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Erschienen in: Journal of Nephrology 2/2023

09.01.2023 | Original Article

Glomerular expression and urinary excretion of fatty acid-binding protein 4 in IgA nephropathy

verfasst von: Marenao Tanaka, Norihito Moniwa, Chieko Nogi, Toshiki Kano, Megumi Matsumoto, Akiko Sakai, Takuto Maeda, Hideki Takizawa, Yayoi Ogawa, Katsuhiko Asanuma, Yusuke Suzuki, Masato Furuhashi

Erschienen in: Journal of Nephrology | Ausgabe 2/2023

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Abstract

Background

Fatty acid-binding protein 4 (FABP4) is secreted from adipocytes and macrophages in adipose tissue and acts as an adipokine. It has recently been reported that FABP4, but not liver-type FABP (L-FABP/FABP1), is also expressed in injured glomerular endothelial cells and infiltrating macrophages in the glomerulus and that urinary FABP4 (U-FABP4) is associated with proteinuria and kidney function impairment in nephrotic patients. However, the link between glomerular FABP4 and U-FABP4 has not been fully addressed in IgA nephropathy (IgAN).

Methods

We investigated the involvement of FABP4 in human and mouse IgAN.

Results

In patients with IgAN (n = 23), the ratio of FABP4-positive area to total area within glomeruli (G-FABP4-Area) and U-FABP4 were positively correlated with proteinuria and were negatively correlated with eGFR. In 4–28-week-old male grouped ddY mice, a spontaneous IgAN-prone mouse model, FABP4 was detected in glomerular endothelial cells and macrophages, and G-FABP4-Area was positively correlated with urinary albumin-to-creatinine ratio (r = 0.957, P < 0.001). Endoplasmic reticulum stress markers were detected in glomeruli of human and mouse IgAN. In human renal glomerular endothelial cells, FABP4 was induced by treatment with vascular endothelial growth factor and was secreted from the cells. Treatment of human renal glomerular endothelial cells or mouse podocytes with palmitate-bound recombinant FABP4 significantly increased gene expression of inflammatory cytokines and endoplasmic reticulum stress markers, and the effects of FABP4 in podocytes were attenuated in the presence of an anti-FABP4 antibody.

