Literature DB >> 12012387

Mechanism of the process formation; podocytes vs. neurons.

Naoto Kobayashi1.   

Abstract

In this review article we discuss the common mechanism for cellular process formation. Besides the podocyte, the mechanism of process formation, including cytoskeletal organization and signal transduction, etc., has been studied using neurons and glias as model systems. There has been an accumulation of data showing common cell biological features of the podocyte and the neuron: 1) Both cells possess long and short cell processes equipped with highly organized cytoskeletal systems; 2) Both show cytoskeletal segregation; microtubules (MTs) and intermediate filaments (IFs) in podocyte primary processes and in neurites, while actin filaments (AFs) are abundant in podocyte foot processes in neuronal synaptic regions; 3) In both cells, process formation is mechanically dependent on MTs, whose assembly is regulated by various microtubule- associated proteins (MAPs); 4) In both cells, process formation is positively regulated by PP2A, a Ser/Thr protein phosphatase; 5) In both cells, process formation is accelerated by laminin, an extracellular matrix protein. In addition, recent data from our and other laboratories have shown that podocyte processes share many features with neuronal dendrites: 1) Podocyte processes and neuronal dendrites possess MTs with mixed polarity, namely, plus-end-distal and minus-end-distal MTs coexist in these processes; 2) To establish the mixed polarity of MTs, both express CHO1/MKLP1, a kinesin-related motor protein, and when its expression is inhibited formation of both podocyte processes and neuronal dendrites is abolished; 3) The elongation of both podocyte processes and neuronal dendrites is supported by rab8-regulated basolateral-type membrane transport; 4) Both podocyte processes and neuronal dendrites express synaptopodin, an actin-associated protein, in a development-dependent manner; interestingly, in both cells, synaptopodin is localized not in the main shaft of processes but in thin short projections from the main shaft. We propose that the podocyte process and the neuronal dendrite share many features, while the neuronal axon should be thought of as an exceptionally differentiated cellular process. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12012387     DOI: 10.1002/jemt.10077

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  28 in total

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5.  Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking.

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Review 6.  APOL1 Kidney Disease Risk Variants: An Evolving Landscape.

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8.  Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.

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Journal:  Pediatr Nephrol       Date:  2008-07-02       Impact factor: 3.714

9.  Cyclin-dependent kinase 5 is a regulator of podocyte differentiation, proliferation, and morphology.

Authors:  Sian V Griffin; Keiju Hiromura; Jeffrey Pippin; Arndt T Petermann; Mary J Blonski; Ron Krofft; Satoru Takahashi; Ashok B Kulkarni; Stuart J Shankland
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10.  Densin and beta-catenin form a complex and co-localize in cultured podocyte cell junctions.

Authors:  Eija Heikkilä; Mervi Ristola; Karlhans Endlich; Sanna Lehtonen; Markus Lassila; Marika Havana; Nicole Endlich; Harry Holthöfer
Journal:  Mol Cell Biochem       Date:  2007-06-21       Impact factor: 3.396

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