21 research outputs found
Generation and Bioenergetic Profiles of Cybrids with East Asian mtDNA Haplogroups
Human mitochondrial DNA (mtDNA) variants and haplogroups may contribute to susceptibility to various diseases and pathological conditions, but the underlying mechanisms are not well understood. To address this issue, we established a cytoplasmic hybrid (cybrid) system to investigate the role of mtDNA haplogroups in human disease; specifically, we examined the effects of East Asian mtDNA genetic backgrounds on oxidative phosphorylation (OxPhos). We found that mtDNA single nucleotide polymorphisms such as m.489T>C, m.10398A>G, m.10400C>T, m.C16223T, and m.T16362C affected mitochondrial function at the level of mtDNA, mtRNA, or the OxPhos complex. Macrohaplogroup M exhibited higher respiratory activity than haplogroup N owing to its higher mtDNA content, mtRNA transcript levels, and complex III abundance. Additionally, haplogroup M had higher reactive oxygen species levels and NAD+/NADH ratios than haplogroup N, suggesting difference in mitonuclear interactions. Notably, subhaplogroups G2, B4, and F1 appeared to contribute significantly to the differences between haplogroups M and N. Thus, our cybrid-based system can provide insight into the mechanistic basis for the role of mtDNA haplogroups in human diseases and the effect of mtDNA variants on mitochondrial OxPhos function. In addition, studies of mitonuclear interaction using this system can reveal predisposition to certain diseases conferred by variations in mtDNA
Anti-oxidant polydatin (piceid) protects against substantia nigral motor degeneration in multiple rodent models of Parkinsonâs disease
Mitochondrial complex 1 activity measured by spectrophotometry is reduced across all brain regions in ageing and more specifically in neurodegeneration
Mitochondrial function, in particular complex 1 of the electron transport chain (ETC), has been shown to decrease during normal ageing and in neurodegenerative disease. However, there is some debate concerning which area of the brain has the greatest complex 1 activity. It is important to identify the pattern of activity in order to be able to gauge the effect of age or disease related changes. We determined complex 1 activity spectrophotometrically in the cortex, brainstem and cerebellum of middle aged mice (70â71 weeks), a cerebellar ataxic neurodegeneration model (pcd5J) and young wild type controls. We share our updated protocol on the measurements of complex1 activity and find that mitochondrial fractions isolated from frozen tissues can be measured for robust activity. We show that complex 1 activity is clearly highest in the cortex when compared with brainstem and cerebellum (p<0.003). Cerebellum and brainstem mitochondria exhibit similar levels of complex 1 activity in wild type brains. In the aged brain we see similar levels of complex 1 activity in all three-brain regions. The specific activity of complex 1 measured in the aged cortex is significantly decreased when compared with controls (p<0.0001). Both the cerebellum and brainstem mitochondria also show significantly reduced activity with ageing (p<0.05). The mouse model of ataxia predictably has a lower complex 1 activity in the cerebellum, and although reductions are measured in the cortex and brain stem, the remaining activity is higher than in the aged brains. We present clear evidence that complex 1 activity decreases across the brain with age and much more specifically in the cerebellum of the pcd5j mouse. Mitochondrial impairment can be a region specific phenomenon in disease, but in ageing appears to affect the entire brain, abolishing the pattern of higher activity in cortical regions
Carbon isotope composition and its evolution around the base of the Drumian Stage in Linzhou area, northern Henan
Carbon isotope stratigraphy is an important means to subdivide and correlate the Cambrian strata. Based on the carbon isotope analysis of the carbonate strata of LĂźtuogou Section, northern Henan Province, it is found the δ13C value of carbonate samples collected from the base of the Drumian Stage at LĂźtuogou Section, northern Henan, ranges from 3.1â° to -1.7â°, and the δ18O value ranges from -3.9â° to -9.4â°. No covariance exists between δ13C and δ18O, which implies that the carbon isotope composition is nearly stable. Value of δ13C around the base of the Drumian Stage consists of a negative excursion, the amplitude of the negative excursion is 3.0â°, and the minimum value of δ13C is -1.7â°, which occurs at the place 15 m below the first occurrence of trilobite protasaphiscus. The position and amplitude of the negative excursion are similar to those of the drum carbon isotope excursion (DICE) tested in the Wangcun Section, western Hunan, South China, and the Drum Mountains section in Utah, USA, which suggests that the DICE can be used as a global indicator for the correlation of the Drumian Stage. Furthermore, the cyan shale with thin limestone at the position of minimum δ13C overlies the oolitic limestone; therefore, DICE occurs in the transgressive succession in the early Miaolingian
Carbon-Isotope Excursions Recorded in the Cambrian System, South China: Implications for Mass Extinctions and Sea-Level Fluctuations
