Journal: Life Science Alliance

Article Title: Redundant and nonredundant organismal functions of EPS15 and EPS15L1

doi: 10.26508/lsa.201800273

Figure Lengend Snippet: (A) Methylene blue–stained blood smears of adult WT mice, 7 d after injection with PBS or PHZ. Note numerous blue dye–retaining reticulocytes in the blood smear from PHZ-treated mice. Bar, 10 μm. (B) FACS analysis with anti-TfR/CD71 and thiazole orange to analyze the maturation status of RBCs from WT mice at 0, 7, 10, and 16 d after PHZ injection. (C) Western blotting of blood lysates at 7, 10, and 16 d after treatment with PHZ. Equal amounts of lysates, corresponding to 7 μl of whole blood, were loaded and probed for the indicated proteins. (D) Western blotting of brain (Br), liver (Li), and spleen (Sp) lysates from adult WT and cDKO mice. Twenty micrograms of each lysate was loaded. (E) Iron, transferrin, and ferritin levels in the serum of adult WT and cDKO mice. Three animals of each phenotype were analyzed. ** P < 0.01 versus WT. Note that the iron levels were increased in the serum of cDKO mice, indicating that iron absorption was not defective. (F) Perls’ Prussian blue staining of the liver and spleen of adult WT and cDKO mice. Iron deposition is in blue. Arrows point to increased erythropoiesis in the spleen of cDKO mice. Bar, 50 μm. Note that, despite increased serum iron, we did not detect tissue iron overload in the spleen or liver of cDKO mice. In contrast, other murine models of microcytic hypochromic anemia, such as the hematopoietic-specific KO for Stat5a/b , present iron overload in the liver . A possible explanation might be that cDKO displayed increased secondary erythropoiesis, particularly in the spleen (this panel), which actively remove iron excess. Consistent with the absence of tissue iron overload, other iron metabolism proteins (transferrin and ferritin) were not altered in cDKO mice (panel E), indicating that a certain balance in iron metabolism in cDKO mice has still been preserved and/or re-established. (G) Molecular phylogenesis of the EPS15 family. Protein sequences were retrieved from the NCBI or the Joint Genome Institute ( http://genome.jgi.doe.gov/ ) databases. Sequences were aligned with ClustalW, and the evolutionary history was inferred by using the maximum likelihood method based on the JTT matrix–based model . The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. All positions containing gaps and missing data were eliminated. Alignment and evolutionary analyses were conducted in MEGA7 . Protein accession numbers are shown.

Article Snippet: Staining was performed using Perls' Prussian blue stain kit (DDK Italia), according to the manufacturer's instructions.

Techniques: Staining, Injection, Western Blot