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  1. AU="Posada-Pérez, Mercedes"
  2. AU=Metlay Joshua P
  3. AU="Maxime Mermod"
  4. AU="Asrani, R K"
  5. AU=Cook Daniel C
  6. AU=Clark T G
  7. AU="Batina, Nikola"
  8. AU="Busche, Jacob A"
  9. AU="Quaresima, Luigi"
  10. AU="Arnaud Gautier"
  11. AU="Leary Peter"
  12. AU="Currò, Mariaconcetta"
  13. AU=Schulte Ryan T
  14. AU=Wichmann D
  15. AU="Arora, Prateek"
  16. AU="Junqueira, Helena Couto"
  17. AU="Kataria, Saurabh"
  18. AU=Wang Xia AU=Wang Xia
  19. AU="Tonnesen, Morten"
  20. AU="Ebrahimi-Fakhari, Darius"
  21. AU="Kalinich, Chaney C"
  22. AU="O'Neal, David N"
  23. AU="Bennett, Matthew R"
  24. AU="Chagas, Mariana W"

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  1. Artikel ; Online: Microglial Caspase-3 is essential for modulating hippocampal neurogenesis.

    Alonso Bellido, Isabel M / Posada-Pérez, Mercedes / Hernández-Rasco, Francisco / Vázquez-Reyes, Sandra / Cabanillas, María / Herrera, Antonio J / Bachiller, Sara / Soldán-Hidalgo, Jesús / Espinosa-Oliva, Ana M / Joseph, Bertrand / de Pablos, Rocío M / Venero, José L / Ruiz, Rocío

    Brain, behavior, and immunity

    2023  Band 112, Seite(n) 206–219

    Abstract: Adult hippocampal neurogenesis (AHN) is a process involved in numerous neurodegenerative diseases. Many researchers have described microglia as a key component in regulating the formation and migration of new neurons along the rostral migratory stream. ... ...

    Abstract Adult hippocampal neurogenesis (AHN) is a process involved in numerous neurodegenerative diseases. Many researchers have described microglia as a key component in regulating the formation and migration of new neurons along the rostral migratory stream. Caspase-3 is a cysteine-aspartate-protease classically considered as one of the main effector caspases in the cell death program process. In addition to this classical function, we have identified the role of this protein as a modulator of microglial function; however, its action on neurogenic processes is unknown. The aim of the present study is to identify the role of Caspase-3 in neurogenesis-related microglial functions. To address this study, Caspase-3 conditional knockout mice in the microglia cell line were used. Using this tool, we wanted to elucidate the role of this protein in microglial function in the hippocampus, the main region in which adult neurogenesis takes place. After the reduction of Caspase-3 in microglia, mutant mice showed a reduction of microglia in the hippocampus, especially in the dentate gyrus region, a region inherently associated to neurogenesis. In addition, we found a reduction in doublecortin-positive neurons in conditional Caspase-3 knockout mice, which corresponds to a reduction in neurogenic neurons. Furthermore, using high-resolution image analysis, we also observed a reduction in the phagocytic capacity of microglia lacking Caspase-3. Behavioral analysis using object recognition and Y-maze tests showed altered memory and learning in the absence of Caspase-3. Finally, we identified specific microglia located specifically in neurogenic niche positive for Galectin 3 which colocalized with Cleaved-Caspase-3 in control mice. Taken together, these results showed the essential role of Caspase-3 in microglial function and highlight the relevant role of this specific microglial phenotype in the maintenance of AHN in the hippocampus.
    Mesh-Begriff(e) Animals ; Mice ; Caspase 3/metabolism ; Hippocampus/metabolism ; Mice, Knockout ; Microglia/metabolism ; Neurogenesis/physiology
    Chemische Substanzen Caspase 3 (EC 3.4.22.-)
    Sprache Englisch
    Erscheinungsdatum 2023-06-15
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639219-2
    ISSN 1090-2139 ; 0889-1591
    ISSN (online) 1090-2139
    ISSN 0889-1591
    DOI 10.1016/j.bbi.2023.06.013
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: ARG1-expressing microglia show a distinct molecular signature and modulate postnatal development and function of the mouse brain.

    Stratoulias, Vassilis / Ruiz, Rocío / Kanatani, Shigeaki / Osman, Ahmed M / Keane, Lily / Armengol, Jose A / Rodríguez-Moreno, Antonio / Murgoci, Adriana-Natalia / García-Domínguez, Irene / Alonso-Bellido, Isabel / González Ibáñez, Fernando / Picard, Katherine / Vázquez-Cabrera, Guillermo / Posada-Pérez, Mercedes / Vernoux, Nathalie / Tejera, Dario / Grabert, Kathleen / Cheray, Mathilde / González-Rodríguez, Patricia /
    Pérez-Villegas, Eva M / Martínez-Gallego, Irene / Lastra-Romero, Alejandro / Brodin, David / Avila-Cariño, Javier / Cao, Yang / Airavaara, Mikko / Uhlén, Per / Heneka, Michael T / Tremblay, Marie-Ève / Blomgren, Klas / Venero, Jose L / Joseph, Bertrand

    Nature neuroscience

    2023  Band 26, Heft 6, Seite(n) 1008–1020

    Abstract: Molecular diversity of microglia, the resident immune cells in the CNS, is reported. Whether microglial subsets characterized by the expression of specific proteins constitute subtypes with distinct functions has not been fully elucidated. Here we ... ...

    Abstract Molecular diversity of microglia, the resident immune cells in the CNS, is reported. Whether microglial subsets characterized by the expression of specific proteins constitute subtypes with distinct functions has not been fully elucidated. Here we describe a microglial subtype expressing the enzyme arginase-1 (ARG1; that is, ARG1
    Mesh-Begriff(e) Animals ; Female ; Mice ; Arginase/genetics ; Arginase/metabolism ; Hippocampus/metabolism ; Microglia/metabolism
    Chemische Substanzen Arginase (EC 3.5.3.1) ; Arg1 protein, mouse (EC 3.5.3.1)
    Sprache Englisch
    Erscheinungsdatum 2023-05-11
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1420596-8
    ISSN 1546-1726 ; 1097-6256
    ISSN (online) 1546-1726
    ISSN 1097-6256
    DOI 10.1038/s41593-023-01326-3
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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