Evidence map›Paper›PMID 37761029›Full record

ArticleBiomedicines2023

Characterization of Distinct Chondrogenic Cell Populations of Patients Suffering from Microtia Using Single-Cell Micro-Raman Spectroscopy.

Dominika Zielinska, Hesham K Yosef, Tilo Zollitsch, Johann Kern, Yvonne Jakob, David Gvaramia, Nicole Rotter, Luca Pontiggia, Ueli Moehrlen, Thomas Biedermann and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 2 countries.

Dominika ZielinskaTissue Biology Research Unit, University Children's Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0001-7937-5216
Hesham K YosefFaculty of Medicine, University of Zurich, 8032 Zurich, Switzerland.ORCID 0000-0002-2385-0046
Tilo ZollitschmicrophotonXGmbH, 82327 Tutzing, Germany.
Johann KernDepartment of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.
Yvonne JakobDepartment of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.ORCID 0000-0001-7255-0333
David GvaramiaDepartment of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.ORCID 0000-0002-6013-3513
Nicole RotterDepartment of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.
Luca PontiggiaTissue Biology Research Unit, University Children's Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0002-5553-8997
Ueli MoehrlenTissue Biology Research Unit, University Children's Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0001-6418-1136
Thomas BiedermannTissue Biology Research Unit, University Children's Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0002-6438-8791
Agnes S KlarTissue Biology Research Unit, University Children's Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0003-3521-8010
University of Zurich · CHHeidelberg University · DE

Funding

Swiss National Science Foundation 316030_205706Swiss National Science Foundation CRSII5_173868
6 · The paper itself

Abstract

Microtia is a congenital condition of abnormal development of the outer ear. Tissue engineering of the ear is an alternative treatment option for microtia patients. However, for this approach, the identification of high regenerative cartilage progenitor cells is of vital importance. Raman analysis provides a novel, non-invasive, label-free diagnostic tool to detect distinctive biochemical features of single cells or tissues. Using micro-Raman spectroscopy, we were able to distinguish and characterize the particular molecular fingerprints of differentiated chondrocytes and perichondrocytes and their respective progenitors isolated from healthy individuals and microtia patients. We found that microtia chondrocytes exhibited lower lipid concentrations in comparison to healthy cells, thus indicating the importance of fat storage. Moreover, we suggest that collagen is a useful biomarker for distinguishing between populations obtained from the cartilage and perichondrium because of the higher spectral contributions of collagen in the chondrocytes compared to perichondrocytes from healthy individuals and microtia patients. Our results represent a contribution to the identification of cell markers that may allow the selection of specific cell populations for cartilage tissue engineering. Moreover, the observed differences between microtia and healthy cells are essential for gaining better knowledge of the cause of microtia. It can be useful for designing novel treatment options based on further investigations of the discovered biochemical substrate alterations.

Indexed as

chondrocytesmicrotiaperichondrocytesRaman spectroscopy

Identifiers

PMID37761029
PMCPMC10526501
OpenAlexW4386966713

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.