TY - JOUR
T1 - Spatiotemporal dynamics of fetal liver hematopoietic niches
AU - Mesquita Peixoto, Márcia
AU - Soares-Da-silva, Francisca
AU - Bonnet, Valentin
AU - Zhou, Yanping
AU - Ronteix, Gustave
AU - Santos, Rita Faria
AU - Mailhe, Marie Pierre
AU - Nogueira, Gonçalo
AU - Feng, Xing
AU - Pereira, João Pedro
AU - Azzoni, Emanuele
AU - Anselmi, Giorgio
AU - de Bruijn, Marella F.T.R.
AU - Perkins, Archibald
AU - Baroud, Charles N.
AU - Pinto-Do-ó, Perpétua
AU - Cumano, Ana
N1 - Publisher Copyright:
© 2025 Mesquita Peixoto et al.
PY - 2025/2/3
Y1 - 2025/2/3
N2 - Embryonic hematopoietic cells develop in the fetal liver (FL), surrounded by diverse non-hematopoietic stromal cells. However, the spatial organization and cytokine production patterns of the stroma during FL development remain poorly understood. Here, we characterized and mapped the hematopoietic and stromal cell populations at early (E12.5–14.5) FL stages, revealing that while hepatoblasts were the primary source of hematopoietic growth factors, other stromal cells—including mesenchymal, mesothelial, and endothelial cells—also contributed to this signaling network. Using a dedicated image analysis pipeline, we quantified cell distances to tissue structures and defined neighbor relationships, uncovering that different hematopoietic progenitors exhibit distinct preferences for neighboring stromal cells and show developmental changes in spatial distribution. Notably, our data suggest that the sub-mesothelium region plays a prominent role in early fetal hematopoiesis. This approach offers a valuable tool for studying complex cellular interactions in biological systems, providing new insights into hematopoietic niche organization during development.
AB - Embryonic hematopoietic cells develop in the fetal liver (FL), surrounded by diverse non-hematopoietic stromal cells. However, the spatial organization and cytokine production patterns of the stroma during FL development remain poorly understood. Here, we characterized and mapped the hematopoietic and stromal cell populations at early (E12.5–14.5) FL stages, revealing that while hepatoblasts were the primary source of hematopoietic growth factors, other stromal cells—including mesenchymal, mesothelial, and endothelial cells—also contributed to this signaling network. Using a dedicated image analysis pipeline, we quantified cell distances to tissue structures and defined neighbor relationships, uncovering that different hematopoietic progenitors exhibit distinct preferences for neighboring stromal cells and show developmental changes in spatial distribution. Notably, our data suggest that the sub-mesothelium region plays a prominent role in early fetal hematopoiesis. This approach offers a valuable tool for studying complex cellular interactions in biological systems, providing new insights into hematopoietic niche organization during development.
UR - https://www.scopus.com/pages/publications/85215080690
U2 - 10.1084/jem.20240592
DO - 10.1084/jem.20240592
M3 - Article
C2 - 39775824
AN - SCOPUS:85215080690
SN - 1540-9538
VL - 222
JO - The Journal of experimental medicine
JF - The Journal of experimental medicine
IS - 2
M1 - e20240592
ER -