Conclusion

FABP4 in the glomerulus contributes to proteinuria in IgAN, and U-FABP4 level is a useful surrogate biomarker for glomerular damage in IgAN.
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Literatur
2.
Zurück zum Zitat Pattrapornpisut P, Avila-Casado C, Reich HN (2021) IgA nephropathy: core curriculum 2021. Am J Kidney Dis 78:429–441PubMed Pattrapornpisut P, Avila-Casado C, Reich HN (2021) IgA nephropathy: core curriculum 2021. Am J Kidney Dis 78:429–441PubMed
3.
Zurück zum Zitat Koyama A, Igarashi M, Kobayashi M (1997) Natural history and risk factors for immunoglobulin A nephropathy in Japan. Research Group on Progressive Renal Diseases. Am J Kidney Dis 29:526–532PubMed Koyama A, Igarashi M, Kobayashi M (1997) Natural history and risk factors for immunoglobulin A nephropathy in Japan. Research Group on Progressive Renal Diseases. Am J Kidney Dis 29:526–532PubMed
4.
Zurück zum Zitat Ruan XZ, Varghese Z, Moorhead JF (2009) An update on the lipid nephrotoxicity hypothesis. Nat Rev Nephrol 5:713–721PubMed Ruan XZ, Varghese Z, Moorhead JF (2009) An update on the lipid nephrotoxicity hypothesis. Nat Rev Nephrol 5:713–721PubMed
5.
Zurück zum Zitat Izquierdo-Lahuerta A, Martinez-Garcia C, Medina-Gomez G (2016) Lipotoxicity as a trigger factor of renal disease. J Nephrol 29:603–610PubMed Izquierdo-Lahuerta A, Martinez-Garcia C, Medina-Gomez G (2016) Lipotoxicity as a trigger factor of renal disease. J Nephrol 29:603–610PubMed
6.
Zurück zum Zitat Osanami A, Tanaka M, Furuhashi M et al (2022) Increased LDL cholesterol level is associated with deterioration of renal function in males. Clin Kidney J 15:1888–1895PubMedCentralPubMed Osanami A, Tanaka M, Furuhashi M et al (2022) Increased LDL cholesterol level is associated with deterioration of renal function in males. Clin Kidney J 15:1888–1895PubMedCentralPubMed
7.
Zurück zum Zitat Gregor MF, Hotamisligil GS (2011) Inflammatory mechanisms in obesity. Annu Rev Immunol 29:415–445PubMed Gregor MF, Hotamisligil GS (2011) Inflammatory mechanisms in obesity. Annu Rev Immunol 29:415–445PubMed
8.
Zurück zum Zitat Hotamisligil GS (2017) Inflammation, metaflammation and immunometabolic disorders. Nature 542:177–185PubMed Hotamisligil GS (2017) Inflammation, metaflammation and immunometabolic disorders. Nature 542:177–185PubMed
9.
Zurück zum Zitat Urano F, Wang X, Bertolotti A et al (2000) Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1. Science 287:664–666PubMed Urano F, Wang X, Bertolotti A et al (2000) Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1. Science 287:664–666PubMed
10.
Zurück zum Zitat Deng J, Lu PD, Zhang Y et al (2004) Translational repression mediates activation of nuclear factor kappa B by phosphorylated translation initiation factor 2. Mol Cell Biol 24:10161–10168PubMedCentralPubMed Deng J, Lu PD, Zhang Y et al (2004) Translational repression mediates activation of nuclear factor kappa B by phosphorylated translation initiation factor 2. Mol Cell Biol 24:10161–10168PubMedCentralPubMed
11.
Zurück zum Zitat Hu P, Han Z, Couvillon AD et al (2006) Autocrine tumor necrosis factor alpha links endoplasmic reticulum stress to the membrane death receptor pathway through IRE1alpha-mediated NF-kappaB activation and down-regulation of TRAF2 expression. Mol Cell Biol 26:3071–3084PubMedCentralPubMed Hu P, Han Z, Couvillon AD et al (2006) Autocrine tumor necrosis factor alpha links endoplasmic reticulum stress to the membrane death receptor pathway through IRE1alpha-mediated NF-kappaB activation and down-regulation of TRAF2 expression. Mol Cell Biol 26:3071–3084PubMedCentralPubMed
12.
Zurück zum Zitat Ozcan U, Yilmaz E, Ozcan L et al (2006) Chemical chaperones reduce ER stress and restore glucose homeostasis in a mouse model of type 2 diabetes. Science 313:1137–1140PubMedCentralPubMed Ozcan U, Yilmaz E, Ozcan L et al (2006) Chemical chaperones reduce ER stress and restore glucose homeostasis in a mouse model of type 2 diabetes. Science 313:1137–1140PubMedCentralPubMed
13.
