Cerebellar GABAergic interneurons in mouse comprise multiple subsets of morphologically and neurochemically distinct phenotypes located at strategic nodes of cerebellar local circuits. These cells are produced by common progenitors deriving from the ventricular epithelium during embryogenesis and from the prospective white matter (PWM) during postnatal development. However, it is not clear whether these progenitors are also shared by other cerebellar lineages and whether germinative sites different from the PWM originate inhibitory interneurons. Indeed, the postnatal cerebellum hosts another germinal site along the Purkinje cell layer (PCL), in which Bergmann glia are generated up to first the postnatal weeks, which was proposed to be neurogenic. Both PCL and PWM comprise precursors displaying traits of juvenile astroglia and neural stem cell markers. First, we examine the proliferative and fate potential of these niches, showing that different proliferative dynamics regulate progenitor amplification at these sites. In addition, PCL and PWM differ in the generated progeny. GABAergic interneurons are produced exclusively by PWM astroglial-like progenitors, whereas PCL precursors produce only astrocytes. Finally, through in vitro, ex vivo, and in vivo clonal analyses we provide evidence that the postnatal PWM hosts a bipotent progenitor that gives rise to both interneurons and white matter astrocytes

Heterogeneity and bipotency of astroglial-like cerebellar progenitors along the interneuron and glial lineages

PARMIGIANI, ELENA;LETO, Ketty;BUFFO, Annalisa
;
ROSSI, Ferdinando
2015-01-01

Abstract

Cerebellar GABAergic interneurons in mouse comprise multiple subsets of morphologically and neurochemically distinct phenotypes located at strategic nodes of cerebellar local circuits. These cells are produced by common progenitors deriving from the ventricular epithelium during embryogenesis and from the prospective white matter (PWM) during postnatal development. However, it is not clear whether these progenitors are also shared by other cerebellar lineages and whether germinative sites different from the PWM originate inhibitory interneurons. Indeed, the postnatal cerebellum hosts another germinal site along the Purkinje cell layer (PCL), in which Bergmann glia are generated up to first the postnatal weeks, which was proposed to be neurogenic. Both PCL and PWM comprise precursors displaying traits of juvenile astroglia and neural stem cell markers. First, we examine the proliferative and fate potential of these niches, showing that different proliferative dynamics regulate progenitor amplification at these sites. In addition, PCL and PWM differ in the generated progeny. GABAergic interneurons are produced exclusively by PWM astroglial-like progenitors, whereas PCL precursors produce only astrocytes. Finally, through in vitro, ex vivo, and in vivo clonal analyses we provide evidence that the postnatal PWM hosts a bipotent progenitor that gives rise to both interneurons and white matter astrocytes
2015
35
19
7388
7402
http://www.jneurosci.org/content/35/19/7388.full.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705428/
Bergmann glia; Cerebellum; Mouse brain; Multipotent progenitors; Neurogenesis; Prospective white matter; Actins; Animals; Animals, Newborn; Antigens, CD2; Cell Differentiation; Cell Proliferation; Cells, Cultured; Cerebellum; Embryo, Mammalian; Estrogen Antagonists; Excitatory Amino Acid Transporter 1; Female; GABAergic Neurons; Gene Expression Regulation, Developmental; Interneurons; Lymphocytic Choriomeningitis; Lymphocytic choriomeningitis virus; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neuroglia; Stem Cells; Tamoxifen; White Matter; Neuroscience (all); Medicine (all)
Parmigiani, Elena; Leto, Ketty; Rolando, Chiara; Figueres-Oñate, María; López-Mascaraque, Laura; Buffo, Annalisa; Rossi, Ferdinando
File in questo prodotto:
File Dimensione Formato  
7388.ok.pdf

Accesso riservato

Tipo di file: PDF EDITORIALE
Dimensione 8.27 MB
Formato Adobe PDF
8.27 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1532162
Citazioni
  • ???jsp.display-item.citation.pmc??? 28
  • Scopus 50
  • ???jsp.display-item.citation.isi??? 44
social impact