Differentiated horizontal Interneurons clonally expand to form metastatic retinoblastoma in mice

被引:159
作者
Ajioka, Itsuki
Martins, Rodrigo A. P.
Bayazitov, Ildar T.
Donovan, Stacy
Johnson, Dianna A.
Frase, Sharon
Cicero, Samantha A.
Boyd, Kelli
Zakharenko, Stanislav S.
Dyer, Michael A.
机构
[1] St Jude Childrens Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[2] Univ Tennessee, Coll Med, Hlth Sci Ctr, Dept Ophthalmol, Memphis, TN 38105 USA
[3] Univ Memphis, Integrated Microscopy Ctr, Memphis, TN 38152 USA
[4] St Jude Childrens Hosp, Anim Resources Ctr, Div Pathol, Memphis, TN 38105 USA
关键词
D O I
10.1016/j.cell.2007.09.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During neurogenesis, the progression from a progenitor cell to a differentiated neuron is believed to be unidirectional and irreversible. The Rb family of proteins ( Rb, p107, and p130) regulates cell-cycle exit and differentiation during retinogenesis. Rb and p130 are redundantly expressed in the neurons of the inner nuclear layer (INL) of the retina. We have found that in the adult Rb; p130-deficient retinae p107 compensation prevents ectopic proliferation of INL neurons. However, p107 is haploinsufficient in this process. Differentiated Rb (-/-); p107(+/-); p130(-/-) horizontal interneurons re-entered the cell cycle, clonally expanded, and formed metastatic retinoblastoma. Horizontal cells were not affected in Rb+/-; p107(-/-); p130(-/-) or Rb-/-; p107(-/-); p130(+/-), retinae suggesting that one copy of Rb or p130 was sufficient to prevent horizontal proliferation. We hereby report that differentiated neurons can proliferate and form cancer while maintaining their differentiated state including neurites and synaptic connections.
引用
收藏
页码:378 / 390
页数:13
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