The L1 cell adhesion molecule is a potential biomarker of human distal nephron injury in acute tubular necrosis

被引:16
作者
Allory, Y. [1 ,2 ,3 ]
Audard, V. [4 ,5 ]
Fontanges, P. [3 ]
Ronco, P. [1 ,2 ,3 ]
Debiec, H. [1 ,2 ]
机构
[1] Hop Tenon, INSERM, U702, AP HP,Dept Nephrol, F-75020 Paris, France
[2] INSERM, UMR S 702, Paris, France
[3] Univ Paris 06, Paris, France
[4] Dept Nephrol, Paris, France
[5] Univ Paris 12, Inst Rech & Nephrol & Transplantat France, Hop Henri Mondor, Paris, France
关键词
L1 cell adhesion molecule; acute kidney injury; acute tubular necrosis; urine; biological markers;
D O I
10.1038/sj.ki.5002640
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The L1 cell adhesion molecule (CD171) is a multidomain membrane glycoprotein of the immunoglobulin superfamily. We evaluated its expression in human acute kidney injury and assessed its use as a tissue and urinary marker of acute tubular injury. Using immunohistochemical studies with antibodies to the extracellular or cytoplasmic domains, we compared L1 expression in normal kidneys in 24 biopsies taken from patients with acute tubular necrosis. L1 was found at the basolateral and the lateral membrane in all epithelial cells of the collecting duct in the normal kidney except for intercalated cells. In acute tubular necrosis, L1 lost its polarized distribution being found in both the basolateral and apical domains of the collecting duct. Further, it was induced in thick ascending limb and distal tubule cells. Apically expressed L1 found only when the cytoplasmic domain antibody was used in biopsy specimens of patients with acute tubular necrosis. The levels of urinary L1, normalized for creatinine, were significantly higher in all 24 patients with acute tubular necrosis compared to five patients with prerenal azotemia or to six patients with other causes of acute kidney injury. Our study shows that a soluble form of human L1 can be detected in the urine of patients with acute tubular necrosis and that this may be a marker of distal nephron injury.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 46 条
  • [1] Expression of NCAM recapitulates tubulogenic development in kidneys recovering from acute ischemia
    Abbate, M
    Brown, D
    Bonventre, JV
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (03) : F454 - F463
  • [2] NITRIC-OXIDE AND PROSTANOIDS PROTECT THE RENAL OUTER MEDULLA FROM RADIOCONTRAST TOXICITY IN THE RAT
    AGMON, Y
    PELEG, H
    GREENFELD, Z
    ROSEN, S
    BREZIS, M
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (03) : 1069 - 1075
  • [3] Allory Y, 2005, CLIN CANCER RES, V11, P1190
  • [4] Shedding of kidney injury molecule-1, a putative adhesion protein involved in renal regeneration
    Bailly, V
    Zhang, ZW
    Meier, W
    Cate, R
    Sanicola, M
    Bonventre, JV
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) : 39739 - 39748
  • [5] Neural cell recognition molecule L1:: from cell biology to human hereditary brain malformations
    Brümmendorf, T
    Kenwrick, S
    Rathjen, FG
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 1998, 8 (01) : 87 - 97
  • [6] The cell adhesion molecule L1 is developmentally regulated in the renal epithelium and is involved in kidney branching morphogenesis
    Debiec, H
    Christensen, EI
    Ronco, PM
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 143 (07) : 2067 - 2079
  • [7] Diagnosis and treatment of acute tubular necrosis
    Esson, ML
    Schrier, RW
    [J]. ANNALS OF INTERNAL MEDICINE, 2002, 137 (09) : 744 - 752
  • [8] DISRUPTION OF EPITHELIAL CELL-MATRIX INTERACTIONS INDUCES APOPTOSIS
    FRISCH, SM
    FRANCIS, H
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 124 (04) : 619 - 626
  • [9] REDISTRIBUTION AND DYSFUNCTION OF INTEGRINS IN CULTURED RENAL EPITHELIAL-CELLS EXPOSED TO OXIDATIVE STRESS
    GAILIT, J
    COLFLESH, D
    RABINER, I
    SIMONE, J
    GOLIGORSKY, MS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (01): : F149 - F157
  • [10] Cleavage of L1 in exosomes and apoptotic membrane vesicles released from ovarian carcinoma cells
    Gutwein, P
    Stoeck, A
    Riedle, S
    Gast, D
    Runz, S
    Condon, TP
    Marmé, A
    Phong, MC
    Linderkamp, O
    Skorokhod, A
    Altevogt, P
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (07) : 2492 - 2501