Osteoporosis, bone & mineral

Single-cell RNA sequencing reveals that an imbalance in monocyte subsets rather than changes in gene expression patterns is a feature of postmenopausal osteoporosis

J Bone Miner ResPublished Mechanistic study

Authors' conclusion

The scRNA-seq findings suggest that an imbalance in monocyte subsets is a characteristic feature of PMOP.

Study context

Population
Postmenopausal women; CD14+ bone marrow monocytes analysed by single-cell RNA sequencing (scRNA-seq)
Participants
3 vs 3
Comparison
Women with postmenopausal osteoporosis (PMOP) vs postmenopausal women with normal BMD
  • PMOPn = 3
  • Normal BMDn = 3reference
Outcome
Monocyte subset proportions (7 clusters)
Methodological detailssingle-cell RNA sequencing, bulk transcriptome validation (GEO), flow cytometry validation
  • Single-cell RNA sequencing
  • Bulk transcriptome validation (GEO)
  • Flow cytometry validation

Main finding

As reported in the abstract

  • Proportion of cluster 1 significantly decreased in PMOP
  • Proportion of cluster 7 increased in PMOP
  • Cluster 7: upregulated inflammation, immunity and osteoclast differentiation pathways; cluster 1 the opposite
  • Cluster 1 the initial subset; cluster 7 one of the terminal subsets
  • CD16 marker of cluster 7; increased proportion of CD16+ monocytes in PMOP

Further findings

Validation in bulk transcriptome data (GEO)

Altered proportions of clusters 1 and 7 validated and of diagnostic significance

Additional scRNA-seq of bone marrow mononuclear cells (3 PMOP, 3 normal BMD)

Differential proportions of clusters 1 and 7 confirmed again

Original publication

Single-cell RNA sequencing reveals that an imbalance in monocyte subsets rather than changes in gene expression patterns is a feature of postmenopausal osteoporosis. J Bone Miner Res. Published 23 April 2024. doi:10.1093/jbmr/zjae065

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.