Altered configuration of Gc on the plasma membrane of transformed and malignant human B lymphocytes
Clinical Immunology and Immunopathology, ISSN: 0090-1229, Vol: 37, Issue: 2, Page: 191-202
1985
- 9Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations9
- Citation Indexes9
- CrossRef8
- Captures5
- Readers5
Article Description
Normal human peripheral blood B cells exhibit strong membrane fluorescence for Gc (vitamin D-binding protein), and this protein can form a close spatial relationship with integral membrane immunoglobulin (mIg) with evidence of codistribution in the lipid bilayer. In contrast, fluorescence for both Gc and mIg has been found in this study to be weak or absent in several B lymphoblastoid cell lines and in chronic lymphocytic leukemia B cells. Moreover, the comobility of these components, where detectable, was also impaired. In abnormal B cells, the intensity of membrane fluorescence for Gc was substantially increased after crosslinking of mIg with antibody, and the latter was also associated with increased specific radioiodination of Gc by lactoperioxidase. These results indicate that Gc can apparently become displaced under certain circumstances within or through the lipid bilayer. The altered content or membrane topography of Gc in such abnormal B cells might be associated with impaired expression and mobility of mIg.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0090122985901503; http://dx.doi.org/10.1016/0090-1229(85)90150-3; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84886641434&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/2994927; https://linkinghub.elsevier.com/retrieve/pii/0090122985901503; http://dx.doi.org/10.1016/0090-1229%2885%2990150-3; https://dx.doi.org/10.1016/0090-1229%2885%2990150-3
Elsevier BV
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