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Glomeruli are cell-free neuropil structures that emerge during prenatal and postnatal development. Within glomeruli, the axons of olfactory sensory neurons form glutamatergic synapses with the dendrites of mitral and tufted cells, the second-order neurons in the olfactory pathway. The neuroanatomist Camillo Golgi, using his newly developed silver impregnation technique, was the first to report olfactory bulb glomeruli, in the year 1875. Santiago Ramón y Cajal described in 1890 their shape as “de forma de pera ó bota de vino”. Apparently, glomeruli represented an anatomical unit and, most likely, a functional unit as well. However, their definitive characteristic and the key determinant responsible for the formation of glomeruli during development remained elusive for more than a century. The precise nature of the glomerulus as a unit was elucidated through molecular and genetic studies in the wake of the discovery of odorant receptor genes in 1991. We have developed a genetic technique, based on an internal ribosome entry site and an axonal marker, to specifically label individual olfactory sensory neurons that express one of the 1141 inact odorant receptor genes in mouse. Our technique enables the direct observation, on whole mounts or in histological sections, of the coalescence of axons of olfactory sensory neurons expressing the same odorant receptor gene into two (sometimes three) glomeruli per olfactory bulb – one located in the medial half and the other in the lateral half. The exact number of glomeruli per olfactory bulb has remained unclear, a century and a half after their discovery. Recently we have devised a methodology for quantifying the number, size, and shape of the glomeruli, by imaging olfactory bulbs labeled immunohistochemically as whole mounts with serial two-photon tomography. We counted a median of 2851 glomeruli per olfactory bulb at postnatal day 56, corresponding to 2.50 glomeruli per intact odorant receptor gene per olfactory bulb. By quantifying glomerular shape with aspect-length ratios and sphericity, we demonstrate that glomeruli do not conform to spherical shapes. We propose the descriptor “tuberiform” to encompass the diversity of glomerular shapes.
Información relacionada: https://onlinelibrary.wiley.com/doi/10.1111/ejn.70327?af=R
La Sección Biología Celular (SBC) desarrolla actividades de enseñanza para estudiantes de las Licenciaturas de Biología, Bioquímica y Biología Humana.
De acuerdo a los Planes de Estudio actuales, realiza el curso “Biología Celular”, curso del Ciclo Básico, que tiene lugar en el primer semestre del año. Para el Ciclo de Profundización y para Maestrías realiza el curso “Biología del Desarrollo”, emplazado en el segundo semestre del año. Además, docentes de la Sección coordinan y dictan clases en el modulo “La Célula” del curso de Introducción a la Biología/Biología General.
También como actividades de Pre-grado, en sus laboratorios se realizan Pasantías curriculares de trabajo experimental. Para Post-grado se organizan cursos especializados para las Maestrías en Biología Celular y Molecular del PEDECIBA y se orientan Tesis de Maestría y de Doctorado.
En la SBC existen varios grupos de investigación y el “Laboratorio de Cultivo de Tejidos” (antiguo laboratorio fundado en la Facultad de Medicina muchas décadas atrás).
Algunas publicaciones recientes de integrantes de la Sección Biología Celular:
Sharkova M, Aparicio G, Mouzaaber C, Zolessi FR, Hocking JC (2024) Photoreceptor calyceal processes accompany the developing outer segment, adopting a stable length despite a dynamic core. J Cell Sci 13:jcs.261721. https://doi.org/10.1242/jcs.261721
Montagne J, Preza M, Koziol U (2023). Stem cell proliferation and differentiation during larval metamorphosis of the model tapeworm Hymenolepis microstoma. Front Cell Infect Microbiol. 13:1286190. doi: 10.3389/fcimb.2023.1286190
Calvelo J, Brehm K, Iriarte A, Koziol U (2023) Trans-splicing in the cestode Hymenolepis microstoma is constitutive across the life cycle and depends on gene structure and composition. Int J Parasitol. 2023 Feb;53(2):103-117. doi: 10.1016/j.ijpara.2022.11.006
Preza M, Van Bael S, Temmerman L, Guarnaschelli I, Castillo E, Koziol U (2022) Global analysis of neuropeptides in cestodes identifies Attachin, a SIFamide homolog, as a stimulant of parasite motility and attachment. J. Neurochem. 162(6):467-482. doi: 10.1111/jnc.15654
Davison C, Bedó G, Zolessi FR (2022) Zebrafish Slit2 and Slit3 act together to regulate retinal axon crossing at the midline. J. Dev. Biol. 10(4), 41. doi: 10.3390/jdb10040041 Preprint: bioRxiv https://doi.org/10.1101/2022.08.12.503757
Eastman G, Sharlow ER, Lazo JS, Bloom GS, Sotelo-Silveira JR (2022) Transcriptome and Translatome Regulation of Pathogenesis in Alzheimer's Disease Model Mice. J Alzheimers Dis 86(1):365-386. doi: 10.3233/JAD-215357
Oliveira-Rizzo C, Ottati MC, Fort RS, Chavez S, Trinidad JM, DiPaolo A, Garat B, Sotelo-Silveira JR, Duhagon MA (2022) Hsa-miR-183-5p Modulates Cell Adhesion by Repression of ITGB1 Expression in Prostate Cancer. Noncoding RNA 8(1):11. doi: 10.3390/ncrna8010011
Veloz L, Bosch SA, Aparicio G, Zolessi FR (2022) Cell extrusion in development and cancer, what MARCKS the difference for epithelial integrity? BIOCELL 46(3) 639-644. doi: 10.32604/biocell.2022.018798.
Chalar C, Clivio G, Montagne J, Costábile A, Lima A, Papa NG, Berois N, Arezo MJ (2021) Embryonic developmental arrest in the annual killifish Austrolebias charrua: A proteomic approach to diapause III. PLoS One 16(6):e0251820. doi: 10.1371/journal.pone.0251820
Zolessi FR, Berois N, Brauer MM, Castillo E (2021) Building the embryo of developmental biology in Uruguay. Intl J Devl Biol 65: 71 - 76. doi: 10.1387/ijdb.200141fz