메뉴 건너뛰기




Volumn 175, Issue 4, 2016, Pages 714-723

Sustained treatment of sickle cell mice with haptoglobin increases HO-1 and H-ferritin expression and decreases iron deposition in the kidney without improvement in kidney function

Author keywords

free haemoglobin; H ferritin; haem oxygenase 1; haptoglobin; sickle cell disease

Indexed keywords

FERRITIN; HAPTOGLOBIN; HEAVY CHAIN FERRITIN; HEME OXYGENASE 1; UNCLASSIFIED DRUG; APOFERRITIN; IRON;

EID: 84983000268     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/bjh.14280     Document Type: Article
Times cited : (16)

References (59)
  • 1
    • 84961025829 scopus 로고
    • The binding of haemoglobin by plasma proteins (haptoglobins); its bearing on the renal threshold for haemoglobin and the aetiology of haemoglobinuria
    • Allison, A.C. & Rees, W.A. (1957) The binding of haemoglobin by plasma proteins (haptoglobins); its bearing on the renal threshold for haemoglobin and the aetiology of haemoglobinuria. British Medical Journal, 2, 1137–1143.
    • (1957) British Medical Journal , vol.2 , pp. 1137-1143
    • Allison, A.C.1    Rees, W.A.2
  • 2
    • 0028828562 scopus 로고
    • Heme degradation in the presence of glutathione. A proposed mechanism to account for the high levels of non-heme iron found in the membranes of hemoglobinopathic red blood cells
    • Atamna, H. & Ginsburg, H. (1995) Heme degradation in the presence of glutathione. A proposed mechanism to account for the high levels of non-heme iron found in the membranes of hemoglobinopathic red blood cells. Journal of Biological Chemistry, 270, 24876–24883.
    • (1995) Journal of Biological Chemistry , vol.270 , pp. 24876-24883
    • Atamna, H.1    Ginsburg, H.2
  • 4
    • 0037072443 scopus 로고    scopus 로고
    • Soluble adhesion molecules and the search for biomarkers for atherosclerosis
    • Ballantyne, C.M. & Entman, M.L. (2002) Soluble adhesion molecules and the search for biomarkers for atherosclerosis. Circulation, 106, 766–767.
    • (2002) Circulation , vol.106 , pp. 766-767
    • Ballantyne, C.M.1    Entman, M.L.2
  • 5
    • 1842539298 scopus 로고    scopus 로고
    • Haptoglobin phenotypes differ in their ability to inhibit heme transfer from hemoglobin to LDL
    • Bamm, V.V., Tsemakhovich, V.A., Shaklai, M. & Shaklai, N. (2004) Haptoglobin phenotypes differ in their ability to inhibit heme transfer from hemoglobin to LDL. Biochemistry, 43, 3899–3906.
    • (2004) Biochemistry , vol.43 , pp. 3899-3906
    • Bamm, V.V.1    Tsemakhovich, V.A.2    Shaklai, M.3    Shaklai, N.4
  • 9
    • 84888260688 scopus 로고    scopus 로고
    • MP4CO, a pegylated hemoglobin saturated with carbon monoxide is a modulator of HO-1, inflammation and vaso-occlusion in transgenic sickle mice
    • Belcher, J.D., Young, M., Chen, C., Nguyen, J., Burhop, K., Tran, P. & Vercellotti, G.M. (2013) MP4CO, a pegylated hemoglobin saturated with carbon monoxide is a modulator of HO-1, inflammation and vaso-occlusion in transgenic sickle mice. Blood, 122, 2757–64.
    • (2013) Blood , vol.122 , pp. 2757-2764
    • Belcher, J.D.1    Young, M.2    Chen, C.3    Nguyen, J.4    Burhop, K.5    Tran, P.6    Vercellotti, G.M.7
  • 15
    • 77949507541 scopus 로고    scopus 로고
    • Vacuolar ATPase regulates surfactant secretion in rat alveolar type II cells by modulating lamellar body calcium
    • Chintagari, N.R., Mishra, A., Su, L., Wang, Y., Ayalew, S., Hartson, S.D. & Liu, L. (2010) Vacuolar ATPase regulates surfactant secretion in rat alveolar type II cells by modulating lamellar body calcium. PLoS ONE, 5, e9228.
