D-SERINE CONTRIBUTES TO β-AMYLOID-DEPENDENT PATHOPHYSIOLOGYIN ALZHEIMER’S DISEASE

International audienceB fEPSP/PFV ra>o 0 0,2 0,4 0,6 0,8 1 1,2 1,4 1,6 WT 5xFAD 5xFAD/SR-/-+ D-s e ri n e + D-s e ri n e + D-s e ri n e Key regulators of the structural and funcFonal brain plasFcity, the N-methyl-D-aspartate subtype of glutamate receptors (NMDARs) requires the binding of the co-agonist D-serine to be acFvated. In Alzheimer's disease (AD), soluble oligomers of the beta-amyloid pepFde (Aßo) affect NMDARs possibly through mechanisms involving changes in D-serine levels since Aßo sFmulate in vitro the producFon of the co-agonist. In this study, we asked whether D-serine contributes in vivo to morpho-funcFonal NMDAR-related deregulaFons mediated by Aßo. Behavioral analysis combined to electrophysiological recordings at CA1/CA3 hippocampal synapses have been thus conducted in the 5xFAD transgenic mice model of amyloïdogenesis displaying marked increase in Aßo rates and compared to 5xFAD animals in which the homozygous gene of the serine racemase (SR) that synthesizes D-serine, has been jointly invalidated. Our results therefore show that deleFon of serine racemase prevents memory-related behavioral deficits observed in mice with prominent features of amyloidogenesis as well as impairment of NMDAR-dependent funcFonal plasFcity, suggesFng a significant contribuFon of D-serine in NMDAR-dependent β-amyloid-related pathophysiology of Alzheimer's disease. EXPERIMENTAL PROCEDURES 1) Behavioral analysis: 8-min spontaneous alternaFon test was performed in a Y maze apparatus to assess working memory performances in 10-12 months of aged mice. Successive entry of the three arms of the maze was considered as an alternaFon. The percentage of alternaFon was calculated as follows: number of alternaFons / (total number of arms visited-2) x 100. 2) Electrophysiology: Hippocampal slices (400 µm thickness) were cut from two groups of WT, 5xFAD/SR +/+ and 5xFAD/SR-/-mice aged 3-4 or 10-12 months. Field excitatory postsynapFc potenFals (fEPSPs) and presynapFc fiber volley (PFV) were extracellularly recorded in CA1 stratum radiatum aner electrical sFmulaFon of Schaffer collaterals. Input/output curves of the fEPSP/PFV raFo of isolated NMDAr-mediated fEPSPs were constructed in a low magnesium medium supplemented with the non-NMDAr antagonist NBQX (10µM) before and 15 min aner addiFon of D-serine (100 µM). High frequency (HFS)-induced long-term potenFaFon (LTP) was studied in control medium aner tetanic sFmulaFon consisFng in one train at 100 Hz delivered for 1 sec. TesFng sFmulaFon was then resumed for 60 min aner HFS. 3) Semi-quanFtaFve immunoblopng analysis: Hippocampal Fssue was homogenized in protein lysis buffer. The membranes were probed with anFbodiesaginst GluN1 (1:750

D-­‐SERINE IS INVOLVED IN THE β-­‐AMYLOID-­‐RELATED PATHOPHYSIOLOGYIN ALZHEIMER’S DISEASE

International audienc

IMPACT OF D-SERINE DEPLETION IN THE β-AMYLOID CASCADERELATED TO ALZHEIMER’S DISEASE

International audienceD-serine, as a co-agonist of N-methyl-D-aspartate subtype of glutamate receptors (NMDAR), is a key regulator of their activation and hence involves in functional brain plasticity and memory process. The homeostasis of these receptors is affected by soluble oligomers of the beta-amyloid peptide (Aß) in Alzheimer´s disease (AD). In the course of AD, early functional dysregulations of NMDAR are well known, even though contribution of D-serine remains so far to be determined. In 3-4 month-old transgenic mice model of amyloïdogenesis (5xFAD) showing marked increase in Aß rates and apparent unaffected D-serine levels, extracellular electrophysiological recordings reveal impaired NMDAR-dependent long-term potentiation at CA1/CA3 hippocampal synapses, without significant changes in basal synaptic transmission. This deficit persists at 12 month of age when amyloid deposits are present with concomitant disabilities in cognitive functions. Generating 5xFAD mice with depletion of D-serine (through invalidation of the synthesis enzyme: Serine Racemase), we observed that these functional alterations and the long-term behavioral impairment were prevented whereas Aßo rates remain significantly elevated and comparable to 5xAFD mice. Therefore, these results provide convincing evidence for a critical and transient involvement of D-serine in hippocampal network dysfunctions and related cognitive disabilities driven by increased amyloidogenesis

Biological-like vesicular structures self-assembled from DNA-block copolymers

The polymer modification of short nucleotide sequences has been achieved for future use as self-assembled biologically active structures with sizes in the nanometre range. Co-assembly of the resulting DNA-based amphiphilic block copolymers with native proteins demonstrates the self-assembly of biological-like vesicular structures

