Glomerular podocytes possess the synaptic vesicle molecule Rab3A and its specific effector rabphilin-3a

被引:49
作者
Rastaldi, MP
Armelloni, S
Berra, S
Li, M
Pesaresi, M
Poczewski, H
Langer, B
Kerjaschki, D
Henger, A
Blattner, SM
Kretzler, M
Wanke, R
D'Amico, G
机构
[1] San Carlo Borromeo Hosp, Assoc Nuova Nefrol, Renal Immunopathol Lab, I-20153 Milan, Italy
[2] Univ Vienna, Inst Clin Pathol, Vienna, Austria
[3] Univ Munich, Klin Biochem, Munich, Germany
[4] Univ Munich, Med Poliklin, Munich, Germany
[5] Univ Munich, Inst Vet Pathol, Munich, Germany
关键词
D O I
10.1016/S0002-9440(10)63449-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Several recent studies have focused on similarities between glomerular podocytes and neurons because the two cells share a specialized cytoskeletal organization and several expression-restricted proteins, such as nephrin and synaptopodin. in neurons, the small guanosine triphosphatase Rab3A and its effector rabphilin-3A form a complex required for the correct docking of synaptic vesicles to their target membrane. Because rabphilin-3A binds in neurons to cytoskeletal proteins also important for podocyte homeostasis, and the complex rabphilin-3A-Rab3A has been demonstrated in neurons and neuroendocrine cells, the aim of our work was to investigate their possible expression and regulation in podocytes. Normal kidneys from mouse, rat, and human were studied by immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction to evaluate the expression of Rab3A and rabphilin-3A. Double-staining immunohistochemistry and immunogold electron microscopy were then used to precisely localize the two proteins at the cellular and subcellular levels. Rab-3A and rabphilin-3A regulations in disease were then analyzed in growth hormone-transgenic mice, a well established model of focal and segmental glomerulosclerosis, and in human biopsies from proteinuric patients. Our results demonstrated that rabphilin-3A and Rab3A are present in normal mouse, rat, and human kidneys, with an exclusively glomerular expression and a comma-like pattern of positivity along the glomerular capillary wall, suggestive for podocyte staining. Co-localization of both molecules with synaptopodin confirmed their presence in podocytes. By immuno-gold electron microscopy both proteins were found around vesicles contained in podocyte foot processes. Their expression was increased in growth hormone-transgenic mice compared to their wild-type counterpart, and in a subset of biopsies from proteinuric patients. our data, demonstrating the presence of two synaptic proteins in podocytes, further supports similarities between cytoskeletal and vesicular organization of podocytes and neurons. The altered expression observed in mouse and human proteinuric diseases suggests a possible role for these molecules in glomerulopathies.
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页码:889 / 899
页数:11
相关论文
共 26 条
[1]  
ADLER S, 1997, GLOMERULAR EPITHELIA, P655
[2]  
Araki N, 2000, J CELL SCI, V113, P3329
[3]   Rabphilin-3A: A multifunctional regulator of synaptic vesicle traffic [J].
Burns, ME ;
Sasaki, T ;
Takai, Y ;
Augustine, GJ .
JOURNAL OF GENERAL PHYSIOLOGY, 1998, 111 (02) :243-255
[4]   Evidence for an alpha-granular pool of the cytoskeletal protein alpha-actinin in human platelets that redistributes with the adhesive glycoprotein thrombospondin-1 during the exocytotic process [J].
Dubernard, V ;
Arbeille, BB ;
Lemesle, MB ;
Legrand, C .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (10) :2293-2305
[5]  
FISCHER V, 1990, P NATL ACAD SCI USA, V87, P1988
[6]   Amino acid transport in podocytes [J].
Gloy, J ;
Reitinger, S ;
Fischer, KG ;
Schreiber, R ;
Boucherot, A ;
Kunzelmann, K ;
Mundel, P ;
Pavenstädt, H .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (06) :F999-F1005
[7]   Regulation of membrane trafficking: Structural insights from a Rab/effector complex [J].
Gonzalez, L ;
Scheller, RH .
CELL, 1999, 96 (06) :755-758
[8]  
HOLZ RW, 1994, J BIOL CHEM, V269, P10229
[9]   Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis [J].
Kaplan, JM ;
Kim, SH ;
North, KN ;
Rennke, H ;
Correia, LA ;
Tong, HQ ;
Mathis, BJ ;
Rodríguez-Pérez, JC ;
Allen, PG ;
Beggs, AH ;
Pollak, MR .
NATURE GENETICS, 2000, 24 (03) :251-256
[10]   Physical and functional interaction of rabphilin-3A with alpha-actinin [J].
Kato, M ;
Sasaki, T ;
Ohya, T ;
Nakanishi, H ;
Nishioka, H ;
Imamura, M ;
Takai, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :31775-31778