Evidence map›Paper›PMID 39068363›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Zebrafish Thrombocyte Transcriptome Analysis and Functional Genomics.

Weam Fallatah, Jabila Mary, Pudur Jagadeeswaran

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Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Weam FallatahDepartment of Biological Sciences, University of North Texas, Denton, TX, USA.
Jabila MaryDepartment of Biological Sciences, University of North Texas, Denton, TX, USA.
Pudur JagadeeswaranDepartment of Biological Sciences, University of North Texas, Denton, TX, USA. jag@unt.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our laboratory is interested in investigating the maturation process of zebrafish thrombocytes, which are functional equivalents to human platelets. We have adopted the zebrafish model to gain insights into mammalian platelet production, or thrombopoiesis. Notably, zebrafish exhibit two distinct populations of thrombocytes in their circulating blood: young and mature thrombocytes. This observation is intriguing because maturation appears to occur in circulation, yet the precise mechanisms governing this maturation remain elusive. Our goal is to understand the mechanisms underlying thrombocyte maturation by conducting single-cell RNA sequencing (scRNA-Seq) on young and mature thrombocytes, analyzing these transcriptomes to identify genes specific to each thrombocyte population, and elucidating the role of these genes in the maturation process, by quantifying thrombocyte numbers after the piggyback knockdown of each of these genes. In this chapter, we present a comprehensive, step-by-step protocol detailing the multifaceted methodology involved in understanding thrombocyte maturation, which encompasses the collection of zebrafish blood, the separation of young and mature thrombocytes using flow cytometry, scRNA-Seq analysis of these distinct thrombocyte populations, identification of genes specific to young and mature thrombocytes, and subsequent validation through gene knockdown techniques.

Indexed as

Blood PlateletsGene Expression ProfilingSingle-Cell AnalysisTranscriptomeZebrafishAnimalsFlow CytometryGenomicsHumansSequence Analysis, RNAThrombopoiesisBioinformaticsGFP+ thrombocytesPANTHERPiggyback knockdownPrimer 3RFP+ thrombocytesSingle-cell RNA-SeqThrombocyteTranscriptome

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Registered trials

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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.