Slc40a1 macrophage
WebApr 1, 2013 · Intestinal iron absorption is mediated by SLC11A2 at the apical membrane of enterocytes, followed by basolateral exit via SLC40A1. To meet the daily requirement for iron, approximately 80% of the iron comes from the breakdown of hemoglobin following macrophage phagocytosis of senescent erythrocytes (iron recycling). WebThe SLC40A1 gene encodes ferroportin, a protein responsible for exporting iron from cells in the intestine, liver, spleen, and kidney, as well as from reticuloendothelial macrophages and the placenta. [6] [7] More than 39 mutations to the SLC40A1 gene have been identified in patients with type 4 hemochromatosis. [7]
Slc40a1 macrophage
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WebAug 13, 2024 · M2 macrophages, which resemble tumor-associated macrophages, express iron-efflux genes with increased SLC40A1 and decreased ferritin . When cultured with … WebOct 31, 2024 · Of the macrophages in tumors that exhibited distinct transcriptional states, tumor-associated macrophages (TAMs) were associated with poor prognosis, and we …
WebSep 13, 2024 · First, a population of liver capsule macrophages (LCMs) have been identified ( Sierro et al., 2024 ). The liver capsule consists of a single layer of mesothelial cells and a single stratum of capsular fibroblasts existing just beneath the … WebMay 17, 2024 · We also revealed that a subset of macrophages expressing SLC40A1 and genes reacting to various infections was present in para-carcinoma but not in HCC tissue. These findings were independently validated with scRNA-Seq and large-scale tissue bulk RNA-Seq/microarray analyses.
WebNatural resistance-associated macrophage protein 1 is a protein that in humans is encoded by the SLC11A1 gene. Function. This gene is a member of the solute carrier family 11 (proton-coupled divalent metal ion transporters) family and encodes a multi-pass membrane protein. The protein functions as a divalent transition metal (iron and manganese ... WebIron overloading disorders linked to mutations in ferroportin have diverse phenotypes in vivo, and the effects of mutations on ferroportin in vitro range from loss of function (LOF) to gain of function (GOF) with hepcidin resistance. We reviewed 359 patients with 60 ferroportin variants. Overall, macrophage iron overload and low/normal transferrin saturation (TSAT) …
WebJun 16, 2024 · Tissue-resident macrophages accumulate close to tumour cells early during tumour formation to promote epithelial–mesenchymal transition and invasiveness in tumour cells, and they also induce a...
WebFerroportin (SLC40A1) is an iron transporter postulated to play roles in intestinal iron absorption and cellular iron release. Hepcidin, a regulatory peptide, binds to ferroportin … my playce family fun room marlow heights mdWebJul 18, 2016 · At 16 h, a population of CD11b high F4/80 high macrophages (henceforth called transient macrophages (tMΦs)) appeared in the liver , but the number of F4/80 high CD11b int KCs was diminished. my play town freeWebFeb 7, 2024 · SLC40A1 solute carrier family 40 member 1. SLC40A1. solute carrier family 40 member 1. Gene ID: 30061, updated on 7-Feb-2024. Gene type: protein coding. Also … my play venusWebThe SLC40A1 gene is associated with autosomal dominant ferroportin disease (aka hemochromatosis type 4 (HFE4)) (MedGen UID: 340044). Providers. Providers Home. … my play worldWebSLC40A1. gene product. FPN1, HFE4, IREG1, MTP1, SLC11A3. The protein encoded by this gene is a cell membrane protein that may be involved in iron export from duodenal … my play school cd learnware image sWebMar 9, 2024 · Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 [ (house mouse)] Gene ID: 53945, updated on 9-Mar-2024. Summary. Enables ferrous iron … my playbackWebMar 10, 2011 · A patient heterozygous for the variant p.W158C in SLC40A1 presented with macrophage iron overload, hyperferritinemia, and normal transferrin saturation. A patient with hepatocellular iron storage, hyperferritinemia, and increased transferrin saturation was heterozygous for p.H507R. my player 2