Zurück zum Zitat Ishimura S, Furuhashi M, Mita T et al (2014) Reduction of endoplasmic reticulum stress inhibits neointima formation after vascular injury. Sci Rep 4:6943PubMedCentralPubMed Ishimura S, Furuhashi M, Mita T et al (2014) Reduction of endoplasmic reticulum stress inhibits neointima formation after vascular injury. Sci Rep 4:6943PubMedCentralPubMed
14.
Zurück zum Zitat Koyama M, Furuhashi M, Ishimura S et al (2014) Reduction of endoplasmic reticulum stress by 4-phenylbutyric acid prevents the development of hypoxia-induced pulmonary arterial hypertension. Am J Physiol Heart Circ Physiol 306:H1314-1323PubMed Koyama M, Furuhashi M, Ishimura S et al (2014) Reduction of endoplasmic reticulum stress by 4-phenylbutyric acid prevents the development of hypoxia-induced pulmonary arterial hypertension. Am J Physiol Heart Circ Physiol 306:H1314-1323PubMed
15.
Zurück zum Zitat Furuhashi M, Hotamisligil GS (2008) Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discov 7:489–503PubMedCentralPubMed Furuhashi M, Hotamisligil GS (2008) Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discov 7:489–503PubMedCentralPubMed
16.
Zurück zum Zitat Furuhashi M (2019) Fatty acid-binding protein 4 in cardiovascular and metabolic diseases. J Atheroscler Thromb 26:216–232PubMedCentralPubMed Furuhashi M (2019) Fatty acid-binding protein 4 in cardiovascular and metabolic diseases. J Atheroscler Thromb 26:216–232PubMedCentralPubMed
17.
Zurück zum Zitat Kamijo A, Kimura K, Sugaya T et al (2002) Urinary free fatty acids bound to albumin aggravate tubulointerstitial damage. Kidney Int 62:1628–1637PubMed Kamijo A, Kimura K, Sugaya T et al (2002) Urinary free fatty acids bound to albumin aggravate tubulointerstitial damage. Kidney Int 62:1628–1637PubMed
18.
Zurück zum Zitat Kamijo A, Kimura K, Sugaya T et al (2004) Urinary fatty acid-binding protein as a new clinical marker of the progression of chronic renal disease. J Lab Clin Med 143:23–30PubMed Kamijo A, Kimura K, Sugaya T et al (2004) Urinary fatty acid-binding protein as a new clinical marker of the progression of chronic renal disease. J Lab Clin Med 143:23–30PubMed
19.
Zurück zum Zitat Kamijo-Ikemori A, Sugaya T, Kimura K (2014) Novel urinary biomarkers in early diabetic kidney disease. Curr Diab Rep 14:513PubMed Kamijo-Ikemori A, Sugaya T, Kimura K (2014) Novel urinary biomarkers in early diabetic kidney disease. Curr Diab Rep 14:513PubMed
20.
Zurück zum Zitat Furuhashi M, Tuncman G, Gorgun CZ et al (2007) Treatment of diabetes and atherosclerosis by inhibiting fatty-acid-binding protein aP2. Nature 447:959–965PubMedCentralPubMed Furuhashi M, Tuncman G, Gorgun CZ et al (2007) Treatment of diabetes and atherosclerosis by inhibiting fatty-acid-binding protein aP2. Nature 447:959–965PubMedCentralPubMed
21.
Zurück zum Zitat Ishimura S, Furuhashi M, Watanabe Y et al (2013) Circulating levels of fatty acid-binding protein family and metabolic phenotype in the general population. PLoS ONE 8:e81318PubMedCentralPubMed Ishimura S, Furuhashi M, Watanabe Y et al (2013) Circulating levels of fatty acid-binding protein family and metabolic phenotype in the general population. PLoS ONE 8:e81318PubMedCentralPubMed
22.
Zurück zum Zitat Fuseya T, Furuhashi M, Matsumoto M et al (2017) Ectopic fatty acid-binding protein 4 expression in the vascular endothelium is involved in neointima formation after vascular injury. J Am Heart Assoc 6:e006377PubMedCentralPubMed Fuseya T, Furuhashi M, Matsumoto M et al (2017) Ectopic fatty acid-binding protein 4 expression in the vascular endothelium is involved in neointima formation after vascular injury. J Am Heart Assoc 6:e006377PubMedCentralPubMed
23.
Zurück zum Zitat Tanaka M, Furuhashi M, Okazaki Y et al (2014) Ectopic expression of fatty acid-binding protein 4 in the glomerulus is associated with proteinuria and renal dysfunction. Nephron Clin Pract 128:345–351PubMed Tanaka M, Furuhashi M, Okazaki Y et al (2014) Ectopic expression of fatty acid-binding protein 4 in the glomerulus is associated with proteinuria and renal dysfunction. Nephron Clin Pract 128:345–351PubMed
