Abstract:
:Adult-born granule cells in the dentate gyrus of the rodent hippocampus are important for memory formation and mood regulation, but the cellular mechanism underlying their polarized development, a process critical for their incorporation into functional circuits, remains unknown. We found that deletion of the serine-threonine protein kinase LKB1 or overexpression of dominant-negative LKB1 reduced the polarized initiation of the primary dendrite from the soma and disrupted its oriented growth toward the molecular layer. This abnormality correlated with the dispersion of Golgi apparatus that normally accumulated at the base and within the initial segment of the primary dendrite, and was mimicked by disrupting Golgi organization via altering the expression of Golgi structural proteins GM130 or GRASP65. Thus, besides its known function in axon formation in embryonic pyramidal neurons, LKB1 plays an additional role in regulating polarized dendrite morphogenesis in adult-born granule cells in the hippocampus.
journal_name
Proc Natl Acad Sci U S Aauthors
Huang W,She L,Chang XY,Yang RR,Wang L,Ji HB,Jiao JW,Poo MMdoi
10.1073/pnas.1321454111subject
Has Abstractpub_date
2014-01-07 00:00:00pages
469-74issue
1eissn
0027-8424issn
1091-6490pii
1321454111journal_volume
111pub_type
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