Raman microspectroscopy reveals unsaturation heterogeneity at the lipid droplet level and validates an in vitro model of bone marrow adipocyte subtypes

Published: 3 October 2022| Version 1 | DOI: 10.17632/wdm9gvz3bm.1
, Daniel Tavakol, Vasco Campos, Ludovic Duponchel,
, Guillaume Penel, Christophe Chauveau,


Bone marrow adipocytes (BMAds) constitute the most abundant stromal component of adult human BM. Two subtypes of BMAds have been described, the more labile regulated adipocytes (rBMAds) and the more stable constitutive adipocytes (cBMAds), which develop earlier and are more resilient to environmental and metabolic disruptions. In vivo, rBMAds are enriched in saturated fatty acids, contain smaller lipid droplets (LDs) and more readily provide hematopoietic support than their cBMAd counterparts. Mouse models have been used for BMAds research, but isolation of primary BMAds presents many challenges, and thus in vitro models remain the current standard to study nuances of adipocyte differentiation. No in vitro model has been described for the study of rBMAds/cBMAds. Here, we present an in vitro model of BM adipogenesis with differential rBMAd and cBMAd-like characteristics. We used OP9 BM stromal cells derived from a (C57BL/6xC3H)F2-op/op mouse, which have been extensively characterized as feeder layer in hematopoiesis research. We observed similar canonical adipogenesis transcriptional signatures for spontaneously-differentiated (sOP9) and induced (iOP9) cultures, while fatty acid composition and desaturase expression differed at the population level. To resolve differences at the single adipocyte level we show that Raman microspectroscopy presents a high-resolution method for studying adipogenesis in vitro in a label-free manner, with resolution to individual LDs in this model. We find sOP9 adipocytes have lower unsaturation ratios, smaller LDs and higher hematopoietic support than iOP9 adipocytes, thus functionally resembling rBMAds and cBMAds, respectively. Validation in human samples confirms a higher unsaturation ratio for lipids extracted from stable cBMAds (femoral head upon hip-replacement surgery) versus labile rBMAds (iliac crest after chemotherapy). Moreover, the 16:1/16:0 fatty acid unsaturation ratio, already shown to discriminate cBMAds from rBMAd in rabbit and rat marrow, was validated in both the OP9 model in vitro system and in human samples. We expect our model will be useful for cBMAd and rBMAd studies, particularly where isolation of primary BMAds is a limiting step.



High Performance Liquid Chromatography, Real-Time Polymerase Chain Reaction, Raman Microscopy