    • (2010) PLoS ONE , vol.5
    • Chintagari, N.R.1    Mishra, A.2    Su, L.3    Wang, Y.4    Ayalew, S.5    Hartson, S.D.6    Liu, L.7
  • 16
    • 84924002582 scopus 로고    scopus 로고
    • Haptoglobin attenuates hemoglobin-induced heme oxygenase-1 in renal proximal tubule cells and kidneys of a mouse model of sickle cell disease
    • Chintagari, N.R., Nguyen, J., Belcher, J.D., Vercellotti, G.M. & Alayash, A.I. (2015) Haptoglobin attenuates hemoglobin-induced heme oxygenase-1 in renal proximal tubule cells and kidneys of a mouse model of sickle cell disease. Blood Cells, Molecules, & Diseases, 54, 302–306.
    • (2015) Blood Cells, Molecules, & Diseases , vol.54 , pp. 302-306
    • Chintagari, N.R.1    Nguyen, J.2    Belcher, J.D.3    Vercellotti, G.M.4    Alayash, A.I.5
  • 17
    • 84946195292 scopus 로고    scopus 로고
    • Different target specificities of haptoglobin and hemopexin define a sequential protection system against vascular hemoglobin toxicity
    • Deuel, J.W., Vallelian, F., Schaer, C.A., Puglia, M., Buehler, P.W. & Schaer, D.J. (2015) Different target specificities of haptoglobin and hemopexin define a sequential protection system against vascular hemoglobin toxicity. Free Radical Biology and Medicine, 89, 931–943.
    • (2015) Free Radical Biology and Medicine , vol.89 , pp. 931-943
    • Deuel, J.W.1    Vallelian, F.2    Schaer, C.A.3    Puglia, M.4    Buehler, P.W.5    Schaer, D.J.6
  • 18
    • 84876902880 scopus 로고    scopus 로고
    • CD163 and inflammation: biological, diagnostic, and therapeutic aspects
    • Etzerodt, A. & Moestrup, S.K. (2013) CD163 and inflammation: biological, diagnostic, and therapeutic aspects. Antioxidants & Redox Signaling, 18, 2352–2363.
    • (2013) Antioxidants & Redox Signaling , vol.18 , pp. 2352-2363
    • Etzerodt, A.1    Moestrup, S.K.2
  • 23
    • 23944484733 scopus 로고    scopus 로고
    • An improved colorimetric method for quantitation of heme using tetramethylbenzidine as substrate
    • Huy, N.T., Xuan Trang, D.T., Uyen, D.T., Sasai, M., Harada, S. & Kamei, K. (2005) An improved colorimetric method for quantitation of heme using tetramethylbenzidine as substrate. Analytical Biochemistry, 344, 289–291.
    • (2005) Analytical Biochemistry , vol.344 , pp. 289-291
    • Huy, N.T.1    Xuan Trang, D.T.2    Uyen, D.T.3    Sasai, M.4    Harada, S.5    Kamei, K.6
  • 24
    • 0019223024 scopus 로고
    • Interaction between hemoglobin subunits in the hemoglobin. haptoglobin complex
    • Hwang, P.K. & Greer, J. (1980) Interaction between hemoglobin subunits in the hemoglobin. haptoglobin complex. Journal of Biological Chemistry, 255, 3038–3041.
    • (1980) Journal of Biological Chemistry , vol.255 , pp. 3038-3041
    • Hwang, P.K.1    Greer, J.2
  • 25
    • 84924225251 scopus 로고    scopus 로고
    • Hemoglobin-induced lung vascular oxidation, inflammation, and remodeling contribute to the progression of hypoxic pulmonary hypertension and is attenuated in rats with repeated-dose haptoglobin administration
    • Irwin, D.C., Baek, J.H., Hassell, K., Nuss, R., Eigenberger, P., Lisk, C., Loomis, Z., Maltzahn, J., Stenmark, K.R., Nozik-Grayck, E. & Buehler, P.W. (2015) Hemoglobin-induced lung vascular oxidation, inflammation, and remodeling contribute to the progression of hypoxic pulmonary hypertension and is attenuated in rats with repeated-dose haptoglobin administration. Free Radical Biology and Medicine, 82, 50–62.