24.
Zurück zum Zitat Okazaki Y, Furuhashi M, Tanaka M et al (2014) Urinary excretion of fatty acid-binding protein 4 is associated with albuminuria and renal dysfunction. PLoS ONE 9:e115429PubMedCentralPubMed Okazaki Y, Furuhashi M, Tanaka M et al (2014) Urinary excretion of fatty acid-binding protein 4 is associated with albuminuria and renal dysfunction. PLoS ONE 9:e115429PubMedCentralPubMed
25.
Zurück zum Zitat Tanaka M, Furuhashi M, Moniwa N et al (2020) Significance of urinary fatty acid-binding protein 4 level as a possible biomarker for the identification of minimal change disease in patents with nephrotic-range proteinuria. BMC Nephrol 21:459PubMedCentralPubMed Tanaka M, Furuhashi M, Moniwa N et al (2020) Significance of urinary fatty acid-binding protein 4 level as a possible biomarker for the identification of minimal change disease in patents with nephrotic-range proteinuria. BMC Nephrol 21:459PubMedCentralPubMed
26.
Zurück zum Zitat KDIGO (2012) Chapter 10: Immunoglobulin A nephropathy. Kidney Int Suppl 2:209–217 KDIGO (2012) Chapter 10: Immunoglobulin A nephropathy. Kidney Int Suppl 2:209–217
27.
Zurück zum Zitat Yuzawa Y, Yamamoto R, Takahashi K et al (2016) Evidence-based clinical practice guidelines for IgA nephropathy 2014. Clin Exp Nephrol 20:511–535PubMedCentralPubMed Yuzawa Y, Yamamoto R, Takahashi K et al (2016) Evidence-based clinical practice guidelines for IgA nephropathy 2014. Clin Exp Nephrol 20:511–535PubMedCentralPubMed
28.
Zurück zum Zitat Matsuo S, Imai E, Horio M et al (2009) Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis 53:982–992PubMed Matsuo S, Imai E, Horio M et al (2009) Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis 53:982–992PubMed
29.
Zurück zum Zitat Xu A, Wang Y, Xu JY et al (2006) Adipocyte fatty acid-binding protein is a plasma biomarker closely associated with obesity and metabolic syndrome. Clin Chem 52:405–413PubMed Xu A, Wang Y, Xu JY et al (2006) Adipocyte fatty acid-binding protein is a plasma biomarker closely associated with obesity and metabolic syndrome. Clin Chem 52:405–413PubMed
30.
Zurück zum Zitat Suzuki H, Suzuki Y (2018) Murine models of human IgA nephropathy. Semin Nephrol 38:513–520PubMed Suzuki H, Suzuki Y (2018) Murine models of human IgA nephropathy. Semin Nephrol 38:513–520PubMed
31.
Zurück zum Zitat Okazaki K, Suzuki Y, Otsuji M et al (2012) Development of a model of early-onset IgA nephropathy. J Am Soc Nephrol 23:1364–1374PubMedCentralPubMed Okazaki K, Suzuki Y, Otsuji M et al (2012) Development of a model of early-onset IgA nephropathy. J Am Soc Nephrol 23:1364–1374PubMedCentralPubMed
32.
Zurück zum Zitat Mundel P, Reiser J, Zuniga Mejia Borja A et al (1997) Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines. Exp Cell Res 236:248–258PubMed Mundel P, Reiser J, Zuniga Mejia Borja A et al (1997) Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines. Exp Cell Res 236:248–258PubMed
33.
Zurück zum Zitat Asanuma K, Shirato I, Ishidoh K et al (2002) Selective modulation of the secretion of proteinases and their inhibitors by growth factors in cultured differentiated podocytes. Kidney Int 62:822–831PubMed Asanuma K, Shirato I, Ishidoh K et al (2002) Selective modulation of the secretion of proteinases and their inhibitors by growth factors in cultured differentiated podocytes. Kidney Int 62:822–831PubMed
34.
Zurück zum Zitat Furuhashi M, Mita T, Moniwa N et al (2015) Angiotensin II receptor blockers decrease serum concentration of fatty acid-binding protein 4 in patients with hypertension. Hypertens Res 38:252–259PubMed Furuhashi M, Mita T, Moniwa N et al (2015) Angiotensin II receptor blockers decrease serum concentration of fatty acid-binding protein 4 in patients with hypertension. Hypertens Res 38:252–259PubMed
35.
