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@ARTICLE{Demaria:157096,
author = {M. C. Demaria and L. Yeung and R. Peeters and J. L. Wee and
M. Mihaljcic and E. L. Jones and Z. Nasa and F. Alderuccio
and P. Hall and B. C. Smith and K. J. Binger and G.
Hammerling$^*$ and H. F. Kwok and A. Newman and A. Ager and
A. van Spriel and M. J. Hickey and M. D. Wright},
title = {{T}etraspanin {CD}53 {P}romotes {L}ymphocyte
{R}ecirculation by {S}tabilizing {L}-{S}electin {S}urface
{E}xpression.},
journal = {iScience},
volume = {23},
number = {5},
issn = {2589-0042},
address = {St. Louis},
publisher = {Elsevier},
reportid = {DKFZ-2020-01387},
pages = {101104},
year = {2020},
abstract = {Tetraspanins regulate key processes in immune cells;
however, the function of the leukocyte-restricted
tetraspanin CD53 is unknown. Here we show that CD53 is
essential for lymphocyte recirculation. Lymph nodes of
Cd53-/- mice were smaller than those of wild-type mice due
to a marked reduction in B cells and a $50\%$ decrease in
T cells. This reduced cellularity reflected an inability of
Cd53-/- B and T cells to efficiently home to lymph nodes,
due to the near absence of L-selectin from Cd53-/- B cells
and reduced stability of L-selectin on Cd53-/- T cells.
Further analyses, including on human lymphocytes, showed
that CD53 stabilizes L-selectin surface expression and may
restrain L-selectin shedding via both ADAM17-dependent and
ADAM17-independent mechanisms. The disruption in lymphocyte
recirculation in Cd53-/- mice led to impaired immune
responses dependent on antigen delivery to lymph nodes.
Together these findings demonstrate an essential role for
CD53 in lymphocyte trafficking and immunity.},
cin = {D030},
ddc = {050},
cid = {I:(DE-He78)D030-20160331},
pnm = {314 - Tumor immunology (POF3-314)},
pid = {G:(DE-HGF)POF3-314},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32428859},
pmc = {pmc:PMC7232089},
doi = {10.1016/j.isci.2020.101104},
url = {https://inrepo02.dkfz.de/record/157096},
}