Differential attraction and repulsion of Staphylococcus aureus and Pseudomonas aeruginosa on molecularly smooth titanium films

Magnetron sputtering techniques were used to prepare molecularly smooth titanium thin films possessing an average roughness between 0.18 nm and 0.52 nm over 5 μm × 5 μm AFM scanning areas. Films with an average roughness of 0.52 nm or lower were found to restrict the extent of P. aeruginosa cell attachment, with less than 0.5% of all available cells being retained on the surface. The attachment of S. aureus cells was also limited on films with an average surface roughness of 0.52 nm, however they exhibited a remarkable propensity for attachment on the nano-smoother 0.18 nm average surface roughness films, with the attachment density being almost twice as great as that observed on the nano-rougher film. The difference in attachment behaviour can be attributed to the difference in morphology of the rod-shaped P. aeruginosa compared to the spherical S. aureus cells

Minimum Information about a Biosynthetic Gene cluster

A wide variety of enzymatic pathways that produce specialized metabolites in bacteria, fungi and plants are known to be encoded in biosynthetic gene clusters. Information about these clusters, pathways and metabolites is currently dispersed throughout the literature, making it difficult to exploit. To facilitate consistent and systematic deposition and retrieval of data on biosynthetic gene clusters, we propose the Minimum Information about a Biosynthetic Gene cluster (MIBiG) data standard.Chemistry and Chemical Biolog

La cyclopropane fatty acid synthase d'Escherichia coli (études mécanistiques et identification de nouveaux inhibiteurs)

PARIS-BIUSJ-Thèses (751052125) / SudocPARIS-BIUSJ-Physique recherche (751052113) / SudocSudocFranceF

D-serine in physiological and pathological brain aging

International audienc

D-SERINE CONTRIBUTES TO β-AMYLOID-DEPENDENT PATHOPHYSIOLOGYIN ALZHEIMER’S DISEASE

International audienceB fEPSP/PFV ra>o 0 0,2 0,4 0,6 0,8 1 1,2 1,4 1,6 WT 5xFAD 5xFAD/SR-/-+ D-s e ri n e + D-s e ri n e + D-s e ri n e Key regulators of the structural and funcFonal brain plasFcity, the N-methyl-D-aspartate subtype of glutamate receptors (NMDARs) requires the binding of the co-agonist D-serine to be acFvated. In Alzheimer's disease (AD), soluble oligomers of the beta-amyloid pepFde (Aßo) affect NMDARs possibly through mechanisms involving changes in D-serine levels since Aßo sFmulate in vitro the producFon of the co-agonist. In this study, we asked whether D-serine contributes in vivo to morpho-funcFonal NMDAR-related deregulaFons mediated by Aßo. Behavioral analysis combined to electrophysiological recordings at CA1/CA3 hippocampal synapses have been thus conducted in the 5xFAD transgenic mice model of amyloïdogenesis displaying marked increase in Aßo rates and compared to 5xFAD animals in which the homozygous gene of the serine racemase (SR) that synthesizes D-serine, has been jointly invalidated. Our results therefore show that deleFon of serine racemase prevents memory-related behavioral deficits observed in mice with prominent features of amyloidogenesis as well as impairment of NMDAR-dependent funcFonal plasFcity, suggesFng a significant contribuFon of D-serine in NMDAR-dependent β-amyloid-related pathophysiology of Alzheimer's disease. EXPERIMENTAL PROCEDURES 1) Behavioral analysis: 8-min spontaneous alternaFon test was performed in a Y maze apparatus to assess working memory performances in 10-12 months of aged mice. Successive entry of the three arms of the maze was considered as an alternaFon. The percentage of alternaFon was calculated as follows: number of alternaFons / (total number of arms visited-2) x 100. 2) Electrophysiology: Hippocampal slices (400 µm thickness) were cut from two groups of WT, 5xFAD/SR +/+ and 5xFAD/SR-/-mice aged 3-4 or 10-12 months. Field excitatory postsynapFc potenFals (fEPSPs) and presynapFc fiber volley (PFV) were extracellularly recorded in CA1 stratum radiatum aner electrical sFmulaFon of Schaffer collaterals. Input/output curves of the fEPSP/PFV raFo of isolated NMDAr-mediated fEPSPs were constructed in a low magnesium medium supplemented with the non-NMDAr antagonist NBQX (10µM) before and 15 min aner addiFon of D-serine (100 µM). High frequency (HFS)-induced long-term potenFaFon (LTP) was studied in control medium aner tetanic sFmulaFon consisFng in one train at 100 Hz delivered for 1 sec. TesFng sFmulaFon was then resumed for 60 min aner HFS. 3) Semi-quanFtaFve immunoblopng analysis: Hippocampal Fssue was homogenized in protein lysis buffer. The membranes were probed with anFbodiesaginst GluN1 (1:750