Journal
DEVELOPMENT
Volume 132, Issue 13, Pages 2943-2954Publisher
COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.01864
Keywords
Pkb gamma/Akt3 knockout; brain development; apoptosis
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Protein kinase B is implicated in many crucial cellular processes, such as metabolism, apoptosis and cell proliferation. In contrast to Pkb alpha and Pkb beta-deficient mice, Pkb gamma(-/-) mice are viable, show no growth retardation and display normal glucose metabolism. However, in adult Pkb gamma mutant mice, brain size and weight are dramatically reduced by about 25%. In vivo magnetic resonance imaging confirmed the reduction of Pkb gamma(-/-) brain volumes with a proportionally smaller ventricular system. Examination of the major brain structures revealed no anatomical malformations except for a pronounced thinning of white matter fibre connections in the corpus callosum. The reduction in brain weight of Pkb gamma(-/-) mice is caused, at least partially, by a significant reduction in both cell size and cell number. Our results provide novel insights into the physiological role of PKB gamma and suggest a crucial role in postnatal brain development.
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