Please note that eDoc will be permanently shut down in the first quarter of 2021!      Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für medizinische Forschung     Collection: Abteilung Molekulare Zellforschung     Display Documents



ID: 568804.0, MPI für medizinische Forschung / Abteilung Molekulare Zellforschung
The membrane fusion events in degranulating guinea pig eosinophils
Translation of Title:The membrane fusion events in degranulating guinea pig eosinophils
Authors:Lindau, Manfred; Nüße, Oliver; Bennett, J.; Cromwell, O.
Language:English
Date of Publication (YYYY-MM-DD):1993-01-01
Title of Journal:Journal of Cell Science
Journal Abbrev.:J. Cell Sci.
Volume:104
Issue / Number:1
Start Page:203
End Page:210
Review Status:Peer-review
Audience:Experts Only
Intended Educational Use:No
Abstract / Description:We have investigated the granule fusion events associated with exocytosis in degranulating peritoneal guinea pig eosinophils by time−resolved patch−clamp capacitance measurements using the phase detector technique. Intracellular stimulation with micromolar calcium and GTP gamma S induces a 2− to 3−fold capacitance increase. The main phase of the capacitance increase occurs after a delay of 2−7 minutes and is composed of well−resolved capacitance steps. The number of steps is very close to the number of crystalloid granules contained in a resting cell and the step size distribution with a peak at 9 fF is in excellent agreement with the granule size distribution determined by electron microscopy. The individual granules thus fuse sequentially with the plasma membrane. The stepwise capacitance increase is frequently preceded by an apparently continuous capacitance increase which consists of steps smaller than 4 fF, indicating exocytosis of small vesicles as distinct from crystalloid−containing granules. In some cases the time course of the opening of individual fusion pores could be recorded, and this revealed metastable conductance states below 300 pS but random fluctuations at higher conductance levels. This behaviour suggests that the small fusion pore might be a protein structure similar to an ion channel, which becomes a continuously variable lipid pore at higher conductances. In some cells a significant capacitance decrease was observed which is apparently continuous, suggesting a process of membrane uptake by endocytosis of small vesicles
Last Change of the Resource (YYYY-MM-DD):--
External Publication Status:published
Document Type:Article
Communicated by:Wulf Kaiser
Affiliations:MPI für medizinische Forschung/Abteilung Molekulare Zellforschung
Identifiers:LOCALID:7013
URI:http%3A%2F%2Fjcs.biologists.org%2Fcgi%2Freprint%2F...
URI:http%3A%2F%2Fjcs.biologists.org%2Fcgi%2Fcontent%2F...
Full Text:
Sorry, no privileges
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.