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Selective blocking of clathrin-mediated endocytosis by RNA interference: epsin as target protein

Davy Vanden Broeck UGent and Marc JS De Wolf (2006) BIOTECHNIQUES. 41(4). p.475-484
abstract
Epsin is an essential accessory protein exclusively implicated in clathrin-mediated endocytosis and therefore an ideal target to study involvement of this entry route in the uptake of bioligands. The technique of RNA interference (RNAi) was exploited to generate a cell line constitutively silencing epsin expression in a sequence-specific manner In these Caco-2(eps-) cells, quantitative reverse transcription PCR (RT-PCR) revealed a severe depletion of the epsin messenger RNA (mRNA) level in cells, reaching a factor > 10(6). The reduction at the mRNA level in the Caco-2(eps-) cells was paralleled by a decrease of 75% at the protein level. In order to evaluate transfection effects at the functional level, uptake of transferrin and epidermal growth factor (EGF) in transfected Caco-2(eps-) and control cells was evaluated. In control cells, respectively, approximately 72% of transferrin and approximately 66% of EGF(.) were internalized, whereas in Caco-2(eps-) cells only approximately 25% of transferrin and approximately 34% of EGF was taken up, Confirming that in the transfected cells, endocytosis via coated pits was prominently compromised. The reduced uptake was not the result of an inhibition of transferrin recycling. The effects of direct treatment with chlorpromazine on Caco-2 cells, also monitored from the degree of transferrin internalization, were compared with those elicited by RNAi.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
EH-DOMAIN, BINDING, ENTH DOMAIN, COATED PITS, CELLS, EXPRESSION, CHOLESTEROL, INHIBITION, INTERACTS, LATTICES
journal title
BIOTECHNIQUES
Biotechniques
volume
41
issue
4
pages
475 - 484
Web of Science type
Article
Web of Science id
000241269500027
JCR category
BIOCHEMICAL RESEARCH METHODS
JCR impact factor
2.462 (2006)
JCR rank
28/56 (2006)
JCR quartile
2 (2006)
ISSN
0736-6205
DOI
10.2144/000112265
language
English
UGent publication?
no
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
2150359
handle
http://hdl.handle.net/1854/LU-2150359
date created
2012-06-13 14:50:12
date last changed
2016-12-19 15:42:06
@article{2150359,
  abstract     = {Epsin is an essential accessory protein exclusively implicated in clathrin-mediated endocytosis and therefore an ideal target to study involvement of this entry route in the uptake of bioligands. The technique of RNA interference (RNAi) was exploited to generate a cell line constitutively silencing epsin expression in a sequence-specific manner In these Caco-2(eps-) cells, quantitative reverse transcription PCR (RT-PCR) revealed a severe depletion of the epsin messenger RNA (mRNA) level in cells, reaching a factor {\textrangle} 10(6). The reduction at the mRNA level in the Caco-2(eps-) cells was paralleled by a decrease of 75\% at the protein level. In order to evaluate transfection effects at the functional level, uptake of transferrin and epidermal growth factor (EGF) in transfected Caco-2(eps-) and control cells was evaluated. In control cells, respectively, approximately 72\% of transferrin and approximately 66\% of EGF(.) were internalized, whereas in Caco-2(eps-) cells only approximately 25\% of transferrin and approximately 34\% of EGF was taken up, Confirming that in the transfected cells, endocytosis via coated pits was prominently compromised. The reduced uptake was not the result of an inhibition of transferrin recycling. The effects of direct treatment with chlorpromazine on Caco-2 cells, also monitored from the degree of transferrin internalization, were compared with those elicited by RNAi.},
  author       = {Vanden Broeck, Davy and De Wolf, Marc JS},
  issn         = {0736-6205},
  journal      = {BIOTECHNIQUES},
  keyword      = {EH-DOMAIN,BINDING,ENTH DOMAIN,COATED PITS,CELLS,EXPRESSION,CHOLESTEROL,INHIBITION,INTERACTS,LATTICES},
  language     = {eng},
  number       = {4},
  pages        = {475--484},
  title        = {Selective blocking of clathrin-mediated endocytosis by RNA interference: epsin as target protein},
  url          = {http://dx.doi.org/10.2144/000112265},
  volume       = {41},
  year         = {2006},
}

Chicago
Vanden Broeck, Davy, and Marc JS De Wolf. 2006. “Selective Blocking of Clathrin-mediated Endocytosis by RNA Interference: Epsin as Target Protein.” Biotechniques 41 (4): 475–484.
APA
Vanden Broeck, D., & De Wolf, M. J. (2006). Selective blocking of clathrin-mediated endocytosis by RNA interference: epsin as target protein. BIOTECHNIQUES, 41(4), 475–484.
Vancouver
1.
Vanden Broeck D, De Wolf MJ. Selective blocking of clathrin-mediated endocytosis by RNA interference: epsin as target protein. BIOTECHNIQUES. 2006;41(4):475–84.
MLA
Vanden Broeck, Davy, and Marc JS De Wolf. “Selective Blocking of Clathrin-mediated Endocytosis by RNA Interference: Epsin as Target Protein.” BIOTECHNIQUES 41.4 (2006): 475–484. Print.