The resulting supernatant was resuspended in 10 μL of Solution A. The protein concentration of the nuclear and mitochondria/cytoplasm fractions was determined using the Biorad Protein Assay. These procedures were done as previously described 20. Quantitation of the Western blots was performed using Adobe Photoshop CS3 as described (http://lukemiller.org/journal/2007/08/quantifying-western-blots-without.html).

Briefly, the Adobe Photoshop lasso tool was used to outline each protein band and a background region on the membrane. The mean gray value and the pixel value were multiplied to determine the absolute intensity of the band. When no band was visible, the outlined region was made equal in pixel number to that of the JQ1 order background region. The background to be subtracted from a given band was determined by multiplying the mean gray value of the outlined background region by the pixel

measurement for the corresponding band. The authors thank Victor E. Marquez for his generous gift of HK434 and Yuefang Sun for taking care of the mouse colonies. BIBW2992 nmr This study was supported by a grant from the National Institute of Health (to A. W.) and the Research Supplement for underrepresented minorities from the National Cancer Institute (to J. T.). Conflict of interest: The authors Selleck Gefitinib declare no financial or commercial conflict of interest. “
“Monocytes are blood leukocytes that can differentiate into several phagocytic cell types, including DCs, which are instrumental to the inflammatory response and host defence against

microbes. A study published in this issue of the European Journal of Immunology by Balboa et al. [Eur. J. Immunol. 2013. 43: 335-347] suggests that a shift of the CD16− monocyte population toward a CD16+ subpopulation may represent an immune evasion strategy that ultimately favors persistence of Mycobacterium tuberculosis. Together with other recent reports, the article by Balboa et al. sheds new light on the function of CD16+ monocytes in health and disease; in this commentary, we discuss the implications stemming from these findings. Immunity to pathogens and inflammatory reactions relies on the coordinated action of several immune cell populations including lymphoid cells and monocyte-derived phagocytes, such as macrophages and DCs. Monocytes are generated in the marrow and circulate in the blood where they can patrol the whole body for signs of infection or inflammation, and migrate to injured tissues upon attraction by several chemokines and microbial ligands. Monocytes exhibit high plasticity and can differentiate into a variety of cell subsets depending on their microenvironment in infected or inflamed tissues [1, 2].