Mechanism of the process formation; podocytes vs. neurons
- 7 May 2002
- journal article
- research article
- Published by Wiley in Microscopy Research and Technique
- Vol. 57 (4) , 217-223
- https://doi.org/10.1002/jemt.10077
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. Microsc. Res. Tech. 57:217–223, 2002.Keywords
This publication has 79 references indexed in Scilit:
- Laminin-1 Activates Cdc42 in the Mechanism of Laminin-1-Mediated Neurite OutgrowthExperimental Cell Research, 2000
- Regulation of mouse podocyte process dynamics by protein tyrosine phosphatasesKidney International, 2000
- Novel Dendritic Kinesin Sorting Identified by Different Process Targeting of Two Related Kinesins: KIF21A and KIF21BThe Journal of cell biology, 1999
- Microtubules and Neuronal PolarityNeuron, 1999
- KIFC2 Is a Novel Neuron-Specific C-Terminal Type Kinesin Superfamily Motor for Dendritic Transport of Multivesicular Body-Like OrganellesNeuron, 1997
- Organization of microtubules in myelinating Schwann cellsJournal of Neurocytology, 1994
- The protein phosphatase inhibitor okadaic acid increases axonal neurofilaments and neurite caliber, and decreases axonal microtubules in NB2a/d1 CellsJournal of Neuroscience Research, 1993
- A plus-end-directed motor enzyme that moves antiparallel microtubules in vitro localizes to the interzone of mitotic spindlesNature, 1992
- Polarity orientation of microtubules in hippocampal neurons: uniformity in the axon and nonuniformity in the dendrite.Proceedings of the National Academy of Sciences, 1988
- Distribution of a matrix component of the midbody during the cell cycle in Chinese hamster ovary cellsThe Journal of cell biology, 1988