Podocytes in culture: past, present, and future

被引:300
作者
Shankland, S. J.
Pippin, J. W.
Reiser, J.
Mundel, P.
机构
[1] Univ Washington, Dept Med, Div Nephrol, Seattle, WA 98195 USA
[2] Massachusetts Gen Hosp, Dept Med, Div Nephrol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Mt Sinai Sch Med, Dept Med, New York, NY USA
关键词
podocyte biology; cultivation of differentiated podocytes; differentiation markers; proteinuric kidney diseases;
D O I
10.1038/sj.ki.5002291
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
Human genetic and in vivo animal studies have helped to define the critical importance of podocytes for kidney function in health and disease. However, as in any other research area, by default these approaches do not allow for mechanistic studies. Such mechanistic studies require the availability of cells grown ex vivo (i. e., in culture) with the ability to directly study mechanistic events and control the environment such that specific hypotheses can be tested. A seminal breakthrough came about a decade ago with the documentation of differentiation in culture of primary rat and human podocytes and the subsequent development of conditionally immortalized differentiated podocyte cell lines that allow deciphering the decisive steps of differentiation and function of `in vivo' podocytes. Although this paper is not intended to provide a comprehensive review of podocyte biology, nor their role in proteinuric renal diseases or progressive glomerulosclerosis, it will focus specifically on several aspects of podocytes in culture. In particular, we will discuss the scientific and research rationale and need for cultured podocytes, how podocyte cell-culture evolved, and how cultured podocytes are currently being used to uncover novel functions of podocytes that can then be validated in vivo in animal or human studies. In addition, we provide a detailed description of how to properly culture and characterize podocytes to avoid potential pitfalls.
引用
收藏
页码:26 / 36
页数:11
相关论文
共 100 条
[81]   THE TIGHT JUNCTION PROTEIN ZO-1 IS CONCENTRATED ALONG SLIT DIAPHRAGMS OF THE GLOMERULAR EPITHELIUM [J].
SCHNABEL, E ;
ANDERSON, JM ;
FARQUHAR, MG .
JOURNAL OF CELL BIOLOGY, 1990, 111 (03) :1255-1263
[82]  
Schwartz EJ, 2001, J AM SOC NEPHROL, V12, P1677, DOI 10.1681/ASN.V1281677
[83]   CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain [J].
Shih, NY ;
Li, J ;
Cotran, R ;
Mundel, P ;
Miner, JH ;
Shaw, AS .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (06) :2303-2308
[84]  
STRIKER GE, 1980, TRANSPL P, V12, P88
[85]   Glucose-induced reactive oxygen species cause apoptosis of podocytes and podocyte depletion at the onset of diabetic nephropathy [J].
Susztak, K ;
Raff, AC ;
Schiffer, M ;
Böttinger, EP .
DIABETES, 2006, 55 (01) :225-233
[86]  
TAKANO Y, 2007, AM J PHYSL RENAL PHY
[87]  
TAKEUCHI A, 1992, AM J PATHOL, V141, P107
[88]  
Teixeira VDC, 2005, KIDNEY INT, V67, P514
[89]   HUMAN GLOMERULAR EPITHELIAL-CELL PROTEOGLYCANS [J].
THOMAS, GJ ;
JENNER, L ;
MASON, RM ;
DAVIES, M .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 278 (01) :11-20
[90]   CD2AP/CIN85 balance determines receptor tyrosine kinase signaling response in podocytes [J].
Tossidou, Irini ;
Kardinal, Christian ;
Peters, Imke ;
Kriz, Wilhelm ;
Shaw, Andrey ;
Dikic, Ivan ;
Tkachuk, Sergej ;
Dumler, Inna ;
Haller, Hermann ;
Schiffer, Mario .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (10) :7457-7464