And Amino Acids in the Culture MediaAmmonium was measured on an Integra automatic analyzer (Roche); glucose, lactate and lactate dehydrogenase (LDH) were measured on a Modular automatic analyzer (Roche); free amino acids were analyzed on a Beckman 6300 amino acid analyzer; as described previously [17]; lactate and pyruvate for measurement of the lactate/pyruvate ratio were measured by GC/MS (HP 6890 N, Agilent Technologies).Expression of GCDH in Brain CellsNon-radioactive in situ hybridization for Gcdh mRNA, making use of digoxygenin-labeled riboprobes transcribed from GcdhBrain Cell Damage in Glutaric Aciduria Type Ibuy Nobiletin Figure 2. Effects of GA and 3-OHGA on neurons. (Left panel) Immunohistochemical staining for phosphorylated medium weight neurofilament (p-NFM) on cryosections of cultures derived from protocol A (DIV 8) and protocol B (DIV 14). Scale bar: 100 mm. (Right panel) Representative western blots with data quantification of whole-cell lysates for p-NFM for protocol A (DIV 8, above) and protocol B (DIV 14, below). Actin was used as a loading control. The quantifications of p-NFM are expressed as percentage of respective controls. The values represent the mean 6 SD from 3 replicates taken from 2 independent experiments. doi:10.1371/journal.pone.0053735.gOligodendrocytes. 3-OHGA-exposure, and to a lesser extent GA-exposure, resulted in a substantial decrease of MBP staining 26001275 under protocol B (DIV 14) (Figure 4, left panel). Western blot analysis confirmed decreased MBP expression under the same conditions (Figure 4, right panel). We could not see any effect for MBP staining in protocol A since the expression of MBP protein is very low in the immature developmental stages (data not shown). In order to discriminate whether the observed signal loss is a result of oligodendrocytic death or altered differentiation and/or myelination, we performed immunohistochemical staining for GalC, one of the earliest markers of oligodendrocytes. Only slight reduction of GalC signal was observed in the cultures treated with 3-OHGA on DIV 8 (Figure 4, left panel) and no difference was seen with any of the two metabolites on DIV 14 (data not shown). Microglia. The presence of microglia was tested by immunostaining for isolectin B4 at DIV 8. No interesting changes were observed (data not shown).observed in the medium of treated DIV 14 cultures. Lactate release into medium remained unchanged in immature DIV 8 cultures (Figure 5B). The lactate/pyruvate ratio was increased in the medium of DIV 14 3-OHGA-exposed cultures (55.4 under 1 mM 3-OHGA versus 26.2 in controls; mean of duplicates for each condition). Ammonium and Glutamine. A massive increase in ammonium concentrations was measured in the culture media after exposure to 3-OHGA and GA under both protocols (DIV 8 and 14) (Figure 5C). Among amino acids measured in the culture medium, a significant decrease was observed on glutamine levels in all cultures exposed to GA and 3-OHGA under both protocols (Figure 5D).Increased Cell Death in Developing Brain Cells After Exposure to GA and 3-OHGALactate dehydrogenase (LDH) was measured in culture medium and was significantly increased after 3-OHGA- and GA-exposure in both protocols (DIV 8 and DIV 14) (Figure 6C). This observation indicated an increase of cell death in these cultures. To evaluate cell death, we performed TUNEL, DAPI and activated caspase-3 immunofluorescence staining. DAPI staining did not show an increased MedChemExpress Nafarelin appearance of nuclear fragmentation and.And Amino Acids in the Culture MediaAmmonium was measured on an Integra automatic analyzer (Roche); glucose, lactate and lactate dehydrogenase (LDH) were measured on a Modular automatic analyzer (Roche); free amino acids were analyzed on a Beckman 6300 amino acid analyzer; as described previously [17]; lactate and pyruvate for measurement of the lactate/pyruvate ratio were measured by GC/MS (HP 6890 N, Agilent Technologies).Expression of GCDH in Brain CellsNon-radioactive in situ hybridization for Gcdh mRNA, making use of digoxygenin-labeled riboprobes transcribed from GcdhBrain Cell Damage in Glutaric Aciduria Type IFigure 2. Effects of GA and 3-OHGA on neurons. (Left panel) Immunohistochemical staining for phosphorylated medium weight neurofilament (p-NFM) on cryosections of cultures derived from protocol A (DIV 8) and protocol B (DIV 14). Scale bar: 100 mm. (Right panel) Representative western blots with data quantification of whole-cell lysates for p-NFM for protocol A (DIV 8, above) and protocol B (DIV 14, below). Actin was used as a loading control. The quantifications of p-NFM are expressed as percentage of respective controls. The values represent the mean 6 SD from 3 replicates taken from 2 independent experiments. doi:10.1371/journal.pone.0053735.gOligodendrocytes. 3-OHGA-exposure, and to a lesser extent GA-exposure, resulted in a substantial decrease of MBP staining 26001275 under protocol B (DIV 14) (Figure 4, left panel). Western blot analysis confirmed decreased MBP expression under the same conditions (Figure 4, right panel). We could not see any effect for MBP staining in protocol A since the expression of MBP protein is very low in the immature developmental stages (data not shown). In order to discriminate whether the observed signal loss is a result of oligodendrocytic death or altered differentiation and/or myelination, we performed immunohistochemical staining for GalC, one of the earliest markers of oligodendrocytes. Only slight reduction of GalC signal was observed in the cultures treated with 3-OHGA on DIV 8 (Figure 4, left panel) and no difference was seen with any of the two metabolites on DIV 14 (data not shown). Microglia. The presence of microglia was tested by immunostaining for isolectin B4 at DIV 8. No interesting changes were observed (data not shown).observed in the medium of treated DIV 14 cultures. Lactate release into medium remained unchanged in immature DIV 8 cultures (Figure 5B). The lactate/pyruvate ratio was increased in the medium of DIV 14 3-OHGA-exposed cultures (55.4 under 1 mM 3-OHGA versus 26.2 in controls; mean of duplicates for each condition). Ammonium and Glutamine. A massive increase in ammonium concentrations was measured in the culture media after exposure to 3-OHGA and GA under both protocols (DIV 8 and 14) (Figure 5C). Among amino acids measured in the culture medium, a significant decrease was observed on glutamine levels in all cultures exposed to GA and 3-OHGA under both protocols (Figure 5D).Increased Cell Death in Developing Brain Cells After Exposure to GA and 3-OHGALactate dehydrogenase (LDH) was measured in culture medium and was significantly increased after 3-OHGA- and GA-exposure in both protocols (DIV 8 and DIV 14) (Figure 6C). This observation indicated an increase of cell death in these cultures. To evaluate cell death, we performed TUNEL, DAPI and activated caspase-3 immunofluorescence staining. DAPI staining did not show an increased appearance of nuclear fragmentation and.
