Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Subscribe

Sci. STKE, 28 November 2006
Vol. 2006, Issue 363, p. tw400
[DOI: 10.1126/stke.3632006tw400]

EDITORS' CHOICE

Neuroscience Males Afraid, Females Brave

Nancy R. Gough

Science's STKE, AAAS, Washington, DC 20005, USA

There are different kinds of memories. In mice, differences have been noted in contextual fear memory formation and spatial memory formation, although both forms of memory appear to involve a calcium signal and the activation of calcium/calmodulin-dependent kinases (CaMKs). In mice, there are two isoforms of CaMK that have been implicated in memory formation (CaMKI and CaMKIV) and two upstream kinases that phosphorylate CaMK (CaM kinase kinases: CaMKK{alpha} and CaMKKbeta). CaMKKbeta has been implicated in spatial memory formation, and CaMKIV has been implicated in long-term potentiation and fear conditioning. Two groups, Blaeser et al. and Mizuno et al., created mice deficient in CaMKK{alpha} function and found that the mice showed normal spatial memory, normal motor activity, and normal sensory perception; however, male mice were impaired in the formation of contextual fear memories. Synaptic transmission was not impaired in the CamKK{alpha}-deficient mice, nor was formation of hippocampal long-term potentiation. Blaeser et al. showed that, compared with wild-type mice, the CamKK{alpha}-deficient male mice exhibited decreased phosphorylation of CaMKIV and the transcriptional regulator CREB (a substrate of CaMKIV) in response to fear conditioning. Phosphorylation of CREB under basal conditions was increased in the mutant mice in certain brain regions; however, the fear-induced increases in phosphorylation were absent. Mizuno et al. investigated memory formation in both male and female mice deficient for CaMKK{alpha} and noted that females did not show impairment of contextual fear conditioning. (It was known that female mice tend to exhibit contextual fear conditioning to a lesser extent than do male mice.) In wild-type mice, contextual fear conditioning promoted an increase in brain-derived neurotrophic factor (BDNF) in males only and a decrease in BDNF in females (transcript abundance was measured by real-time polymerase chain reaction). In the CaMKK{alpha}-deficient mice, the increase in BDNF in males was compromised, but the decrease in females was unaffected. The gene encoding BDNF is a CREB target; however, expression of another gene regulated by CREB, the gene encoding nerve growth factor-inducible gene B (NGF-1B), was increased in response to fear conditioning in both males and females and was not affected by lack of CaMKK{alpha}. Thus, in addition to specific forms of memory requiring specific signaling cascades, there is an additional gender-specific layer of regulation.

F. Blaeser, M. J. Sanders, N. Truong, S. Ko, L. J. Wu, D. F. Wozniak. M. S. Fanselow, M. Zhuo, T. A. Chatila, Long-term memory deficits in Pavlovian fear conditioning in Ca2+/calmodulin kinase kinase {alpha}-deficient mice. Mol. Cell. Biol. 26, 9105-9115 (2006). [Abstract] [Full Text]

K. Mizuno, L. Ris, A. Sánchez-Capelo, E. Godaux, K. P. Giese, Ca2+/calmodulin kinase kinase {alpha} is dispensable for brain development but is required for distinct memories in male, though not in female, mice. Mol. Cell. Biol. 26, 9094-9104 (2006). [Abstract] [Full Text]

Citation: N. R. Gough, Males Afraid, Females Brave. Sci. STKE 2006, tw400 (2006).


To Advertise     Find Products


Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882