    • (2015) Free Radical Biology and Medicine , vol.82 , pp. 50-62
    • Irwin, D.C.1    Baek, J.H.2    Hassell, K.3    Nuss, R.4    Eigenberger, P.5    Lisk, C.6    Loomis, Z.7    Maltzahn, J.8    Stenmark, K.R.9    Nozik-Grayck, E.10    Buehler, P.W.11
  • 26
    • 27244435213 scopus 로고    scopus 로고
    • Levels of soluble endothelium-derived adhesion molecules in patients with sickle cell disease are associated with pulmonary hypertension, organ dysfunction, and mortality
    • Kato, G.J., Martyr, S., Blackwelder, W.C., Nichols, J.S., Coles, W.A., Hunter, L.A., Brennan, M.L., Hazen, S.L. & Gladwin, M.T. (2005) Levels of soluble endothelium-derived adhesion molecules in patients with sickle cell disease are associated with pulmonary hypertension, organ dysfunction, and mortality. British Journal of Haematology, 130, 943–953.
    • (2005) British Journal of Haematology , vol.130 , pp. 943-953
    • Kato, G.J.1    Martyr, S.2    Blackwelder, W.C.3    Nichols, J.S.4    Coles, W.A.5    Hunter, L.A.6    Brennan, M.L.7    Hazen, S.L.8    Gladwin, M.T.9
  • 31
    • 84878741762 scopus 로고    scopus 로고
    • Human hp1-1 and hp2-2 phenotype-specific haptoglobin therapeutics are both effective in vitro and in Guinea pigs to attenuate hemoglobin toxicity
    • Lipiski, M., Deuel, J.W., Baek, J.H., Engelsberger, W.R., Buehler, P.W. & Schaer, D.J. (2013) Human hp1-1 and hp2-2 phenotype-specific haptoglobin therapeutics are both effective in vitro and in Guinea pigs to attenuate hemoglobin toxicity. Antioxidants & Redox Signaling, 19, 1619–1633.
    • (2013) Antioxidants & Redox Signaling , vol.19 , pp. 1619-1633
    • Lipiski, M.1    Deuel, J.W.2    Baek, J.H.3    Engelsberger, W.R.4    Buehler, P.W.5    Schaer, D.J.6
  • 32
    • 32644437616 scopus 로고    scopus 로고
    • Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell disease
    • Manci, E.A., Hillery, C.A., Bodian, C.A., Zhang, Z.G., Lutty, G.A. & Coller, B.S. (2006) Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell disease. Blood, 107, 1651–1658.
    • (2006) Blood , vol.107 , pp. 1651-1658
    • Manci, E.A.1    Hillery, C.A.2    Bodian, C.A.3    Zhang, Z.G.4    Lutty, G.A.5    Coller, B.S.6
  • 33
    • 74849088905 scopus 로고    scopus 로고
    • Urine concentrating ability in infants with sickle cell disease: baseline data from the phase III trial of hydroxyurea (BABY HUG)
    • Miller, S.T., Wang, W.C., Iyer, R., Rana, S., Lane, P., Ware, R.E., Li, D., Rees, R.C. & Investigators, B.-H. (2010) Urine concentrating ability in infants with sickle cell disease: baseline data from the phase III trial of hydroxyurea (BABY HUG). Pediatric Blood & Cancer, 54, 265–268.
