Synaptopodin: An Actin-associated Protein in Telencephalic Dendrites and Renal Podocytes
Open Access
- 6 October 1997
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 139 (1) , 193-204
- https://doi.org/10.1083/jcb.139.1.193
Abstract
A microneedle puncture of the fibroblast or sea urchin egg surface rapidly evokes a localized exocytotic reaction that may be required for the rapid resealing that follows this breach in plasma membrane integrity (Steinhardt, R.A,. G. Bi, and J.M. Alderton. 1994. Science (Wash. DC). 263:390–393). How this exocytotic reaction facilitates the resealing process is unknown. We found that starfish oocytes and sea urchin eggs rapidly reseal much larger disruptions than those produced with a microneedle. When an ∼40 by 10 μm surface patch was torn off, entry of fluorescein stachyose (FS; 1,000 mol wt) or fluorescein dextran (FDx; 10,000 mol wt) from extracellular sea water (SW) was not detected by confocal microscopy. Moreover, only a brief (∼5–10 s) rise in cytosolic Ca2+ was detected at the wound site. Several lines of evidence indicate that intracellular membranes are the primary source of the membrane recruited for this massive resealing event. When we injected FS-containing SW deep into the cells, a vesicle formed immediately, entrapping within its confines most of the FS. DiI staining and EM confirmed that the barrier delimiting injected SW was a membrane bilayer. The threshold for vesicle formation was ∼3 mM Ca2+ (SW is ∼10 mM Ca2+). The capacity of intracellular membranes for sealing off SW was further demonstrated by extruding egg cytoplasm from a micropipet into SW. A boundary immediately formed around such cytoplasm, entrapping FDx or FS dissolved in it. This entrapment did not occur in Ca2+-free SW (CFSW). When egg cytoplasm stratified by centrifugation was exposed to SW, only the yolk platelet–rich domain formed a membrane, suggesting that the yolk platelet is a critical element in this response and that the ER is not required. We propose that plasma membrane disruption evokes Ca2+ regulated vesicle–vesicle (including endocytic compartments but possibly excluding ER) fusion reactions. The function in resealing of this cytoplasmic fusion reaction is to form a replacement bilayer patch. This patch is added to the discontinuous surface bilayer by exocytotic fusion events.Keywords
This publication has 46 references indexed in Scilit:
- Prominent Dendritic Localization in Forebrain Neurons of a Novel mRNA and Its Product, DendrinMolecular and Cellular Neuroscience, 1997
- Synaptic proteins and the assembly of synaptic junctionsTrends in Cell Biology, 1996
- Towards prediction of cognate complexes between the WW domain and proline‐rich ligandsFEBS Letters, 1996
- Postsynaptic Mechanisms for Bidirectional Control of MAP2 Phosphorylation by Glutamate ReceptorsNeuron, 1996
- Cell type-specific desmosomal plaque proteins of the plakoglobin family: plakophilin 1 (band 6 protein)Differentiation, 1995
- The WW domain: a signalling site in dystrophin?Trends in Biochemical Sciences, 1994
- The postsynaptic densityCurrent Opinion in Neurobiology, 1993
- Calcium-induced actin depolymerization reduces NMDA channel activityPublished by Elsevier ,1993
- Podocytes in glomerulus of rat kidney express a characteristic 44 KD protein.Journal of Histochemistry & Cytochemistry, 1991
- Fractionation of Brain Microtubule‐Associated ProteinsEuropean Journal of Biochemistry, 1978