Phosphoproteomic profiling reveals a defined genetic program for osteoblastic lineage commitment of human bone marrow-derived stromal stem cells

Inigo Barrio-Hernandez, Abbas Jafari, Kristoffer T G Rigbolt, Philip Hallenborg, Virginia Sanchez-Quiles, Ida Skovrind, Vyacheslav Akimov, Irina Kratchmarova, Joern Dengjel, Moustapha Kassem, Blagoy Blagoev*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Bone marrow-derived mesenchymal stem cells (MSCs) differentiate into osteoblasts upon stimulation by signals present in their niche. Because the global signaling cascades involved in the early phases of MSCs osteoblast (OB) differentiation are not well-defined, we used quantitative mass spectrometry to delineate changes in human MSCs proteome and phosphoproteome during the first 24 h of their OB lineage commitment. The temporal profiles of 6252 proteins and 15,059 phosphorylation sites suggested at least two distinct signaling waves: one peaking within 30 to 60 min after stimulation and a second upsurge after 24 h. In addition to providing a comprehensive view of the proteome and phosphoproteome dynamics during early MSCs differentiation, our analyses identified a key role of serine/threonine protein kinase D1 (PRKD1) in OB commitment. At the onset of OB differentiation, PRKD1 initiates activation of the pro-osteogenic transcription factor RUNX2 by triggering phosphorylation and nuclear exclusion of the histone deacetylase HDAC7.

Original languageEnglish
JournalGenome Research
Volume30
Issue number1
Pages (from-to)127-137
Number of pages11
ISSN1088-9051
DOIs
Publication statusPublished - Jan 2020

Bibliographical note

© 2020 Barrio-Hernandez et al.; Published by Cold Spring Harbor Laboratory Press.

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