Soluble HLA-G generated by proteolytic shedding inhibits NK-mediated cell lysis
Biochemical and Biophysical Research Communications, ISSN: 0006-291X, Vol: 313, Issue: 3, Page: 606-611
2004
- 156Citations
- 57Captures
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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
- Citations156
- Citation Indexes156
- 156
- CrossRef128
- Captures57
- Readers57
- 57
Article Description
In contrast to the classical HLA class Ia molecules, the nonclassical HLA-G primary transcript is alternatively spliced to generate several mRNAs that encode four membrane-bound and three soluble isoforms. This study demonstrated that the soluble form of HLA-G can also be generated by metalloproteinase-dependent shedding at post-translational level. These soluble HLA-G1 molecules generated by the cleavage of membrane-bound HLA-G1 associate with β2-microglobulin and contain bound peptides that are stable at physiological conditions. This report further showed that the soluble HLA-G1 is able to protect HLA class I-negative K562 cells from NK lysis, suggesting that soluble HLA-G could act as an immunoregulator in NK cell recognition and possibly in other immune responses.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0006291X03025610; http://dx.doi.org/10.1016/j.bbrc.2003.11.153; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0346433828&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/14697234; https://linkinghub.elsevier.com/retrieve/pii/S0006291X03025610; https://dx.doi.org/10.1016/j.bbrc.2003.11.153
Elsevier BV
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