Zurück zum Zitat Mita T, Furuhashi M, Hiramitsu S et al (2015) FABP4 is secreted from adipocytes by adenyl cyclase-PKA- and guanylyl cyclase-PKG-dependent lipolytic mechanisms. Obesity (Silver Spring) 23:359–367PubMed Mita T, Furuhashi M, Hiramitsu S et al (2015) FABP4 is secreted from adipocytes by adenyl cyclase-PKA- and guanylyl cyclase-PKG-dependent lipolytic mechanisms. Obesity (Silver Spring) 23:359–367PubMed
36.
Zurück zum Zitat Kanda Y (2013) Investigation of the freely available easy-to-use software “EZR” for medical statistics. Bone Marrow Transplant 48:452–458PubMed Kanda Y (2013) Investigation of the freely available easy-to-use software “EZR” for medical statistics. Bone Marrow Transplant 48:452–458PubMed
37.
Zurück zum Zitat Elmasri H, Karaaslan C, Teper Y et al (2009) Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J 23:3865–3873PubMedCentralPubMed Elmasri H, Karaaslan C, Teper Y et al (2009) Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J 23:3865–3873PubMedCentralPubMed
38.
Zurück zum Zitat Elmasri H, Ghelfi E, Yu CW et al (2012) Endothelial cell-fatty acid binding protein 4 promotes angiogenesis: role of stem cell factor/c-kit pathway. Angiogenesis 15:457–468PubMedCentralPubMed Elmasri H, Ghelfi E, Yu CW et al (2012) Endothelial cell-fatty acid binding protein 4 promotes angiogenesis: role of stem cell factor/c-kit pathway. Angiogenesis 15:457–468PubMedCentralPubMed
39.
Zurück zum Zitat Furuhashi M, Fuseya T, Murata M et al (2016) Local production of fatty acid-binding protein 4 in epicardial/perivascular fat and macrophages is linked to coronary atherosclerosis. Arterioscler Thromb Vasc Biol 36:825–834PubMed Furuhashi M, Fuseya T, Murata M et al (2016) Local production of fatty acid-binding protein 4 in epicardial/perivascular fat and macrophages is linked to coronary atherosclerosis. Arterioscler Thromb Vasc Biol 36:825–834PubMed
40.
Zurück zum Zitat Yao F, Li Z, Ehara T et al (2015) Fatty Acid-Binding Protein 4 mediates apoptosis via endoplasmic reticulum stress in mesangial cells of diabetic nephropathy. Mol Cell Endocrinol 411:232–242PubMed Yao F, Li Z, Ehara T et al (2015) Fatty Acid-Binding Protein 4 mediates apoptosis via endoplasmic reticulum stress in mesangial cells of diabetic nephropathy. Mol Cell Endocrinol 411:232–242PubMed
41.
Zurück zum Zitat Prentice KJ, Saksi J, Robertson LT et al (2021) A hormone complex of FABP4 and nucleoside kinases regulates islet function. Nature 600:720–726PubMedCentralPubMed Prentice KJ, Saksi J, Robertson LT et al (2021) A hormone complex of FABP4 and nucleoside kinases regulates islet function. Nature 600:720–726PubMedCentralPubMed
42.
Zurück zum Zitat D’Amico G (2004) Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome. Semin Nephrol 24:179–196PubMed D’Amico G (2004) Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome. Semin Nephrol 24:179–196PubMed
43.
Zurück zum Zitat Hotta O, Miyazaki M, Furuta T et al (2001) Tonsillectomy and steroid pulse therapy significantly impact on clinical remission in patients with IgA nephropathy. Am J Kidney Dis 38:736–743PubMed Hotta O, Miyazaki M, Furuta T et al (2001) Tonsillectomy and steroid pulse therapy significantly impact on clinical remission in patients with IgA nephropathy. Am J Kidney Dis 38:736–743PubMed
44.
Zurück zum Zitat Pozzi C, Andrulli S, Del Vecchio L et al (2004) Corticosteroid effectiveness in IgA nephropathy: long-term results of a randomized, controlled trial. J Am Soc Nephrol 15:157–163PubMed Pozzi C, Andrulli S, Del Vecchio L et al (2004) Corticosteroid effectiveness in IgA nephropathy: long-term results of a randomized, controlled trial. J Am Soc Nephrol 15:157–163PubMed
45.
Zurück zum Zitat Kawamura T, Yoshimura M, Miyazaki Y et al (2014) A multicenter randomized controlled trial of tonsillectomy combined with steroid pulse therapy in patients with immunoglobulin A nephropathy. Nephrol Dial Transplant 29:1546–1553PubMedCentralPubMed Kawamura T, Yoshimura M, Miyazaki Y et al (2014) A multicenter randomized controlled trial of tonsillectomy combined with steroid pulse therapy in patients with immunoglobulin A nephropathy. Nephrol Dial Transplant 29:1546–1553PubMedCentralPubMed
