TY - JOUR
T1 - LGR6 marks nephron progenitor cells
AU - van Ineveld, Ravian L
AU - Margaritis, Thanasis
AU - Kooiman, Berend A P
AU - Groenveld, Femke
AU - Ariese, Hendrikus C R
AU - Lijnzaad, Philip
AU - Johnson, Hannah R
AU - Korving, Jeroen
AU - Wehrens, Ellen J
AU - Holstege, Frank
AU - van Rheenen, Jacco
AU - Drost, Jarno
AU - Rios, Anne C
AU - Bos, Frank L
N1 - © 2021 The Authors. Developmental Dynamics published by Wiley Periodicals LLC on behalf of American Association of Anatomists.
PY - 2021/11
Y1 - 2021/11
N2 - BACKGROUND: Nephron progenitor cells (NPCs) undergo a stepwise process to generate all mature nephron structures. Mesenchymal to epithelial transition (MET) is considered a multistep process of NPC differentiation to ensure progressive establishment of new nephrons. However, despite this important role, to date, no marker for NPCs undergoing MET in the nephron exists.RESULTS: Here, we identify LGR6 as a NPC marker, expressed in very early cap mesenchyme, pre-tubular aggregates, renal vesicles, and in segments of S-shaped bodies, following the trajectory of MET. By using a lineage tracing approach in embryonic explants in combination with confocal imaging and single-cell RNA sequencing, we provide evidence for the multiple fates of LGR6+ cells during embryonic nephrogenesis. Moreover, by using long-term in vivo lineage tracing, we show that postnatal LGR6+ cells are capable of generating the multiple lineages of the nephrons.CONCLUSIONS: Given the profound early mesenchymal expression and MET signature of LGR6+ cells, together with the lineage tracing of mesenchymal LGR6+ cells, we conclude that LGR6+ cells contribute to all nephrogenic segments by undergoing MET. LGR6+ cells can therefore be considered an early committed NPC population during embryonic and postnatal nephrogenesis with potential regenerative capability.
AB - BACKGROUND: Nephron progenitor cells (NPCs) undergo a stepwise process to generate all mature nephron structures. Mesenchymal to epithelial transition (MET) is considered a multistep process of NPC differentiation to ensure progressive establishment of new nephrons. However, despite this important role, to date, no marker for NPCs undergoing MET in the nephron exists.RESULTS: Here, we identify LGR6 as a NPC marker, expressed in very early cap mesenchyme, pre-tubular aggregates, renal vesicles, and in segments of S-shaped bodies, following the trajectory of MET. By using a lineage tracing approach in embryonic explants in combination with confocal imaging and single-cell RNA sequencing, we provide evidence for the multiple fates of LGR6+ cells during embryonic nephrogenesis. Moreover, by using long-term in vivo lineage tracing, we show that postnatal LGR6+ cells are capable of generating the multiple lineages of the nephrons.CONCLUSIONS: Given the profound early mesenchymal expression and MET signature of LGR6+ cells, together with the lineage tracing of mesenchymal LGR6+ cells, we conclude that LGR6+ cells contribute to all nephrogenic segments by undergoing MET. LGR6+ cells can therefore be considered an early committed NPC population during embryonic and postnatal nephrogenesis with potential regenerative capability.
KW - Cell Differentiation
KW - Mesoderm
KW - Nephrons
KW - Organogenesis/genetics
KW - Stem Cells
UR - http://www.scopus.com/inward/record.url?scp=85104894769&partnerID=8YFLogxK
U2 - 10.1002/dvdy.346
DO - 10.1002/dvdy.346
M3 - Article
C2 - 33848015
SN - 1058-8388
VL - 250
SP - 1568
EP - 1583
JO - Developmental dynamics : an official publication of the American Association of Anatomists
JF - Developmental dynamics : an official publication of the American Association of Anatomists
IS - 11
ER -