Examination of osteoarthritis for age-at-death estimation in a modern population

Age estimation techniques have utilized cranial suture closure, the sternal rib ends, the auricular surface, and the pubic symphysis, each with varying degrees of success. Although recent research has attempted to advance methodologies for age estimation, little progress has been made in discerning forensic age ranges that are beyond general estimates, especially in the old adult (50+) cohort. Since the accuracy of current aging methods decreases as chronological age increases, degenerative changes within the skeleton could potentially yield useful data for establishing and narrowing age estimates for older individuals, especially where only limited or fragmentary remains are recovered. The purpose of the present study was to conduct a visual examination of joint surfaces typically found to be affected by osteoarthritis (OA) by the fourth decade of life using a modified version of the OA scoring system proposed by Buikstra and Ubelaker (1994). According to archaeological, forensic, and clinical research, OA is most commonly found in the shoulder, hip, and knee, making these joints ideal for use in the present study. Within these three joints, ten osseous surfaces were examined: the acromial facet of the scapula, the glenoid fossa of the scapula, the lateral clavicle, the humeral head, the acetabulum of the os coxa, the femoral head, the medial and lateral femoral condyles, and the medial and lateral facets of the patella. Evidence of lipping, surface porosity, osteophyte formation, and eburnation were recorded on an ordinal scale, along with the percentage of the joint surface that was covered by each of the aforementioned traits. The data gathered from this examination were used to create a composite scoring system for age–at–death estimation using a modern North American sample of 206 White individuals from the W. M. Bass Donated Skeletal Collection and the Boston University Donated Osteological Collection. Significance testing indicated that sex differences were not present in the current analysis. A paired-sample t–test determined that the sample was affected with statistically significant levels of bilateral asymmetry. In addition, the current method is affected by low levels of intraobserver error, with only 5% of the sample being affected. Pearson's and Spearman's correlation coefficient were used to examine the relationship between a selected variable and age. The results of the present study indicate that OA has a positive correlation with age, although some joints show weaker associations than others. The right shoulder showed the highest correlation with age (r = 0.776, rs = 0.769; p < 0.01), followed closely by the left shoulder (r = 0.753, rs = 0.753; p < 0.01). The next highest correlation with age was observed for the left knee (r = 0.545, rs = 0.568; p < 0.01), followed by the right knee (r = 0.459, rs = 0.459; p < 0.01). The lowest correlation was observed in the left hip (r = 0.414, rs = 0.377; p < 0.01) and right hip (r = 0.476, rs = 0.377; p < 0.01). Data from multiple joint surfaces were combined for statistical analysis to create composite variables for each joint. The composite variables are combinations of traits for each joint that stepwise regression demonstrated as the best indictors for narrowing prediction intervals. This created a series of composite scores for the left shoulder, right shoulder, left hip, right hip, left knee and right knee. Individual prediction intervals at the 90% confidence interval were generated to create age ranges for each composite score. The mean age and frequency of each composite score was also recorded. This multifactorial approach demonstrated that the left and right shoulders provided the narrowest prediction intervals and also possessed the highest predictive power for estimating age-at-death. Relative predictive power was determined using R^2. The R^2 value for the right shoulder was the highest at 0.603, followed closely by the left shoulder with an R^2 value of 0.567. The R^2 value for all remaining variables was less than 0.3, indicating weak predictive power. The results of the present study were then compared to the four traditional macroscopic aging techniques: suture closure, morphology of the sternal rib ends, morphology of the auricular surface and the pubic symphysis. Sample distribution, correlation data, derived age ranges and error rates were compared between previous research and the results of the present study. All age estimation techniques demonstrated a positive correlation with age. Age ranges that were derived using Bayesian statistics or individual prediction intervals are more accurate at predicting actual age than those that were generated using confidence intervals of the mean, which provide information for mean age rather than actual age. In addition, the relationship between bone density and survivability of elements is discussed. It was determined that the skeletal elements utilized in traditional macroscopic aging are prone to breakage and loss based on their bone mineral density and location within the skeleton. In contrast, the proposed method utilized areas of the skeleton which are not typically examined for aging yet are likely to survive destruction from common taphonomic forces, making the use of OA in fragmentary or damaged contexts possible. Future research is needed to address the effects of ancestral variation and interobserver on the proposed method

Developmental regulation of GABAergic interneuron branching and synaptic development in the prefrontal cortex by soluble neural cell adhesion molecule