46.
Zurück zum Zitat Hirano K, Matsuzaki K, Yasuda T et al (2019) Association between tonsillectomy and outcomes in patients with immunoglobulin A nephropathy. JAMA Netw Open 2:e194772PubMedCentralPubMed Hirano K, Matsuzaki K, Yasuda T et al (2019) Association between tonsillectomy and outcomes in patients with immunoglobulin A nephropathy. JAMA Netw Open 2:e194772PubMedCentralPubMed
47.
Zurück zum Zitat Medjeral-Thomas NR, O’Shaughnessy MM (2020) Complement in IgA nephropathy: the role of complement in the pathogenesis, diagnosis, and future management of IgA nephropathy. Adv Chronic Kidney Dis 27:111–119PubMed Medjeral-Thomas NR, O’Shaughnessy MM (2020) Complement in IgA nephropathy: the role of complement in the pathogenesis, diagnosis, and future management of IgA nephropathy. Adv Chronic Kidney Dis 27:111–119PubMed
48.
Zurück zum Zitat Zhao N, Hou P, Lv J et al (2012) The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression. Kidney Int 82:790–796PubMedCentralPubMed Zhao N, Hou P, Lv J et al (2012) The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression. Kidney Int 82:790–796PubMedCentralPubMed
49.
Zurück zum Zitat Suzuki H, Allegri L, Suzuki Y et al (2016) Galactose-deficient IgA1 as a candidate urinary polypeptide marker of IgA nephropathy? Dis Markers 2016:7806438PubMedCentralPubMed Suzuki H, Allegri L, Suzuki Y et al (2016) Galactose-deficient IgA1 as a candidate urinary polypeptide marker of IgA nephropathy? Dis Markers 2016:7806438PubMedCentralPubMed
50.
Zurück zum Zitat Irabu H, Shimizu M, Kaneko S et al (2021) Apoptosis inhibitor of macrophage as a biomarker for disease activity in Japanese children with IgA nephropathy and Henoch-Schonlein purpura nephritis. Pediatr Res 89:667–672PubMed Irabu H, Shimizu M, Kaneko S et al (2021) Apoptosis inhibitor of macrophage as a biomarker for disease activity in Japanese children with IgA nephropathy and Henoch-Schonlein purpura nephritis. Pediatr Res 89:667–672PubMed
51.
Zurück zum Zitat Takahata A, Arai S, Hiramoto E et al (2020) Crucial role of AIM/CD5L in the development of glomerular inflammation in IgA nephropathy. J Am Soc Nephrol 31:2013–2024PubMedCentralPubMed Takahata A, Arai S, Hiramoto E et al (2020) Crucial role of AIM/CD5L in the development of glomerular inflammation in IgA nephropathy. J Am Soc Nephrol 31:2013–2024PubMedCentralPubMed
52.
Zurück zum Zitat Tomino Y (2016) Diagnosis and treatment of patients with IgA nephropathy in Japan. Kidney Res Clin Pract 35:197–203PubMedCentralPubMed Tomino Y (2016) Diagnosis and treatment of patients with IgA nephropathy in Japan. Kidney Res Clin Pract 35:197–203PubMedCentralPubMed
53.
Zurück zum Zitat Obajdin J, Cotter M, Snelling S et al (2018) Fatty-acid binding protein 4 (FABP4) as a potential preclinical biomarker of drug-induced kidney injury. Toxicol Sci 166:441–450PubMed Obajdin J, Cotter M, Snelling S et al (2018) Fatty-acid binding protein 4 (FABP4) as a potential preclinical biomarker of drug-induced kidney injury. Toxicol Sci 166:441–450PubMed
54.
Zurück zum Zitat Shrestha S, Sunaga H, Hanaoka H et al (2018) Circulating FABP4 is eliminated by the kidney via glomerular filtration followed by megalin-mediated reabsorption. Sci Rep 8:16451PubMedCentralPubMed Shrestha S, Sunaga H, Hanaoka H et al (2018) Circulating FABP4 is eliminated by the kidney via glomerular filtration followed by megalin-mediated reabsorption. Sci Rep 8:16451PubMedCentralPubMed
Metadaten
Titel
Glomerular expression and urinary excretion of fatty acid-binding protein 4 in IgA nephropathy
verfasst von
Marenao Tanaka
Norihito Moniwa
Chieko Nogi
Toshiki Kano
Megumi Matsumoto
Akiko Sakai
Takuto Maeda
Hideki Takizawa
Yayoi Ogawa
Katsuhiko Asanuma
Yusuke Suzuki
Masato Furuhashi
Publikationsdatum
09.01.2023
Verlag
Springer International Publishing
Erschienen in
Journal of Nephrology / Ausgabe 2/2023
Print ISSN: 1121-8428
Elektronische ISSN: 1724-6059
DOI
https://doi.org/10.1007/s40620-022-01551-2

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