The Influence of Oxygen Fugacity and Cooling Rate on the Crystallization of Ca-Al Inclusions from Allende

Although there appears to be general agreement that some coarse-grained Ca-Al-rich inclusions (CAIs) from Allende passed through a molten or partially molten stage in their evolution, there are several competing hypotheses to account for the formation of the liquid phase in CAIs (e.g., 1-4). Studies of the phase equilibria of CAI compositions can help distinguish between these mechanisms for generating liquids in CAIs

Arsenite-Induced Alterations of DNA Photodamage Repair and Apoptosis After Solar-Simulation UVR in Mouse Keratinocytes in Vitro

Our laboratory has shown that arsenite markedly increased the cancer rate caused by solar-simulation ultraviolet radiation (UVR) in the hairless mouse skin model. In the present study, we investigated how arsenite affected DNA photodamage repair and apoptosis after solar-simulation UVR in the mouse keratinocyte cell line 291.03C. The keratinocytes were treated with different concentrations of sodium arsenite (0.0, 2.5, 5.0 μM) for 24 hr and then were immediately irradiated with a single dose of 0.30 kJ/m(2) UVR. At 24 hr after UVR, DNA photoproducts [cyclobutane pyrimidine dimers (CPDs) and 6–4 photoproducts (6-4PPs)] and apoptosis were measured using the enzyme-linked immunosorbent assay and the two-color TUNEL (terminal deoxynucleotide transferase dUTP nick end labeling) assay, respectively. The results showed that arsenite reduced the repair rate of 6-4PPs by about a factor of 2 at 5.0 μM and had no effect at 2.5 μM. UVR-induced apoptosis at 24 hr was decreased by 22.64% at 2.5 μM arsenite and by 61.90% at 5.0 μM arsenite. Arsenite decreased the UVR-induced caspase-3/7 activity in parallel with the inhibition of apoptosis. Colony survival assays of the 291.03C cells demonstrate a median lethal concentration (LC(50)) of arsenite of 0.9 μM and a median lethal dose (LD(50)) of UVR of 0.05 kJ/m(2). If the present results are applicable in vivo, inhibition of UVR-induced apoptosis may contribute to arsenite’s enhancement of UVR-induced skin carcinogenesis

Allendeite and Hexamolybdenum: Two New Ultra-Refractory Minerals in Allende and Two Missing Links

During our nano-mineralogy investigation of the Allende meteorite, we discovered two new minerals that occur as micro- to nano-crystals in refractory inclusions: Allendeite, Sc_4Zr_3O_(12), a new Scand Zr-rich oxide; and hexamolybdenum, (Mo,Ru,Fe), a Mo-dominant alloy. Allendeite, which may be an important ultra-refractory carrier linking Zr-, Sc- oxides and the more common Sc-, Zr-enriched clinopyroxenes (Cpx) in CAIs, hosts perovskite (Pv), spinel (Sp), Os-Ir-W-Mo alloys, and hexamolybdenum. The observation of two structurally and chemically distinct highly refractory, low-Pt alloy minerals not associated with Fe-Ni alloys provides the first direct physical evidence for at least two separate carriers of the highly refractory metals in CAIs. Hexamolybdenum links Osrich and Pt-rich meteoritic alloys and may be a precursor of the latter. Both new minerals have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA 2007-027, 029)

Morphological, Structural, and Spectral Characteristics of Amorphous Iron Sulfates

Current or past brine hydrologic activity on Mars may provide suitable conditions for the formation of amorphous ferric sulfates. Once formed, these phases would likely be stable under current Martian conditions, particularly at low- to mid-latitudes. Therefore, we consider amorphous iron sulfates (AIS) as possible components of Martian surface materials. Laboratory AIS were created through multiple synthesis routes and characterized with total X-ray scattering, thermogravimetric analysis, scanning electron microscopy, visible/near-infrared (VNIR), thermal infrared (TIR), and Mössbauer techniques. We synthesized amorphous ferric sulfates (Fe(III)2(SO4)3 · ~ 6–8H2O) from sulfate-saturated fluids via vacuum dehydration or exposure to low relative humidity

RAS isoforms and mutations in cancer at a glance

RAS proteins (KRAS4A, KRAS4B, NRAS and HRAS) function as GDP–GTP-regulated binary on-off switches, which regulate cytoplasmic signaling networks that control diverse normal cellular processes. Gain-of-function missense mutations in RAS genes are found in ∼25% of human cancers, prompting interest in identifying anti-RAS therapeutic strategies for cancer treatment. However, despite more than three decades of intense effort, no anti-RAS therapies have reached clinical application. Contributing to this failure has been an underestimation of the complexities of RAS. First, there is now appreciation that the four human RAS proteins are not functionally identical. Second, with >130 different missense mutations found in cancer, there is an emerging view that there are mutation-specific consequences on RAS structure, biochemistry and biology, and mutation-selective therapeutic strategies are needed. In this Cell Science at a Glance article and accompanying poster, we provide a snapshot of the differences between RAS isoforms and mutations, as well as the current status of anti-RAS drug-discovery efforts

Shear waves induced by moving needle in MR Elastography

Magnetic Resonance Elastography (MRE) is a phase contrast-based method for observing shear wave propagation in a material to determine its stiffness. The objective of this study was to determine whether shear waves suitable for MRE can be induced using a moving acupuncture needle. Tissue-simulating bovine gel phantom and a 0.4mm diameter acupuncture needle were used in the experiment. The results showed that observable shear waves could be induced in the gel phantom by cyclic needle motion. The observed wavelength varied with excitation frequency, as expected. Generating shear waves using moving needles may be a useful tool to study the basic mechanism of acupuncture with MRE. Further study will be conducted to observe the wave motion in inhomogeneous media and acupuncture-induced effects in invivo studies.published_or_final_versio