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DPP4-Truncated CXCL12 Alters CXCR4/ACKR3 Signaling, Osteogenic Cell Differentiation, Migration, and Senescence

  • Ahmed M. Elmansi(corresponding author)
    ,
  • Nada H. Eisa
    ,
  • Sudharsan Periyasamy-Thandavan
    ,
  • Galina Kondrikova
    ,
  • Dmitry Kondrikov
    ,
  • Maggie M. Calkins
*Corresponding author for this work
  • Medical University of South Carolina
    ,
  • University of Michigan, Ann Arbor
    ,
  • Department of Veterans Affairs
    ,
  • Mansoura University
    ,
  • Augusta University
    ,
  • Medical College of Wisconsin
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Bone marrow skeletal stem cells (SSCs) secrete many cytokines including stromal derived factor-1 or CXCL12, which influences cell proliferation, migration, and differentiation. All CXCL12 splice variants are rapidly truncated on their N-terminus by dipeptidyl peptidase 4 (DPP4). This includes the common variant CXCL12 alpha (1-68) releasing a much less studied metabolite CXCL12(3-68). Here, we found that CXCL12(3-68) significantly inhibited SSC osteogenic differentiation and RAW-264.7 cell osteoclastogenic differentiation and induced a senescent phenotype in SSCs. Importantly, pre-incubation of SSCs with CXCL12(3-68) significantly diminished their ability to migrate toward CXCL12(1-68) in transwell migration assays. Using a high-throughput G-protein-coupled receptor (GPCR) screen (GPCRome) and bioluminescent resonance energy transfer molecular interaction assays, we revealed that CXCL12(3-68) acts via the atypical cytokine receptor 3-mediated β-arrestin recruitment and as a competitive antagonist to CXCR4-mediated signaling. Finally, a reverse phase protein array assay revealed that DPP4-cleaved CXCL12 possesses a different downstream signaling profile from that of intact CXCL12 or controls. The data presented herein provides insights into regulation of CXCL12 signaling. Importantly, it demonstrates that DPP4 proteolysis of CXCL12 generates a metabolite with significantly different and previously overlooked bioactivity that helps explain discrepancies in the literature. This also contributes to an understanding of the molecular mechanisms of osteoporosis and bone fracture repair and could potentially significantly affect the interpretation of experimental outcomes with clinical consequences in other fields where CXCL12 is vital, including cancer biology, immunology, cardiovascular biology, neurobiology, and associated pathologies.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 22-39 (18 pages)

Journal (Volume, Issue Number)

ACS Pharmacology and Translational Science (Volume 6, Issue 1)

Publication milestones

  • Accepted/In press - 2022
  • Published - 01/13/2023

Publication status

Published - 01/13/2023

Publication IDs

  • Scopus: 85143982229

Publication metrics

Metrics

Fractional count
6
Fractional count
0.32
Fractional count
13
Fractional count
0.68
Fractional count
6
Fractional count
1
Scopus
citations

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Citation count
12
Captures
18

Funding Details

This publication is based upon work supported in part by the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Clinical Science Research and Development Program (VA Merit Award 1I01CX000930-01, W.D.H.), the National Institutes of Health (NIA-AG036675 MEM-L and W.D.H.; AG067510 W.D.H. and MEM-L; R37 AI058072 B.F.V.), MUSC (W.D.H.), and the MUSC College of Medicine Enhancement of Team Science award (J.B.B.). The contents of this publication do not represent the views of the Department of Veterans Affairs or the United States Government. Some of the plasmids used in this work were generously provided by Dr. Françoise Bachelerie at Université Paris-Sud 11 and Dr. Nikolaus Heveker at the University of Montreal. The reverse phase protein array (RPPA) was done at the MD Anderson RPPA Core facility Funded by NCI # CA16672. The PRESTO-Tango GPCR screen and receptor agonist functional data were generously provided by the National Institute of Mental Health’s Psychoactive Drug Screening Program, Contract # HHSN-271-2018-00023 C (NIMH PDSP). The NIMH Psychoactive Drug Screening Program is directed by Bryan L. Roth at the University of North Carolina at Chapel Hill and Project Officer Jamie Driscoll at NIMH, Bethesda MD, USA. This publication is based upon work supported in part by the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Clinical Science Research and Development Program (VA Merit Award 1I01CX000930-01, W.D.H.), the National Institutes of Health (NIA-AG036675 MEM-L and W.D.H.; AG067510 W.D.H. and MEM-L; R37 AI058072 B.F.V.), MUSC (W.D.H.), and the MUSC College of Medicine Enhancement of Team Science award (J.B.B.). The contents of this publication do not represent the views of the Department of Veterans Affairs or the United States Government. Some of the plasmids used in this work were generously provided by Dr. Françoise Bachelerie at Université Paris-Sud 11 and Dr. Nikolaus Heveker at the University of Montreal. The reverse phase protein array (RPPA) was done at the MD Anderson RPPA Core facility Funded by NCI # CA16672. The PRESTO-Tango GPCR screen and receptor agonist functional data were generously provided by the National Institute of Mental Health’s Psychoactive Drug Screening Program, Contract # HHSN-271-2018-00023 C (NIMH PDSP). The NIMH Psychoactive Drug Screening Program is directed by Bryan L. Roth at the University of North Carolina at Chapel Hill and Project Officer Jamie Driscoll at NIMH, Bethesda MD, USA.(75)
FundersFunding numbers
NIH
NIA-AG036675 MEM-L, R37 AI058072, AG067510
NIMH
HHSN-271-2018-00023 C
NCI
CA16672
VA
-
ORD
1I01CX000930-01
MUSC
-
HSR&D
-