Evidence map›Paper›PMID 38105340›Full record

ArticleScientific reports2023

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

Gloria Porro, Rita Sarkis, Clara Obergozo, Lucie Godot, Francesco Amato, Magali Humbert, Olaia Naveiras, Carlotta Guiducci

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Gloria Porro *Laboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland. gloria.porro@epfl.ch.
Rita Sarkis *Laboratory of Regenerative Hematopoiesis, Université de Lausanne (UNIL), Lausanne, Switzerland. rita.sarkis@unil.ch.
Clara ObergozoLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Lucie GodotLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Francesco AmatoLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Magali HumbertLaboratory of Regenerative Hematopoiesis, Université de Lausanne (UNIL), Lausanne, Switzerland.
Olaia NaveirasLaboratory of Regenerative Hematopoiesis, Université de Lausanne (UNIL), Lausanne, Switzerland. Olaia.naveiras@unil.ch.
Carlotta GuiducciLaboratory of Life Sciences Electronics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland. Carlotta.guiducci@epfl.ch.
École Polytechnique Fédérale de Lausanne · CHUniversity of Lausanne · CHUniversity Hospital of Lausanne · CH

Funding

ETH Personalized Health and Related Technologies Initiative PHRT-308Innosuisse - Schweizerische Agentur für Innovationsförderung 56547.1Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 205321_179086Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung PP00P3_183725
6 · The paper itself

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

Indexed as

Bone MarrowHematopoietic Stem CellsAnimalsAntigens, CD34Bone Marrow CellsCell DifferentiationCell SeparationFlow CytometryHumansMegakaryocytesMiceMicrofluidicsAntigens, CD34

Identifiers

PMID38105340
PMCPMC10725893
OpenAlexW4389899927

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.