TiS21 knock-out enhances the frequency of medulloblastoma in Patched1 heterozygous mice by inhibiting the Cxcl3-dependent migration of cerebellar neurons

Stefano Farioli-Vecchioli, Irene Cinà, Manuela Ceccarelli, Laura Micheli, Luca Leonardi, Maria Teresa Ciotti, Marco De Bardi, Concezio Di Rocco, Roberto Pallini, Sebastiano Cavallaro, Felice Tirone

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Abstract

A failure in the control of proliferation of cerebellar granule neuron precursor cells (GCPs), located in the external granular layer (EGL) of the cerebellum, gives rise to medulloblastoma. To investigate the process of neoplastic transformation of GCPs, we generated a new medulloblastoma model by crossing Patched1 heterozygous mice, which develop medulloblastomas with low frequency, with mice lacking the Tis21 gene. Overexpression of Tis21 is known to inhibit proliferation and trigger differentiation of GCPs; its expression decreases in human medulloblastomas. Double-knock-out mice show a striking increase in the frequency of medulloblastomas and hyperplastic EGL lesions, formed by preneoplastic GCPs. Tis21 deletion does not affect the proliferation of GCPs but inhibits their differentiation and, chiefly, their intrinsic ability to migrate outside the EGL. This defect of migration may represent an important step in medulloblastoma formation, as GCPs, remaining longer in the EGL proliferative niche, may become more prone to transformation. By genome-wide analysis, we identified the chemokine Cxcl3 as a target of Tis21. Cxcl3 is downregulated in Tis21-null GCPs of EGL and lesions; addition of Cxcl3 to cerebellar slices rescues the defective migration of Tis21-null GCPs and, remarkably, reduces the area of hyperplastic lesions. As Tis21 activates Cxcl3 transcription, our results suggest that Tis21 induces migration of GCPs through Cxcl3, which may represent a novel target for medulloblastoma therapy.

Original languageEnglish
Pages (from-to)15547-15564
Number of pages18
JournalJournal of Neuroscience
Volume32
Issue number44
DOIs
Publication statusPublished - Oct 31 2012

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Medulloblastoma
Neocortex
Neurons
Neoplastic Processes
Chemokines
Knockout Mice
Cerebellum
Down-Regulation
Genome
Genes

ASJC Scopus subject areas

  • Neuroscience(all)

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TiS21 knock-out enhances the frequency of medulloblastoma in Patched1 heterozygous mice by inhibiting the Cxcl3-dependent migration of cerebellar neurons. / Farioli-Vecchioli, Stefano; Cinà, Irene; Ceccarelli, Manuela; Micheli, Laura; Leonardi, Luca; Ciotti, Maria Teresa; De Bardi, Marco; Di Rocco, Concezio; Pallini, Roberto; Cavallaro, Sebastiano; Tirone, Felice.

In: Journal of Neuroscience, Vol. 32, No. 44, 31.10.2012, p. 15547-15564.

Research output: Contribution to journalArticle

Farioli-Vecchioli, S, Cinà, I, Ceccarelli, M, Micheli, L, Leonardi, L, Ciotti, MT, De Bardi, M, Di Rocco, C, Pallini, R, Cavallaro, S & Tirone, F 2012, 'TiS21 knock-out enhances the frequency of medulloblastoma in Patched1 heterozygous mice by inhibiting the Cxcl3-dependent migration of cerebellar neurons', Journal of Neuroscience, vol. 32, no. 44, pp. 15547-15564. https://doi.org/10.1523/JNEUROSCI.0412-12.2012
Farioli-Vecchioli, Stefano ; Cinà, Irene ; Ceccarelli, Manuela ; Micheli, Laura ; Leonardi, Luca ; Ciotti, Maria Teresa ; De Bardi, Marco ; Di Rocco, Concezio ; Pallini, Roberto ; Cavallaro, Sebastiano ; Tirone, Felice. / TiS21 knock-out enhances the frequency of medulloblastoma in Patched1 heterozygous mice by inhibiting the Cxcl3-dependent migration of cerebellar neurons. In: Journal of Neuroscience. 2012 ; Vol. 32, No. 44. pp. 15547-15564.
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AU - Micheli, Laura

AU - Leonardi, Luca

AU - Ciotti, Maria Teresa

AU - De Bardi, Marco

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