Cambrian carbonates with abundant fossils of agnostoid trilobites deposited on the southern slope (Jiangnan slope belt) of the Yangtze Platform and in the Jiangnan deepwater basin are well exposed in the Wangcun Section of western Hunan, South China, and in the Duibian A Section of western Zhejiang, southeastern China, respectively. To better understand the response of carbon-isotope excursions to depositional environment changes, mass extinctions and eustatic events, we collected 530 carbonate samples in fresh roadcut exposures of the two measured sections for analysis of carbon and oxygen isotopic compositions. Data of δ13C from the Wangcun Section, western Hunan, South China, demonstrate that the Cambrian carbon-isotope profile includes three remarkable positive excursions CPEwc-1, 2, 3 in the Upper Series 2, in the Lower and in the Middle Furongian Series. Three distinctive negative excursions CNEwc-1, 2, 3 were separately tested in the Lower Terreneuvian Series, Lower Series 3 and in the Upper Furongian Series. Similarly, in the corresponding horizons in the Duibian A Section, Zhejiang Province, southeastern China, three positive excursions CPEdb-1, 2, 3 and three negative excursions CNEdb-1, 2, 3 also have been discovered. We interpret these significant carbon-isotope excursions as being associated with enhanced biogenic productivity, mass extinctions and eustatic events
Simultaneous Improvement of Efficiency and Lifetime of Quantum Dot Light-Emitting Diodes with a Bilayer Hole Injection Layer Consisting of PEDOT:PSS and Solution-Processed WO<sub>3</sub>
Even though chemically
stable metal oxides (MOs), as substitutes for polyÂ(3,4-ethylenedioxythiophene):polystyrene
sulfonate (PEDOT:PSS), have been successfully adopted for improving
device stability in solution-processed quantum dot light-emitting
diodes (QLEDs), the efficiencies of QLEDs are at a relatively low
level. In this work, a novel architecture of QLEDs has been introduced,
in which inorganic/organic bilayer hole injection layers (HILs) were
delicately designed by inserting an amorphous WO<sub>3</sub> interlayer
between PEDOT:PSS and the indium tin oxide anode. As a result, the
efficiency and operational lifetime of QLEDs were improved simultaneously.
The results show that the novel architecture QLEDs relative to conventional
PEDOT:PSS-based QLEDs have an enhanced external quantum efficiency
by a factor of 50%, increasing from 8.31 to 12.47%, meanwhile exhibit
a relatively long operational lifetime (12â551 h) and high
maximum brightness (>40â000 cd m<sup>â2</sup>) resulting
from a better pathway for hole injection with staircase energy-level
alignment of the HILs and reduction of surface roughness. Our results
demonstrate that the novel architecture QLEDs using bilayer MO/PEDOT:PSS
HILs can achieve long operational lifetime without sacrificing efficiency
Systematic analysis of a mitochondrial diseaseâcausing ND6 mutation in mitochondrial deficiency
Abstract Background The m.14487T>C mutation is recognized as a diagnostic mutation of mitochondrial disease during the past 16Â years, emerging evidence suggests that mutant loads of m.14487T>C and disease phenotype are not closely correlated. Methods Immortalized lymphocytes were generated by coculturing the EpsteinâBarr virus and lymphocytes from m.14487T>C carrier Chinese patient with Leigh syndrome. Fifteen cytoplasmic hybrid (cybrid) cell lines were generated by fusing mtDNA lacking 143B cells with platelets donated by patients. Mitochondrial function was systematically analyzed at transcriptomic, metabolomic, and biochemical levels. Results Unlike previous reports, we found that the assembly of mitochondrial respiratory chain complexes, mitochondrial respiration, and mitochondrial OXPHOS function was barely affected in cybrid cells carrying homoplastic m.14487T>C mutation. Mitochondrial dysfunction associated transcriptomic and metabolomic reprogramming were not detected in cybrid carrying homoplastic m.14487T>C. However, we found that mitochondrial function was impaired in patientâderived immortalized lymphocytes. Conclusion Our data revealed that m.14487T>C mutation is insufficient to cause mitochondrial deficiency; additional modifier genes may be involved in m.14487T>Câassociated mitochondrial disease. Our results further demonstrated that a caution should be taken by solely use of m.14487T>C mutation for molecular diagnosis of mitochondrial disease
Phosphine-Free Synthesis from 1D Pb(OH)Cl Nanowires to 0D and 1D PbSe Nanocrystals
In this paper, we report a new phosphine-free,
low-cost, low-temperature
colloidal method of controlled synthesis of PbSe nanocrystals in both
zero-dimension (0D) and one-dimension (1D). Different from the widely
used âhot injectionâ method and ânonprecursor
injectionâ method, the novelty of this new method is that it
does not require a nucleation process. Instead, high-quality presynthesized
1D PbÂ(OH)Cl nanowires (âź80 to âź160 nm in diameter) can
be directly used as a Pb precursor and reacted with a Se precursor
to form monodisperse dot-shaped 0D cubic PbSe and 1D orthorhombic
PbSe nanowires. 0D cubic PbSe nanocrystals begin to form at elevated
temperatures after the Se precursor is added to react with PbÂ(OH)ÂCl
nanowires. By prolonging the reaction time for 3 h, good self-assembled
0D cubic PbSe nanocrystals can be synthesized with an average diameter
of about 15 nm. Furthermore, such method has been demonstrated to
synthsize high-quality 1D PbSe nanowires successfully with temperature
as low as 110 °C. 1D PbSe nanowires possess a mean diameter of
15â24 nm with the shortest and longest length from 600 nm to
5 Îźm. The only sharp and strong peak, which is consistent with
characteristic peaks of orthorhombic PbSe, indicates that the nanowiresâ
elongation axis is in the [111] direction, and 0D cubic PbSe nanocrystals
change to 1D orthorhombic PbSe nanowires completely