Involvement of actin filaments in mouse testicular cord organization in vivo and in vitro.

Involvement of actin filaments in mouse fetal testicular differentiation was examined in vivo and in vitro. During testicular cord formation in vivo, actin filaments accumulated in the basal cytoplasm of Sertoli cells. Addition of cytochalasin D (CD) to organ cultures of undifferentiated gonadal primordia significantly inhibited testicular cord formation. In brief, treatment with 25 ng/ml CD induced the formation of slender testicular cords, and treatment with 50 ng/ml largely inhibited cord formation in the explants. However, development and growth of the testicular parenchyma and Leydig cell differentiation occurred in the presence of CD. By electron microscopic and immunohistochemical examinations, it became clear that CD also affected formation of the basal lamina and accumulation of vimentin filaments in Sertoli cells. On the other hand, treatment with colcemid at 12.5 or 15 ng/ml prevented growth of the testicular parenchyma and development of interstitial regions. Interestingly, testicular cords formed under this condition. These results indicate that the basal actin filaments of Sertoli cells may play an important role in testicular cord formation, especially Sertoli cell polarization. Cell mitosis and/or microtubules, on the other hand, may not be directly involved in this process.     

Metaciclogénesis de Trypanosoma cruzi en Belminus ferroae (Reduviidae: Triatominae) y capacidad infectiva de las heces en condiciones de laboratorio

IntroducciónBelminus ferroae es un triatomino de comportamiento entomófago, sin embargo, puede alimentarse de vertebrados ocasionalmente. No se ha demostrado infección natural por Trypanosoma cruzi en esta especie, como tampoco la metaciclogénesis del parásito.ObjetivoExaminar la metaciclogénesis de T. cruzi en B. ferroae y la capacidad infectiva de las heces o sus contenidos intestinales en roedores.Materiales y métodosSe analizaron las heces y la orina expulsadas espontáneamente por los insectos o mediante compresión abdominal o extracción del contenido intestinal a los 10, 20, 30, 40, 50 y 60 días. Se cuantificó la carga parasitaria de T. cruzi y sus formas evolutivas se identificaron con tinción de Giemsa. Asimismo, se evaluó en ratones albinos la capacidad infectiva de los tripomastigotes metacíclicos de T. cruzi obtenidos de las heces o contenidos intestinales de los especímenes infectados.ResultadosEl análisis parasitológico reveló tres (15%) insectos infectados con T. cruzi a los 30 (n=1), 40 (n=1) y 50 (n=1) días después de la infección con cargas parasitarias de hasta 1,62 x 10⁵ tripanosomas/mm³ y porcentajes de metaciclogénesis entre el 3,5 y el 6,78%.ConclusionesSe demuestra por primera vez, en una especie del género Belminus. la metaciclogenésis de T. cruzi en condiciones de laboratorio y la capacidad infectiva de las heces para un huésped vertebrado.Palabras clave: Trypanosoma cruzi, Triatominae, enfermedad de Chagas, tripanosomiasis     

Complete nucleotide sequence of the <Emphasis Type="Italic">Cryptomeria japonica</Emphasis>D. Don. chloroplast genome and comparative chloroplast genomics: diversified genomic structure of coniferous species

Background  

The recent determination of complete chloroplast (cp) genomic sequences of various plant species has enabled numerous comparative analyses as well as advances in plant and genome evolutionary studies. In angiosperms, the complete cp genome sequences of about 70 species have been determined, whereas those of only three gymnosperm species, Cycas taitungensis, Pinus thunbergii, and Pinus koraiensis have been established. The lack of information regarding the gene content and genomic structure of gymnosperm cp genomes may severely hamper further progress of plant and cp genome evolutionary studies. To address this need, we report here the complete nucleotide sequence of the cp genome of Cryptomeria japonica, the first in the Cupressaceae sensu lato of gymnosperms, and provide a comparative analysis of their gene content and genomic structure that illustrates the unique genomic features of gymnosperms.