[Comparision of intracellular localization and recycling route of mouse nepmucin and CD31 in endothelial cells].

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi

Division of Clinical Immunology, Department of Laboratory Medicine, West China Hospital, Chengdu 610041, China.

Published: December 2011

Aim: To compare the localization and recycling between nepmucin and CD31 molecules on transfected endothelial cells, and attempted to clarify the recycling mechanisms of nepmucin in endothelial cells.

Methods: Recycling assay and internalization assay were employed to compare the localization and recycling pathway of nepmucin and CD31. The internalized and recycling nepmucin and CD31 molecules on transfected endothelial cells were double or single stained with specific fluorchrome-labeled monoclonal antibodies against nepmucin (Alexa Fluor 488-ZAQ5) and/or CD31 (Alexa Fluor 488-anti-CD31 or Alexa Fluor 594-anti-CD31), then observed under confocal microscopy.

Results: Mouse nepmucin underwent intracellular recycling like CD31, but which recycling rate was significantly lower. The CD31 and nepmucin molecules showed largely distinct localization in endothelial cells. CD31 was found mainly on the cell surface, while nepmucin was found predominantly in the deep area of cytoplasm and partly on the cell membrane.

Conclusion: The distribution of mouse nepmucin in endothelial cells are different from CD31. Nepmucin underwent intracellular recycling like CD31 but employed different mechanisms.

Download full-text PDF

Source

Publication Analysis

Top Keywords

nepmucin cd31
16
endothelial cells
16
localization recycling
12
mouse nepmucin
12
alexa fluor
12
nepmucin
11
cd31
10
recycling
9
compare localization
8
recycling nepmucin
8

Similar Publications

[Comparision of intracellular localization and recycling route of mouse nepmucin and CD31 in endothelial cells].

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi

December 2011

Division of Clinical Immunology, Department of Laboratory Medicine, West China Hospital, Chengdu 610041, China.

Aim: To compare the localization and recycling between nepmucin and CD31 molecules on transfected endothelial cells, and attempted to clarify the recycling mechanisms of nepmucin in endothelial cells.

Methods: Recycling assay and internalization assay were employed to compare the localization and recycling pathway of nepmucin and CD31. The internalized and recycling nepmucin and CD31 molecules on transfected endothelial cells were double or single stained with specific fluorchrome-labeled monoclonal antibodies against nepmucin (Alexa Fluor 488-ZAQ5) and/or CD31 (Alexa Fluor 488-anti-CD31 or Alexa Fluor 594-anti-CD31), then observed under confocal microscopy.

View Article and Find Full Text PDF

Nepmucin/CLM-9 is an Ig domain-containing sialomucin expressed in vascular endothelial cells. Here we show that, like CD31, nepmucin was localized to interendothelial contacts and to vesicle-like structures along the cell border and underwent intracellular recycling. Functional analyses showed that nepmucin mediated homotypic and heterotypic cell adhesion via its Ig domain.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!