How the site of axon emergence is specified during neural development is not understood. Previous studies disagree on the relative importance of intrinsic and extrinsic mechanisms. The axons of retinal ganglion cells (RGCs) emerge basally in vivo, yet because RGCs develop from polarized neuroepithelial cells within a polarized environment, disentangling intrinsic and extrinsic influences is a challenge. We use time-lapse imaging to demonstrate that Laminin acting directly on RGCs is necessary and sufficient to orient axon emergence in vivo. Laminin contact with the basal processes of newborn RGCs prevents the cells from entering a stochastic Stage 2 phase, directs the rapid accumulation of the early axonal marker Kif5c560-YFP, and leads to the formation of axonal growth cones. These results suggest that contact-mediated cues may be critical for the site of axon emergence and account for the differences in cellular behavior observed in vitro and in vivo.

The Oriented Emergence of Axons from Retinal Ganglion Cells Is Directed by Laminin Contact In Vivo / Randlett, Owen; Poggi, Lucia; Zolessi, Flavio R.; Harris, William A.. - In: NEURON. - ISSN 0896-6273. - 2011, 70:2(2011), pp. 266-280. [10.1016/j.neuron.2011.03.013]

The Oriented Emergence of Axons from Retinal Ganglion Cells Is Directed by Laminin Contact In Vivo

Poggi, Lucia;
2011-01-01

Abstract

How the site of axon emergence is specified during neural development is not understood. Previous studies disagree on the relative importance of intrinsic and extrinsic mechanisms. The axons of retinal ganglion cells (RGCs) emerge basally in vivo, yet because RGCs develop from polarized neuroepithelial cells within a polarized environment, disentangling intrinsic and extrinsic influences is a challenge. We use time-lapse imaging to demonstrate that Laminin acting directly on RGCs is necessary and sufficient to orient axon emergence in vivo. Laminin contact with the basal processes of newborn RGCs prevents the cells from entering a stochastic Stage 2 phase, directs the rapid accumulation of the early axonal marker Kif5c560-YFP, and leads to the formation of axonal growth cones. These results suggest that contact-mediated cues may be critical for the site of axon emergence and account for the differences in cellular behavior observed in vitro and in vivo.
2011
2
Randlett, Owen; Poggi, Lucia; Zolessi, Flavio R.; Harris, William A.
The Oriented Emergence of Axons from Retinal Ganglion Cells Is Directed by Laminin Contact In Vivo / Randlett, Owen; Poggi, Lucia; Zolessi, Flavio R.; Harris, William A.. - In: NEURON. - ISSN 0896-6273. - 2011, 70:2(2011), pp. 266-280. [10.1016/j.neuron.2011.03.013]
File in questo prodotto:
File Dimensione Formato  
Neuron_2011.pdf

accesso aperto

Tipologia: Versione editoriale (Publisher’s layout)
Licenza: Creative commons
Dimensione 3.19 MB
Formato Adobe PDF
3.19 MB Adobe PDF Visualizza/Apri

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/11572/203032
Citazioni
  • ???jsp.display-item.citation.pmc??? 60
  • Scopus 92
  • ???jsp.display-item.citation.isi??? 81
  • OpenAlex ND
social impact