macrophages and Tritrichomonas foetus and Trichomonas vaginalis was analysed using light microscopy, scanning and transmission electron microscopy. The parasites attach to the macrophage surface and are ingested through a phagocytic process. Parasite-macrophage association index was higher for activated than for resident macrophages. Previous incubation of the parasites in the presence of Concanavalin A rendered their surface less negative and more hydrophobic, as evaluated by measurement of the zeta potential and contact angle, respectively. This treatment significantly increased parasite ingestion by resident, but not activated macrophages.