PMID- 22808101 OWN - NLM STAT- MEDLINE DCOM- 20130319 LR - 20211021 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 7 IP - 7 DP - 2012 TI - Evaluation of gene, protein and neurotrophin expression in the brain of mice exposed to space environment for 91 days. PG - e40112 LID - 10.1371/journal.pone.0040112 [doi] LID - e40112 AB - Effects of 3-month exposure to microgravity environment on the expression of genes and proteins in mouse brain were studied. Moreover, responses of neurobiological parameters, nerve growth factor (NGF) and brain derived neurotrophic factor (BDNF), were also evaluated in the cerebellum, hippocampus, cortex, and adrenal glands. Spaceflight-related changes in gene and protein expression were observed. Biological processes of the up-regulated genes were related to the immune response, metabolic process, and/or inflammatory response. Changes of cellular components involving in microsome and vesicular fraction were also noted. Molecular function categories were related to various enzyme activities. The biological processes in the down-regulated genes were related to various metabolic and catabolic processes. Cellular components were related to cytoplasm and mitochondrion. The down-regulated molecular functions were related to catalytic and oxidoreductase activities. Up-regulation of 28 proteins was seen following spaceflight vs. those in ground control. These proteins were related to mitochondrial metabolism, synthesis and hydrolysis of ATP, calcium/calmodulin metabolism, nervous system, and transport of proteins and/or amino acids. Down-regulated proteins were related to mitochondrial metabolism. Expression of NGF in hippocampus, cortex, and adrenal gland of wild type animal tended to decrease following spaceflight. As for pleiotrophin transgenic mice, spaceflight-related reduction of NGF occurred only in adrenal gland. Consistent trends between various portions of brain and adrenal gland were not observed in the responses of BDNF to spaceflight. Although exposure to real microgravity influenced the expression of a number of genes and proteins in the brain that have been shown to be involved in a wide spectrum of biological function, it is still unclear how the functional properties of brain were influenced by 3-month exposure to microgravity. FAU - Santucci, Daniela AU - Santucci D AD - Behavioural Neuroscience Section, Cellular Biology and Neuroscience Department, Istituto Superiore di Sanita, Rome, Italy. FAU - Kawano, Fuminori AU - Kawano F FAU - Ohira, Takashi AU - Ohira T FAU - Terada, Masahiro AU - Terada M FAU - Nakai, Naoya AU - Nakai N FAU - Francia, Nadia AU - Francia N FAU - Alleva, Enrico AU - Alleva E FAU - Aloe, Luigi AU - Aloe L FAU - Ochiai, Toshimasa AU - Ochiai T FAU - Cancedda, Ranieri AU - Cancedda R FAU - Goto, Katsumasa AU - Goto K FAU - Ohira, Yoshinobu AU - Ohira Y LA - eng SI - GEO/GSE32077 PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20120709 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) SB - IM MH - Adrenal Glands/metabolism MH - Animals MH - Brain/*metabolism MH - Brain-Derived Neurotrophic Factor/genetics/metabolism MH - Down-Regulation/genetics MH - *Extraterrestrial Environment MH - *Gene Expression Regulation MH - Male MH - Mice MH - Mice, Inbred C57BL MH - Molecular Sequence Annotation MH - Nerve Growth Factors/*genetics/*metabolism MH - *Space Flight MH - Time Factors MH - Up-Regulation/genetics PMC - PMC3392276 COIS- Competing Interests: Toshimasa Ochiai is employed by Mitsubishi Heavy Industries. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials, as detailed online in the guide for authors. EDAT- 2012/07/19 06:00 MHDA- 2013/03/21 06:00 PMCR- 2012/07/09 CRDT- 2012/07/19 06:00 PHST- 2012/05/01 00:00 [received] PHST- 2012/05/31 00:00 [accepted] PHST- 2012/07/19 06:00 [entrez] PHST- 2012/07/19 06:00 [pubmed] PHST- 2013/03/21 06:00 [medline] PHST- 2012/07/09 00:00 [pmc-release] AID - PONE-D-12-12767 [pii] AID - 10.1371/journal.pone.0040112 [doi] PST - ppublish SO - PLoS One. 2012;7(7):e40112. doi: 10.1371/journal.pone.0040112. Epub 2012 Jul 9.