Neural cell adhesion molecule, NCAM, is an important regulator of neuronal process outgrowth and synaptic plasticity. Transgenic mice that overexpress the soluble NCAM extracellular domain (NCAM-EC) have reduced GABAergic inhibitory and excitatory synapses, and altered behavioral phenotypes. Here, we examined the role of dysregulated NCAM shedding, modeled by overexpression of NCAM-EC, on development of GABAergic basket interneurons in the prefrontal cortex. NCAM-EC overexpression disrupted arborization of basket cells during the major period of axon/dendrite growth, resulting in decreased numbers of GAD65- and synaptophysin-positive perisomatic synapses. NCAM-EC transgenic protein interfered with interneuron branching during early postnatal stages when endogenous polysialylated (PSA) NCAM was converted to non-PSA isoforms. In cortical neuron cultures, soluble NCAM-EC acted as a dominant inhibitor of NCAM-dependent neurite branching and outgrowth. These findings suggested that excess soluble NCAM-EC reduces perisomatic innervation of cortical neurons by perturbing axonal/dendritic branching during cortical development

Synthesis, Electrochemistry, and Excited-State Properties of Three Ru(II) Quaterpyridine Complexes

The complexes [Ru(qpy)LL′]2+ (qpy = 2,2′:6′,2″:6″,2‴-quaterpyridine), with 1: L = acetonitrile, L′= chloride; 2: L = L′= acetonitrile; and 3: L = L′= vinylpyridine, have been prepared from [Ru(qpy) (Cl)2]. Their absorption spectra in CH3CN exhibit broad metal-to-ligand charge transfer (MLCT) absorptions arising from overlapping 1A1 → 1MLCT transitions. Photoluminescence is not observed at room temperature, but all three are weakly emissive in 4:1 ethanol/methanol glasses at 77 K with broad, featureless emissions observed between 600 and 1000 nm consistent with MLCT phosphorescence. Cyclic voltammograms in CH3CN reveal the expected RuIII/II redox couples. In 0.1 M trifluoroacetic acid (TFA), 1 and 2 undergo aquation to give [RuII(qpy)(OH2)2]2+, as evidenced by the appearance of waves for the couples [RuIII(qpy)(OH2)2]3+/[RuII(qpy)(OH2)2]2+, [RuIV(qpy)(O)(OH2)]2+/[RuIII(qpy)(OH2)2]3+, and [RuVI(qpy)(O)2]2+/[RuIV(qpy)(O)(OH2)]2+ in cyclic voltammograms

Direct observation of light-driven, concerted electron–proton transfer

Concerted proton-coupled electron transfer (EPT) reactions in which both electrons and protons transfer in tandem are at the heart of many chemical and biological conversions including photosystem II. We report here the direct observation of absorption bands arising from photoEPT transitions, in this case, in H-bonded complexes between N-methyl-4,4′-bipyridinium cation and biologically relevant donors including tyrosine. The importance of these observations follows from the earlier experimental observations by Taube and coworkers on intervalence transfer in mixed-valence complexes. The observation of these photoEPT transitions and the appearance of reactive radical products also points to a possible, if inefficient, role in DNA photodamage and, possibly, in the formation of reactive oxygen intermediates

Fine tuning of MLCT states in new mononuclear complexes of ruthenium(II) containing tris(1-pyrazolyl)methane, 2,2′-bipyridine and aromatic nitrogen heterocycles

The syntheses of new mononuclear ruthenium(II) complexes of the type: [Ru(bpy)(L)(tpm)](PF6)2 {tpm = tris(1-pyrazolyl)-methane; bpy = 2,2′-bipyridine; L = pz (pyrazine; 1), 4,4′-bpy (4,4′-bipyridine; 2), and bpe [trans-1,2-bis(4-pyridyl)ethylene; 3]} are described, together with their spectroscopic, electrochemical, and photophysical properties. A complete assignment of the NMR resonances of the three species could be made in CD3CN by bidimensional techniques. A fine tuning of the energies of MLCT (metal-to-ligand charge transfer) states in these complexes is disclosed when comparing, in CH3CN, the values of their maximum absorption wave-lengths for the most intense visible bands (λ max) and their redox potentials for the RuIII/Ru II couples; this effect, relevant to the design of efficient photocatalysts, can be attributed to a decreasing order of dπ(Ru) →*(2,2′-bpy) backbonding when decreasing the distance between both N atoms in the aromatic nitrogen heterocycle L that acts in a monodentate manner. Only the species with L = bpe emits at room temperature, pointing to the conclusion that MLCT excited states in this series become higher in energy than dd excited states when the value of λmax is lower than 400 nm. These species are also useful building blocks for new dinuclear mixed-valent complexes. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.Fil: Katz, Néstor Eduardo. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaFil: Romero, Isabel. Universidad de Girona; EspañaFil: Llobet, Antoni. Universidad de Girona; EspañaFil: Parella, Teodor. Universitat Autònoma de Barcelona; EspañaFil: Benet Buchholz, Jordi. Bayer Industry Services; Alemani

