CD10 in the developing human kidney: immunoreactivity and possible role in renal embryogenesis

被引:22
作者
Faa, G. [1 ]
Gerosa, C. [1 ]
Fanni, D. [1 ]
Nemolato, S. [1 ]
Marinelli, V. [2 ]
Locci, A. [1 ]
Senes, G. [1 ]
Mais, V. [3 ]
Van Eyken, P. [4 ]
Iacovidou, N. [5 ]
Monga, G. [6 ]
Fanos, V. [2 ]
机构
[1] Univ Cagliari, Dept Pathol, Cagliari, Italy
[2] Univ Cagliari, Dept Pediat & Clin Med, NICU, Cagliari, Italy
[3] Univ Cagliari, Dept Surg Maternal Fetal Med & Imaging, Cagliari, Italy
[4] Katholieke Univ Leuven, Dept Pathol, Louvain, Belgium
[5] Univ Athens, GR-10679 Athens, Greece
[6] Univ Piemonte Orientale, Dept Pathol, Novara, Italy
关键词
Embryo; fetus; glomerulogenesis; nephrogenesis; preterm; LYMPHOBLASTIC-LEUKEMIA ANTIGEN; CELL CARCINOMA; EXPRESS; TISSUE; FETAL; RCC; KEY;
D O I
10.3109/14767058.2011.599457
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
CD10 was first identified in tumor cells of acute lymphoblastic leukemia. Most studies on CD10 expression have dealt with tumor pathology. Since no data are available for specific role in the fetal kidney, this study aimed at investigating CD10 expression during the different phases of renal embryogenesis. To this end, the expression of CD10 was evaluated in the kidney of two human fetus and in three newborns. In both fetuses, immunostaining for CD10 was compartmentalized and mainly concentrated in the mid-deep cortex. Reactivity for CD10 was stronger in the glomerular epithelium, in proximal tubules and in metanephric mesenchymal cells. At 25 weeks of gestation, CD10 was also detected in the subcapsular regions, including some pretubular aggregates of cap mesenchymal cells and renal vesicles. At 34 weeks of gestation, we observed an increased immunoreactivity for CD10 in visceral and parietal glomerular epithelium. At 39 weeks of gestation, CD10 was also expressed in the collecting tubules and in the Henle loops. Our data show a strong expression of CD10 in all stage of human kidney development, characterized by dynamic changes and support the hypothesis that CD10 plays a relevant role in renal embryogenesis.
引用
收藏
页码:904 / 911
页数:8
相关论文
共 20 条
[1]   Use of antibodies to RCC and CD10 in the differential diagnosis of renal neoplasms [J].
Avery, AK ;
Beckstead, J ;
Renshaw, AA ;
Corless, CL .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (02) :203-210
[2]   The CD10 Enzyme Is a Key Player to Identify and Regulate Human Mammary Stem Cells [J].
Bachelard-Cascales, Elodie ;
Chapellier, Marion ;
Delay, Emmanuel ;
Pochon, Gaetan ;
Voeltzel, Thibault ;
Puisieux, Alain ;
de Fromentel, Claude Caron ;
Maguer-Satta, Veronique .
STEM CELLS, 2010, 28 (06) :1081-1088
[3]  
BRAUN MP, 1983, BLOOD, V61, P718
[4]   Marked interindividual variability in renal maturation of preterm infants: lessons from autopsy [J].
Faa, Gavino ;
Gerosa, Clara ;
Fanni, Daniela ;
Nemolato, Sonia ;
Locci, Annalisa ;
Cabras, Tiziana ;
Marinelli, Viviana ;
Puddu, Melania ;
Zaffanello, Marco ;
Monga, Guido ;
Fanos, Vassilios .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2010, 23 :129-133
[5]   ANTISERA TO ACUTE LYMPHOBLASTIC LEUKEMIA-CELLS [J].
GREAVES, MF ;
BROWN, G ;
RAPSON, NT ;
LISTER, TA .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1975, 4 (01) :67-84
[6]   PURIFICATION AND CHARACTERIZATION OF FETAL HEMATOPOIETIC-CELLS THAT EXPRESS THE COMMON ACUTE LYMPHOBLASTIC-LEUKEMIA ANTIGEN (CALLA) [J].
HOKLAND, P ;
ROSENTHAL, P ;
GRIFFIN, JD ;
NADLER, LM ;
DALEY, J ;
HOKLAND, M ;
SCHLOSSMAN, SF ;
RITZ, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (01) :114-129
[7]   The Density of CD10 Corresponds to Commitment and Progression in the Human B Lymphoid Lineage [J].
Ichii, Michiko ;
Oritani, Kenji ;
Yokota, Takafumi ;
Zhang, Qingzhao ;
Garrett, Karla P. ;
Kanakura, Yuzuru ;
Kincade, Paul W. .
PLOS ONE, 2010, 5 (09)
[8]  
Little M, 2010, 11 INT WORKSH DEV NE
[9]   Concise Review: Neutral Endopeptidase (CD10): A Multifaceted Environment Actor in Stem Cells, Physiological Mechanisms, and Cancer [J].
Maguer-Satta, Veronique ;
Besancon, Roger ;
Bachelard-Cascales, Elodie .
STEM CELLS, 2011, 29 (03) :389-396
[10]   CD10 is expressed in a subset of chromophobe renal cell carcinomas [J].
Martignoni, G ;
Pea, M ;
Brunelli, M ;
Chilosi, M ;
Zamó, A ;
Bertaso, M ;
Cossu-Rocca, P ;
Eble, JN ;
Mikuz, G ;
Puppa, G ;
Badoual, C ;
Ficarra, V ;
Novella, G ;
Bonetti, F .
MODERN PATHOLOGY, 2004, 17 (12) :1455-1463