Sorting Out Frontotemporal Dementia?

نویسندگان

  • Jada Lewis
  • Todd E. Golde
چکیده

Mutations within the granulin (GRN) gene that encodes progranulin (PGRN) cause the neurodegenerative disease frontotemporal lobar degeneration with ubiquitin inclusions (FTLD-U). The receptor for PGRN in the CNS has not been previously identified. In this issue of Neuron, Hu and colleagues identify Sortilin (SORT1) as a key neuronal receptor for PGRN that facilitates its endocytosis and regulates PGRN levels in vitro and in vivo.

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عنوان ژورنال:
  • Neuron

دوره 68  شماره 

صفحات  -

تاریخ انتشار 2010