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Mapping Asia Plants (MAP) is a comprehensive project that aims to build a detailed infrastructure for integrating Asian plant distribution data a global-scale array of knowledge for plant biodiversity conservation. Here, we provide a brief historical review of botanical research in Southwest Asia – an understudied botanical region with high conservation priority. Nineteen countries were included in this study (from west to east): Turkey, Cyprus, Palestine, Israel, Jordan, Saudi Arabia, Lebanon, Syria, Iraq, Georgia, Yemen, Armenia, Iran, Azerbaijan, Kuwait, Bahrain, Qatar, United Arab Emirates, and Oman. We reviewed 132 resources comprising 125 Floras and Checklists, of which we describe in some detail at least one of the most important Floras or Checklists for each country. Complete and published national Floras exist for 13 countries; three countries (Jordan, Israel and Bahrain) do not have a Flora but have annotated Checklists, and national Floras are at different stages of completion for Iran, Iraq and Georgia. Where present, online resources are also given for references. We found major gaps in species concepts and taxonomic classification systems, and that many up-to-date Flora revisions remained unresolved, i.e. taxon ranks and species concepts varied among different countries, different systems were adopted or followed in the taxonomic treatments in the Floras and Checklists, and some of the current Floras are out of date. Floras are the first necessary step for many fields, including evolutionary biology, ecology, biogeography, and systematics, as well as environmental research and conservation of biodiversity at national and international levels. Here, we provide the progress updates on the main published floristic works of Southwest Asia, which continue to serve as references for the Flora of Southwest Asia, and will be the foundation of the MAP project.

Macrophage accumulation within the vascular wall is a hallmark of atherosclerosis. Controlling macrophage conversion into foam cells remains a major challenge for treatment of atherosclerotic diseases. Here, we show that Wip1, a member of the PP2C family of Ser/Thr protein phosphatases, modulates macrophage migration and phagocytosis associated with atherosclerotic plaque formation. Wip1 deficiency increases migratory and phagocytic activities of the macrophage under stress conditions. Enhanced migration of Wip1-/- macrophages is mediated by Rac1-GTPase and PI3K/AKT signalling pathways. Elevated phagocytic ability of Wip1-/- macrophages is linked to CD36 plasma membrane recruitment that is regulated by AMPK activity. Our study identifies Wip1 as an intrinsic negative regulator of macrophage chemotaxis. We propose that Wip1-dependent control of macrophage function may provide avenues for preventing or eliminating plaque formation in atherosclerosis.

Background: Calcium phosphate mediated transfection has been used for delivering DNA into mammalian cells in excess of 30 years due to its most low cost for introducing recombinant DNA into culture cells. However, multiple factors affecting the transfect efficiency are commonly recognized meanwhile for years, the low transfection efficiency of this approach on higher differentiated and non-tumor cells such as CHO and C2C12 limits its application on research. Results: In this paper, we systematically evaluated the possible factors affecting the transfection rate of this approach. Two categories, calcium phosphate–DNA co-precipitation and on-cell treatments were set for optimization of plasmid DNA transfection into CHO and C2C12 cell-lines. Throughout experimentation of these categories such as buffer system, transfection media and time, glycerol shocking and so on, we optimized the best procedure to obtain the highest efficiency ultimately. During calcium phosphate DNA-precipitation, the transfection buffer is critical condition optimized with HBS at pH 7.10 (P = 0.013 compared to HEPES in CHO). In the transfection step, FBS is a necessary component in transfection DMEM for high efficiency (P = 0.0005 compared to DMEM alone), and high concentration of co-precipitated particles applied to cultured cells in combination with intermittent vortexing is also crucial to preserve the efficiency. For 6-well culture plates, 800 µl of co-precipitated particles (11.25 µg/mL of cDNA) in 1 well is the optimal (P = 0.007 compared to 200 µl). For the highest transfection efficiency, the most important condition is glycerol in shock treatment (P = 0.002 compared to no shock treatment in CHO, and P = 0.008 compared to no shock treatment in C2C12) after a 6 h incubation (P = 0.004 compared to 16 h in CHO, and P = 0.039 compared to 16 h in C2C12) on cultured cells. Conclusions: Calcium phosphate mediated transfection is the most low-cost approach to introduce recombinant DNA into culture cells. However, the utility of this procedure is limited in highly-differentiated cells. Here we describe the specific HBS-buffered saline, PH, glycerol shock, vortex strength, transfection medium, and particle concentrations conditions necessary to optimize this transfection method in highly differentiated cells.