(c) 2012 Wiley Periodicals, Inc. Dev Psychobiol 56: 73-85, 2014.”
“High temperature affects numerous biochemical and physiological traits in plants. Primary leaves of sunflower (Helianthus annuus L.) were collected from plants grown under a control temperature (day/night regime of 23/19 degrees C) or a high temperature (day/night regime of 33/29 degrees C) for 16, 22, 28, 32 or 42 d. Leaves of sunflower BMS-777607 mouse plants exposed to high temperature

exhibited decreased growth, as reflected by lower specific leaf mass and reduced leaf area as compared with controls. A superior decrease in soluble protein content during leaf life span in plants grown at high temperature relative to control plants (70% vs. 45%, respectively) suggests that high temperature promotes soluble protein degradation in leaves. High temperature also reduces net photosynthetic rate (P-N) possibly by decreasing the content in photosynthetic pigments and the stomatal conductance (g(s)). The activity of nitrate reductase and glutamine synthetase decreased while deaminating activity in glutamate dehydrogenase increased in leaves exposed to high temperature. Our results suggest selleck products that high temperature induced early senescence in sunflower leaves, probably as a result of an accumulation of soluble sugars and the associated decrease in starch levels. Oxidative damage resulting from increased H2O2

accumulation and a decline in antioxidant activity may have also contributed to accelerated senescence of primary leaves at high temperature.”
“Stem and progenitor cells maintain the tissue they reside in for life by regulating the balance between proliferation and differentiation. How this is done is not well understood. Here, we report that the human exosome maintains progenitor cell function. The expression of several subunits of the exosome were found to be enriched in epidermal progenitor cells, which were required to retain

proliferative capacity and to prevent premature differentiation. Loss of PM/Scl-75 also known this website as EXOSC9, a key subunit of the exosome complex, resulted in loss of cells from the progenitor cell compartment, premature differentiation, and loss of epidermal tissue. EXOSC9 promotes self-renewal and prevents premature differentiation by maintaining transcript levels of a transcription factor necessary for epidermal differentiation, GRHL3, at low levels through mRNA degradation. These data demonstrate that control of differentiation specific transcription factors through mRNA degradation is required for progenitor cell maintenance in mammalian tissue.”
“Background Vaccination with hypoallergenic recombinant Bet v 1 derivatives (Bet v 1 fragments and Bet v 1 trimer) is associated with the induction of IgG antibodies specific to natural Bet v 1.