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Analysis of extracellular matrix proteins produced by cultured cells

Turoverova, L.V. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
Khotin, M.G. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
Yudintseva, N.M. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
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Magnusson, Karl-Eric (author)
Linköpings universitet,Medicinsk mikrobiologi,Hälsouniversitetet
Blinova, M.I. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
Pinaev, G.P. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
Tentler, D.G. (author)
Institute of Cytology RAS, St. Petersburg, Russian Federation
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Institute of Cytology RAS, St Petersburg, Russian Federation Medicinsk mikrobiologi (creator_code:org_t)
St Petersburg, Russian Federation : Sankt-Peterburgskaya Izdatel'skaya Firma Nauka, 2009
2009
Russian.
In: Tsitologiya. - St Petersburg, Russian Federation : Sankt-Peterburgskaya Izdatel'skaya Firma Nauka. - 0041-3771. ; 51:8, s. 691-696
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Extracellular matrix (ECM) is a highly organized multimolecular structure essential for vital function of any organism. Although a lot of data on the extracellular matrix components has been accumulated, an isolation of the entire set of these proteins still remains to be a complex procedure since ECM contains fibrillar proteins and proteoglycans, which form multidomain net-like structures. In the presented study, we developed a method for isolation of ECM proteins from cell cultures. Human epidermoid carcinoma cells A431 and fibroblasts obtained from normal and scar human skin were used. We showed that EDTA solution removed cells from culture plates without destroying the cell membrane. Following treatment of remaining ECM proteins with acetic acid in order to dissociate collagen fibrils significantly improved fractioning of ECM proteins. Extraction of the remained proteins from culture plate surface was preformed using a buffer developed on the basis of Laemmli probe buffer. With this method, we isolated ECM proteins synthesized by culturing cells and suitable for a future analysis by SDS PAGE and two-dimentional electrophoresis as well as for identification of individual proteins by mass-spectrometry. This study may allow comparing protein contents of ECMs isolated from different sources, and elucidate influences of various proteins on the protein and the properties of extracellular matrix of investigated cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Keyword

Collagen; Extracellular matrix; Fibroblasts; Fibronectin
MEDICINE
MEDICIN

Publication and Content Type

ref (subject category)
art (subject category)

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