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Detection of human disease conditions by single-cell morpho-rheological phenotyping of blood.
eLife 7:e29213 (2018)
Blood is arguably the most important bodily fluid and its analysis provides crucial health status information. A first routine measure to narrow down diagnosis in clinical practice is the differential blood count, determining the frequency of all major blood cells. What is lacking to advance initial blood diagnostics is an unbiased and quick functional assessment of blood that can narrow down the diagnosis and generate specific hypotheses. To address this need, we introduce the continuous, cell-by-cell morpho-rheological (MORE) analysis of diluted whole blood, without labeling, enrichment or separation, at rates of 1000 cells/sec. In a drop of blood we can identify all major blood cells and characterize their pathological changes in several disease conditions in vitro and in patient samples. This approach takes previous results of mechanical studies on specifically isolated blood cells to the level of application directly in blood and adds a functional dimension to conventional blood analysis.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Acute Lymphoblastic-leukemia; Plasmodium-falciparum; Mechanical-properties; Deformability; Cytometry; Stiffness; Culture; Microcirculation; Synchronization; Palmitoylation
Language
english
Publication Year
2018
HGF-reported in Year
2018
ISSN (print) / ISBN
2050-084X
e-ISSN
2050-084X
Journal
eLife
Quellenangaben
Volume: 7,
Article Number: e29213
Publisher
eLife Sciences Publications
Publishing Place
Cambridge
Reviewing status
Peer reviewed
Institute(s)
Institute of Pancreatic Islet Research (IPI)
POF-Topic(s)
90000 - German Center for Diabetes Research
Research field(s)
Helmholtz Diabetes Center
PSP Element(s)
G-502600-002
WOS ID
WOS:000423511300001
Scopus ID
85042112938
PubMed ID
29331015
Erfassungsdatum
2018-03-02