MarrowCellDLD: a microfluidic method for label-free retrieval of fragile bone marrow-derived cells.

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Serval ID
serval:BIB_EE628D166E3F
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
MarrowCellDLD: a microfluidic method for label-free retrieval of fragile bone marrow-derived cells.
Journal
Scientific reports
Author(s)
Porro G. (co-first), Sarkis R. (co-first), Obergozo C., Godot L., Amato F., Humbert M., Naveiras O. (co-last), Guiducci C. (co-last)
ISSN
2045-2322 (Electronic)
ISSN-L
2045-2322
Publication state
Published
Issued date
18/12/2023
Peer-reviewed
Oui
Volume
13
Number
1
Pages
22462
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
Functional bone marrow studies have focused primarily on hematopoietic progenitors, leaving limited knowledge about other fragile populations, such as bone marrow adipocytes (BMAds) and megakaryocytes. The isolation of these cells is challenging due to rupture susceptibility and large size. We introduce here a label-free cytometry microsystem, MarrowCellDLD, based on deterministic lateral displacement. MarrowCellDLD enables the isolation of large, fragile BM-derived cells based on intrinsic size properties while preserving their viability and functionality. Bone marrow adipocytes, obtained from mouse and human stromal line differentiation, as well as megakaryocytes, from primary human CD34+ hematopoietic stem and progenitor cells, were used for validation. Precise micrometer-range separation cutoffs were adapted for each cell type. Cells were sorted directly in culture media, without pre-labeling steps, and with real-time imaging for quality control. At least 10 <sup>6</sup> cells were retrieved intact per sorting round. Our method outperformed two FACS instruments in purity and yield, particularly for large cell size fractions. MarrowCellDLD represents a non-destructive sorting tool for large, fragile BM-derived cells, facilitating the separation of pure populations of BMAds and megakaryocytes to further investigate their physiological and pathological roles.
Keywords
Humans, Mice, Animals, Hematopoietic Stem Cells, Bone Marrow, Microfluidics, Cell Separation/methods, Megakaryocytes, Antigens, CD34, Bone Marrow Cells, Cell Differentiation, Flow Cytometry
Pubmed
Open Access
Yes
Create date
21/12/2023 16:18
Last modification date
22/03/2024 8:36
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