TY - JOUR
T1 - Human lymph node fibroblastic reticular cells maintain heterogeneous characteristics in culture
AU - Roet, Janna E.G.
AU - Morrison, Andrew I.
AU - Mikula, Aleksandra M.
AU - de Kok, Michael
AU - Panocha, Daphne
AU - Roest, Henk P.
AU - van der Laan, Luc J.W.
AU - de Winde, Charlotte M.
AU - Mebius, Reina E.
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/7/19
Y1 - 2024/7/19
N2 - Fibroblastic reticular cells (FRCs) are mesenchymal stromal cells in human lymph nodes (LNs) playing a pivotal role in adaptive immunity. Several FRC subsets have been identified, yet it remains to be elucidated if their heterogeneity is maintained upon culture. Here, we established a protocol to preserve and culture FRCs from human LNs and characterized their phenotypic profile in fresh LN suspensions and upon culture using multispectral flow cytometry. We found nine FRC subsets in fresh human LNs, independent of donor, of which four persisted in culture throughout several passages. Interestingly, the historically FRC-defining marker podoplanin (PDPN) was not present on all FRC subsets. Therefore, we propose that CD45negCD31neg human FRCs are not restricted by PDPN expression, as we found CD90, BST1, and CD146/MCAM to be more widely expressed. Together, our data provide insight into FRC heterogeneity in human LNs, enabling further investigation into the function of individual FRC subsets.
AB - Fibroblastic reticular cells (FRCs) are mesenchymal stromal cells in human lymph nodes (LNs) playing a pivotal role in adaptive immunity. Several FRC subsets have been identified, yet it remains to be elucidated if their heterogeneity is maintained upon culture. Here, we established a protocol to preserve and culture FRCs from human LNs and characterized their phenotypic profile in fresh LN suspensions and upon culture using multispectral flow cytometry. We found nine FRC subsets in fresh human LNs, independent of donor, of which four persisted in culture throughout several passages. Interestingly, the historically FRC-defining marker podoplanin (PDPN) was not present on all FRC subsets. Therefore, we propose that CD45negCD31neg human FRCs are not restricted by PDPN expression, as we found CD90, BST1, and CD146/MCAM to be more widely expressed. Together, our data provide insight into FRC heterogeneity in human LNs, enabling further investigation into the function of individual FRC subsets.
UR - http://www.scopus.com/inward/record.url?scp=85195866557&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2024.110179
DO - 10.1016/j.isci.2024.110179
M3 - Article
C2 - 38989462
AN - SCOPUS:85195866557
SN - 2589-0042
VL - 27
JO - iScience
JF - iScience
IS - 7
M1 - 110179
ER -