    • (2010) Pediatric Blood & Cancer , vol.54 , pp. 265-268
    • Miller, S.T.1    Wang, W.C.2    Iyer, R.3    Rana, S.4    Lane, P.5    Ware, R.E.6    Li, D.7    Rees, R.C.8    Investigators, B.-H.9
  • 36
    • 0014360531 scopus 로고
    • Plasma concentrations of hemopexin, haptoglobin and heme in patients with various hemolytic diseases
    • Muller-Eberhard, U., Javid, J., Liem, H.H., Hanstein, A. & Hanna, M. (1968) Plasma concentrations of hemopexin, haptoglobin and heme in patients with various hemolytic diseases. Blood, 32, 811–815.
    • (1968) Blood , vol.32 , pp. 811-815
    • Muller-Eberhard, U.1    Javid, J.2    Liem, H.H.3    Hanstein, A.4    Hanna, M.5
  • 38
    • 84989229018 scopus 로고    scopus 로고
    • Evaluation of biochemical and clinical markers of endothelial dysfunction and their correlation with urinary albumin excretion in patients with type 1 diabetes mellitus
    • Polat, S.B., Ugurlu, N., Aslan, N., Cuhaci, N., Ersoy, R. & Cakir, B. (2016) Evaluation of biochemical and clinical markers of endothelial dysfunction and their correlation with urinary albumin excretion in patients with type 1 diabetes mellitus. Archives of Endocrinology and Metabolism, 60, 117–124.
    • (2016) Archives of Endocrinology and Metabolism , vol.60 , pp. 117-124
    • Polat, S.B.1    Ugurlu, N.2    Aslan, N.3    Cuhaci, N.4    Ersoy, R.5    Cakir, B.6
  • 39
    • 84942504675 scopus 로고    scopus 로고
    • Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease
    • Quimby, K.R., Hambleton, I.R. & Landis, R.C. (2015) Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease. Medical Hypotheses, 85, 424–32.
    • (2015) Medical Hypotheses , vol.85 , pp. 424-432
    • Quimby, K.R.1    Hambleton, I.R.2    Landis, R.C.3
  • 40
    • 85015561270 scopus 로고    scopus 로고
    • The pathophysiology of extracellular hemoglobin associated with enhanced oxidative reactions
    • Rifkind, J.M., Mohanty, J.G. & Nagababu, E. (2014) The pathophysiology of extracellular hemoglobin associated with enhanced oxidative reactions. Frontiers in Physiology, 5, 500.
    • (2014) Frontiers in Physiology , vol.5 , pp. 500
    • Rifkind, J.M.1    Mohanty, J.G.2    Nagababu, E.3
  • 43
    • 84957793098 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease
    • Sasongko, T.H., Nagalla, S. & Ballas, S.K. (2015) Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease. Cochrane Database Systematic Review, 6, CD009191.
    • (2015) Cochrane Database Systematic Review , vol.6 , pp. CD009191
    • Sasongko, T.H.1    Nagalla, S.2    Ballas, S.K.3
  • 44
    • 30144435054 scopus 로고    scopus 로고
    • CD163 is the macrophage scavenger receptor for native and chemically modified hemoglobins in the absence of haptoglobin
    • Schaer, D.J., Schaer, C.A., Buehler, P.W., Boykins, R.A., Schoedon, G., Alayash, A.I. & Schaffner, A. (2006) CD163 is the macrophage scavenger receptor for native and chemically modified hemoglobins in the absence of haptoglobin. Blood, 107, 373–380.
    • (2006) Blood , vol.107 , pp. 373-380
    • Schaer, D.J.1    Schaer, C.A.2    Buehler, P.W.3    Boykins, R.A.4    Schoedon, G.5    Alayash, A.I.6    Schaffner, A.7
  • 45
    • 84874439878 scopus 로고    scopus 로고
    • Hemolysis and free hemoglobin revisited: exploring hemoglobin and hemin scavengers as a novel class of therapeutic proteins
    • Schaer, D.J., Buehler, P.W., Alayash, A.I., Belcher, J.D. & Vercellotti, G.M. (2013) Hemolysis and free hemoglobin revisited: exploring hemoglobin and hemin scavengers as a novel class of therapeutic proteins. Blood, 121, 1276–1284.
