Platelets Purification Is a Crucial Step for Transcriptomic Analysis.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
13 Mar 2022
Historique:
received: 26 01 2022
revised: 02 03 2022
accepted: 08 03 2022
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 9 4 2022
Statut: epublish

Résumé

Platelets are small anucleate cells derived from the fragmentation of megakaryocytes and are involved in different biological processes especially hemostasis, thrombosis, and immune response. Despite their lack of nucleus, platelets contain a reservoir of megakaryocyte-derived RNAs and all the machinery useful for mRNA translation. Interestingly, platelet transcriptome was analyzed in health and diseases and led to the identification of disease-specific molecular signatures. Platelet contamination by leukocytes and erythrocytes during platelet purification is a major problem in transcriptomic analysis and the presence of few contaminants in platelet preparation could strongly alter transcriptome results. Since contaminant impacts on platelet transcriptome remains theoretical, we aimed to determine whether low leukocyte and erythrocyte contamination could cause great or only minor changes in platelet transcriptome. Using microarray technique, we compared the transcriptome of platelets from the same donor, purified by common centrifugation method or using magnetic microbeads to eliminate contaminating cells. We found that platelet transcriptome was greatly altered by contaminants, as the relative amount of 8274 transcripts was different between compared samples. We observed an increase of transcripts related to leukocytes and erythrocytes in platelet purified without microbeads, while platelet specific transcripts were falsely reduced. In conclusion, serious precautions should be taken during platelet purification process for transcriptomic analysis, in order to avoid platelets contamination and result alteration.

Identifiants

pubmed: 35328521
pii: ijms23063100
doi: 10.3390/ijms23063100
pmc: PMC8953733
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Mohamad Chebbo (M)

Centre Cardiovasculaire et Nutrition, Aix-Marseille Université, INSERM, INRAE, 13005 Marseille, France.

Said Assou (S)

Institute for Regenerative Medicine and Biotherapy, Université de Montpellier, INSERM, Centre Hospitalier Universitaire de Montpellier, 34000 Montpellier, France.

Veronique Pantesco (V)

Institute for Regenerative Medicine and Biotherapy, Université de Montpellier, INSERM, Centre Hospitalier Universitaire de Montpellier, 34000 Montpellier, France.

Catherine Duez (C)

Centre Cardiovasculaire et Nutrition, Aix-Marseille Université, INSERM, INRAE, 13005 Marseille, France.

Marie C Alessi (MC)

Centre Cardiovasculaire et Nutrition, Aix-Marseille Université, INSERM, INRAE, 13005 Marseille, France.
Assistance Publique des Hôpitaux de Marseille, Hôpital de la Timone, Laboratoire d'hématologie, 13005 Marseille, France.

Pascal Chanez (P)

Centre Cardiovasculaire et Nutrition, Aix-Marseille Université, INSERM, INRAE, 13005 Marseille, France.
Assistance Publique des Hôpitaux de Marseille, Hôpital NORD, Clinique des Bronches, Allergies et Sommeil, 13015 Marseille, France.

Delphine Gras (D)

Centre Cardiovasculaire et Nutrition, Aix-Marseille Université, INSERM, INRAE, 13005 Marseille, France.

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Classifications MeSH