Polysialylated NCAM and EphrinA/EphA regulate synaptic development of gabaergic interneurons in prefrontal cortex

A novel function for the neural cell adhesion molecule (NCAM) was identified in ephrinA/EphA-mediated repulsion as an important regulatory mechanism for development of GABAergic inhibitory synaptic connections in mouse prefrontal cortex. Deletion of NCAM, EphA3, or ephrinA2/3/5 in null mutant mice increased the numbers and size of perisomatic synapses between GABAergic basket interneurons and pyramidal cells in the developing cingulate cortex (layers II/III). A functional consequence of NCAM loss was increased amplitudes and faster kinetics of miniature inhibitory postsynaptic currents in NCAM null cingulate cortex. NCAM and EphA3 formed a molecular complex and colocalized with the inhibitory presynaptic marker vesicular GABA transporter (VGAT) in perisomatic puncta and neuropil in the cingulate cortex. EphrinA5 treatment promoted axon remodeling of enhanced green fluorescent protein-labeled basket interneurons in cortical slice cultures and induced growth cone collapse in wild-type but not NCAM null mutant neurons. NCAM modified with polysialic acid (PSA) was required to promote ephrinA5-induced axon remodeling of basket interneurons in cortical slices, likely by providing a permissive environment for ephrinA5/EphA3 signaling. These results reveal a new mechanism in which NCAM and ephrinAs/EphA3 coordinate to constrain GABAergic interneuronal arborization and perisomatic innervation, potentially contributing to excitatory/inhibitory balance in prefrontal cortical circuitry. © 2012 The Author

Tuning the photophysical properties of BODIPY dyes through extended aromatic pyrroles

A series of naphthyl and fluorantho-fused BODIPY dyes have been synthesized by a simple two-step process. These dyes display high molar absorptivities in the far visible region of the spectrum with emission quantum efficiencies at or near unity

Neural cell adhesion molecule, NCAM, regulates thalamocortical axon pathfinding and the organization of the cortical somatosensory representation in mouse

To study the potential role of neural cell adhesion molecule (NCAM) in the development of thalamocortical (TC) axon topography, wild type, and NCAM null mutant mice were analyzed for NCAM expression, projection, and targeting of TC afferents within the somatosensory area of the neocortex. Here we report that NCAM and its α-2,8-linked polysialic acid (PSA) are expressed in developing TC axons during projection to the neocortex. Pathfinding of TC axons in wild type and null mutant mice was mapped using anterograde DiI labeling. At embryonic day E16.5, null mutant mice displayed misguided TC axons in the dorsal telencephalon, but not in the ventral telencephalon, an intermediate target that initially sorts TC axons toward correct neocortical areas. During the early postnatal period, rostrolateral TC axons within the internal capsule along the ventral telencephalon adopted distorted trajectories in the ventral telencephalon and failed to reach the neocortex in NCAM null mutant animals. NCAM null mutants showed abnormal segregation of layer IV barrels in a restricted portion of the somatosensory cortex. As shown by Nissl and cytochrome oxidase staining, barrels of the anterolateral barrel subfield (ALBSF) and the most distal barrels of the posteromedial barrel subfield (PMBSF) did not segregate properly in null mutant mice. These results indicate a novel role for NCAM in axonal pathfinding and topographic sorting of TC axons, which may be important for the function of specific territories of sensory representation in the somatosensory cortex

Sensitization of ultra-long-range excited-state electron transfer by energy transfer in a polymerized film

Distance-dependent energy transfer occurs from the Metal-to-Ligand Charge Transfer (MLCT) excited state to an anthracene-acrylate derivative (Acr-An) incorporated into the polymer network of a semirigid poly(ethyleneglycol)dimethacrylate monolith. Following excitation, to Acr-An triplet energy transfer occurs followed by long-range, Acr-3An—Acr-An → Acr-An—Acr-3An, energy migration. With methyl viologen dication (MV2+) added as a trap, Acr-3An + MV2+ → Acr-An+ + MV+ electron transfer results in sensitized electron transfer quenching over a distance of approximately 90 Å