Regenerative potential of embryonic renal multipotent progenitors in acute renal failure

被引:166
作者
Lazzeri, Elena [1 ]
Crescioli, Clara [1 ]
Ronconi, Elisa [1 ]
Mazzinghi, Benedetta [1 ]
Sagrinati, Costanza [1 ]
Netti, Giuseppe Stefano [3 ]
Angelotti, Maria Lucia [1 ]
Parente, Eliana [1 ]
Ballerini, Lara [1 ]
Cosmi, Lorenzo [1 ]
Maggi, Laura [1 ]
Gesualdo, Loreto [3 ]
Rotondi, Mario [1 ,4 ]
Annunziato, Francesco [1 ]
Maggi, Enrico [1 ]
Lasagni, Laura [1 ]
Serio, Mario [1 ]
Romagnani, Sergio [1 ]
Vannelli, Gabriella Barbara [2 ]
Romagnani, Paola [1 ]
机构
[1] Univ Florence, Excellence Ctr Res, Transfer & High Educ Dev DE NOVO THEREPIES, Florence, Italy
[2] Univ Florence, Dept Anat, Florence, Italy
[3] Univ Foggia, Dept Biomed Sci, Foggia, Italy
[4] Fdn S Maugeri Ist Ricovero & Cura Carattere Sci, Dept Endocrinol & Internal Med, Pavia, Italy
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2007年 / 18卷 / 12期
关键词
D O I
10.1681/ASN.2007020210
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 [临床医学]; 100201 [内科学];
摘要
Bone marrow- and adult kidney-derived stem/progenitor cells hold promise in the development of therapies for renal failure. Here is reported the identification and characterization of renal multipotent progenitors in human embryonic kidneys that share CD24 and CD 133 surface expression with adult renal progenitors and have the capacity for self-renewal and multilineage differentiation. It was found that these CD24(+)CD133(+) cells constitute the early primordial nephron but progressively disappear during nephron development until they become selectively localized to the urinary pole of Bowman's capsule. When isolated and injected into SCID mice with acute renal failure from glycerol-induced rhabdomyolysis, these cells regenerated different portions of the nephron, reduced tissue necrosis and fibrosis, and significantly improved renal function. No tumorigenic potential was observed. It is concluded that CD24(+)CD133(+) cells represent a subset of multipotent embryonic progenitors that persist in human kidneys from early stages of nephrogenesis. The ability of these cells to repair renal damage, together with their apparent lack of tumorigenicity, suggests their potential in the treatment of renal failure.
引用
收藏
页码:3128 / 3138
页数:11
相关论文
共 44 条
[1]
Stem cells in the kidney [J].
Al-Awqati, Q ;
Oliver, JA .
KIDNEY INTERNATIONAL, 2002, 61 (02) :387-395
[2]
Regulatory networks in embryo-derived pluripotent stem cells [J].
Boiani, M ;
Schöler, HR .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (11) :872-884
[3]
Isolation of renal progenitor cells from adult human kidney [J].
Bussolati, B ;
Bruno, S ;
Grange, C ;
Buttiglieri, S ;
Deregibus, MC ;
Cantino, D ;
Camussi, G .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (02) :545-555
[4]
Adult stem cells in the repair of the injured renal tubule [J].
Cantley, LG .
NATURE CLINICAL PRACTICE NEPHROLOGY, 2005, 1 (01) :22-32
[5]
Identifying the molecular phenotype of renal progenitor cells [J].
Challen, GA ;
Martinez, G ;
Davis, MJ ;
Taylor, DF ;
Crowe, M ;
Teasdale, RD ;
Grimmond, SM ;
Little, MH .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (09) :2344-2357
[6]
Kidney side population reveals multilineage potential and renal functional capacity but also cellular heterogeneity [J].
Challen, Grant A. ;
Bertoncello, Ivan ;
Deane, James A. ;
Ricardo, Sharon D. ;
Little, Melissa H. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (07) :1896-1912
[7]
Embryonic committed stem cells as a solution to kidney donor shortage [J].
Dekel, B ;
Reisner, Y .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (04) :443-454
[8]
Human and porcine early kidney precursors as a new source for transplantation [J].
Dekel, B ;
Burakova, T ;
Arditti, FD ;
Reich-Zeliger, S ;
Milstein, O ;
Aviel-Ronen, S ;
Rechavi, G ;
Friedman, N ;
Kaminski, N ;
Passwell, JH ;
Reisner, Y .
NATURE MEDICINE, 2003, 9 (01) :53-60
[9]
Isolation and characterization of nontubular Sca-1+Lin- multipotent stem/progenitor cells from adult mouse kidney [J].
Dekel, Benjamin ;
Zangi, Lior ;
Shezen, Elias ;
Reich-Zeliger, Shlomit ;
Eventov-Friedman, Smadar ;
Katchman, Helena ;
Jacob-Hirsch, Jasmin ;
Amariglio, Ninette ;
Rechavi, Gideon ;
Margalit, Raanan ;
Reisner, Yair .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (12) :3300-3314
[10]
Transplantation of human hematopoietic stem cells into ischemic and growing kidneys suggests a role in vasculogenesis but not tubulogenesis [J].
Dekel, Benjamin ;
Shezen, Elias ;
Even-Tov-Friedman, Smadar ;
Katchman, Helena ;
Margalit, Raanan ;
Nagler, Arnon ;
Reisner, Yair .
STEM CELLS, 2006, 24 (05) :1185-1193