scholarly journals Rho GTPase activity in the honey bee mushroom bodies is correlated with age and foraging experience

2012 ◽  
Vol 58 (2) ◽  
pp. 228-234 ◽  
Author(s):  
Scott E. Dobrin ◽  
Susan E. Fahrbach
2012 ◽  
Vol 72 (2) ◽  
pp. 153-166 ◽  
Author(s):  
Claudia C. Lutz ◽  
Sandra L. Rodriguez-Zas ◽  
Susan E. Fahrbach ◽  
Gene E. Robinson

2008 ◽  
Vol 77 (1) ◽  
pp. 348-359 ◽  
Author(s):  
Aimee M. deCathelineau ◽  
Gary M. Bokoch

ABSTRACT Anthrax lethal factor (LF), secreted by Bacillus anthracis, interacts with protective antigen to form a bipartite toxin (lethal toxin [LT]) that exerts pleiotropic biological effects resulting in subversion of the innate immune response. Although the mitogen-activated protein kinase kinases (MKKs) are the major intracellular protein targets of LF, the pathology induced by LT is not well understood. The statin family of HMG-coenzyme A reductase inhibitors have potent anti-inflammatory effects independent of their cholesterol-lowering properties, which have been attributed to modulation of Rho family GTPase activity. The Rho GTPases regulate vesicular trafficking, cytoskeletal dynamics, and cell survival and proliferation. We hypothesized that disruption of Rho GTPase function by statins might alter LT action. We show here that statins delay LT-induced death and MKK cleavage in RAW macrophages and that statin-mediated effects on LT action are attributable to disruption of Rho GTPases. The Rho GTPase-inactivating toxin, toxin B, did not significantly affect LT binding or internalization, suggesting that the Rho GTPases regulate trafficking and/or localization of LT once internalized. The use of drugs capable of inhibiting Rho GTPase activity, such as statins, may provide a means to attenuate intoxication during B. anthracis infection.


2008 ◽  
Vol 31 (5) ◽  
pp. 491-499 ◽  
Author(s):  
Galina V. Shurin ◽  
Irina L. Tourkova ◽  
Michael R. Shurin

2021 ◽  
pp. jeb.238899
Author(s):  
Mallory A. Hagadorn ◽  
Makenna M. Johnson ◽  
Adam R. Smith ◽  
Marc A. Seid ◽  
Karen M. Kapheim

In social insects, changes in behavior are often accompanied by structural changes in the brain. This neuroplasticity may come with experience (experience-dependent) or age (experience-expectant). Yet, the evolutionary relationship between neuroplasticity and sociality is unclear, because we know little about neuroplasticity in the solitary relatives of social species. We used confocal microscopy to measure brain changes in response to age and experience in a solitary halictid bee (Nomia melanderi). First, we compared the volume of individual brain regions among newly-emerged females, laboratory females deprived of reproductive and foraging experience, and free-flying, nesting females. Experience, but not age, led to significant expansion of the mushroom bodies—higher-order processing centers associated with learning and memory. Next, we investigated how social experience influences neuroplasticity by comparing the brains of females kept in the laboratory either alone or paired with another female. Paired females had significantly larger olfactory regions of the mushroom bodies. Together, these experimental results indicate that experience-dependent neuroplasticity is common to both solitary and social taxa, whereas experience-expectant neuroplasticity may be an adaptation to life in a social colony. Further, neuroplasticity in response to social chemical signals may have facilitated the evolution of sociality.


2014 ◽  
pp. 283-292
Author(s):  
James B. Bliska ◽  
Gloria I. Viboud

2007 ◽  
Vol 8 (6) ◽  
pp. 569-577 ◽  
Author(s):  
Ashleigh Hodges ◽  
Katherine Sharrocks ◽  
Mariola Edelmann ◽  
Dilair Baban ◽  
Arnaud Moris ◽  
...  

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