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10.1007/PL00000811 http://scihub22266oqcxt.onion/10.1007/PL00000811 11706999!ä!11706999 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Cell+Mol+Life+Sci 2001 ; 58 (11): 1727-33 Nephropedia Template TP {{tp|p=11706999|t=2001. Role of serum components in the binding and phagocytosis of oxidatively damaged erythrocytes by autologous mouse macrophages |pdf=|usr=}}{{11706999}} gab.com Text Role of serum components in the binding and phagocytosis of oxidatively damaged erythrocytes by autologous mouse macrophages JO: Cell Mol Life Sci http://www.kidney.de/pget.php?&tw=1&pmid=11706999 #FOAvip To investigate the role of autologous serum components in the recognition of damaged cells by macrophages, we examined the binding and phagocytosis of damage oxidatively damaged red blood cells with Cu2+ and ascorbate (oxRBCs) by autologous resident mouse peritoneal macrophages. The binding of oxRBCs by macrophages was independent of the presence of serum. However, phagocytosis by macrophages increased with serum concentration, and macrophages showed little ingestion of oxRBCs in a serum-free medium. Macrophages neither bound nor appreciably ingested native RBCs (before oxidation) in either the absence or presence of autologous serum. Mouse macrophages ingested significantly more native as well as oxRBCs in the presence of heat-inactivated fetal calf serum than in the presence of heat-inactivated mouse serum. Pretreated oxRBCs with normal serum were rarely ingested by macrophages in a serum-free medium. Phagocytosis of oxRBCs was significantly inhibited by depletion of IgG or calcium from serum, by heat inactivation of complement, or by antiserum against mouse C3. These results demonstrate that serum components such as IgG, C3, and calcium are involved in phagocytosis of oxRBCs by autologous macrophages. Twit Text FOAVip Role of serum components in the binding and phagocytosis of oxidatively damaged erythrocytes by autologous mouse macrophages ????Cell Mol Life Sci http://www.kidney.de/pget.php?&tw=1&pmid=11706999 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=11706999 #FOAvip English Wikipedia <ref>{{Cite pmid|11706999}}</ref> Role of serum components in the binding and phagocytosis of oxidatively damaged erythrocytes by autologous mouse macrophages #MMPMID11706999 Tanaka K; Usui Y; Kojo S Cell Mol Life Sci 2001[Oct]; 58 (11): 1727-33 PMID11706999show ga To investigate the role of autologous serum components in the recognition of damaged cells by macrophages, we examined the binding and phagocytosis of damage oxidatively damaged red blood cells with Cu2+ and ascorbate (oxRBCs) by autologous resident mouse peritoneal macrophages. The binding of oxRBCs by macrophages was independent of the presence of serum. However, phagocytosis by macrophages increased with serum concentration, and macrophages showed little ingestion of oxRBCs in a serum-free medium. Macrophages neither bound nor appreciably ingested native RBCs (before oxidation) in either the absence or presence of autologous serum. Mouse macrophages ingested significantly more native as well as oxRBCs in the presence of heat-inactivated fetal calf serum than in the presence of heat-inactivated mouse serum. Pretreated oxRBCs with normal serum were rarely ingested by macrophages in a serum-free medium. Phagocytosis of oxRBCs was significantly inhibited by depletion of IgG or calcium from serum, by heat inactivation of complement, or by antiserum against mouse C3. These results demonstrate that serum components such as IgG, C3, and calcium are involved in phagocytosis of oxRBCs by autologous macrophages. |Animals[MESH] |Calcium/blood[MESH] |Complement C3/chemistry/metabolism[MESH] |Erythrocytes/*metabolism/pathology[MESH] |Immunoglobulin G/blood[MESH] |Macrophages, Peritoneal/*metabolism[MESH] |Magnesium/metabolism[MESH] |Mice[MESH] |Oxidation-Reduction[MESH]Role of serum components in the binding and phagocytosis of oxidativel(epmc).pdf DeepDyve Pubget Overpricing