    • (2013) Blood , vol.121 , pp. 1276-1284
    • Schaer, D.J.1    Buehler, P.W.2    Alayash, A.I.3    Belcher, J.D.4    Vercellotti, G.M.5
  • 46
    • 84908373728 scopus 로고    scopus 로고
    • Haptoglobin, hemopexin, and related defense pathways-basic science, clinical perspectives, and drug development
    • Schaer, D.J., Vinchi, F., Ingoglia, G., Tolosano, E. & Buehler, P.W. (2014) Haptoglobin, hemopexin, and related defense pathways-basic science, clinical perspectives, and drug development. Frontiers in Physiology, 5, 415.
    • (2014) Frontiers in Physiology , vol.5 , pp. 415
    • Schaer, D.J.1    Vinchi, F.2    Ingoglia, G.3    Tolosano, E.4    Buehler, P.W.5
  • 49
    • 84940029623 scopus 로고    scopus 로고
    • Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders
    • Smith, A. & McCulloh, R.J. (2015) Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders. Frontiers in Physiology, 6, 187.
    • (2015) Frontiers in Physiology , vol.6 , pp. 187
    • Smith, A.1    McCulloh, R.J.2
  • 50
    • 0018634705 scopus 로고
    • Haem transport to the liver by haemopexin. Receptor-mediated uptake with recycling of the protein
    • Smith, A. & Morgan, W.T. (1979) Haem transport to the liver by haemopexin. Receptor-mediated uptake with recycling of the protein. The Biochemical Journal, 182, 47–54.
    • (1979) The Biochemical Journal , vol.182 , pp. 47-54
    • Smith, A.1    Morgan, W.T.2
  • 53
    • 77957359685 scopus 로고    scopus 로고
    • Free heme and the polymerization of sickle cell hemoglobin
    • Uzunova, V.V., Pan, W., Galkin, O. & Vekilov, P.G. (2010) Free heme and the polymerization of sickle cell hemoglobin. Biophysical Journal, 99, 1976–1985.
    • (2010) Biophysical Journal , vol.99 , pp. 1976-1985
    • Uzunova, V.V.1    Pan, W.2    Galkin, O.3    Vekilov, P.G.4
  • 55
    • 84875475916 scopus 로고    scopus 로고
    • Hemopexin therapy improves cardiovascular function by preventing heme-induced endothelial toxicity in mouse models of hemolytic diseases
    • Vinchi, F., De Franceschi, L., Ghigo, A., Townes, T., Cimino, J., Silengo, L., Hirsch, E., Altruda, F. & Tolosano, E. (2013) Hemopexin therapy improves cardiovascular function by preventing heme-induced endothelial toxicity in mouse models of hemolytic diseases. Circulation, 127, 1317–29.
    • (2013) Circulation , vol.127 , pp. 1317-1329
    • Vinchi, F.1    De Franceschi, L.2    Ghigo, A.3    Townes, T.4    Cimino, J.5    Silengo, L.6    Hirsch, E.7    Altruda, F.8    Tolosano, E.9
  • 57
    • 33747152507 scopus 로고    scopus 로고
    • Correction of sickle cell disease by homologous recombination in embryonic stem cells
    • Wu, L.C., Sun, C.W., Ryan, T.M., Pawlik, K.M., Ren, J. & Townes, T.M. (2006) Correction of sickle cell disease by homologous recombination in embryonic stem cells. Blood, 108, 1183–1188.
    • (2006) Blood , vol.108 , pp. 1183-1188
    • Wu, L.C.1    Sun, C.W.2    Ryan, T.M.3    Pawlik, K.M.4    Ren, J.5    Townes, T.M.6
  • 59
    • 84861791408 scopus 로고    scopus 로고
    • Role of extracellular hemoglobin in thrombosis and vascular occlusion in patients with sickle cell anemia
    • Zhou, Z., Behymer, M. & Guchhait, P. (2011) Role of extracellular hemoglobin in thrombosis and vascular occlusion in patients with sickle cell anemia. Anemia, 2011, 918916.
    • (2011) Anemia , vol.2011 , pp. 918916
    • Zhou, Z.1    Behymer, M.2    Guchhait, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.