Evidence map›Paper›PMID 25359628›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2015

T cell-expressed CD40L potentiates the bone anabolic activity of intermittent PTH treatment.

Jerid W Robinson, Jau-Yi Li, Lindsey D Walker, Abdul Malik Tyagi, Michael A Reott, Mingcan Yu, Jonathan Adams, M Neale Weitzmann, Roberto Pacifici

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The role of WNT10B in physiology and disease: A 10-year update.Frontiers in cell and developmental biology · 2023
    Review
  4. Article
  5. Beyond Bone: Infectious Diseases and Immunity in Parathyroid Disorders.Advances in experimental medicine and biology · 2022
    Article
  6. Article
  7. Anabolic actions of PTH in murine models: two decades of insights.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  8. Role of Gut Microbiota in the Skeletal Response to PTH.The Journal of clinical endocrinology and metabolism · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The Cell Surface Markers Expression in Postmenopausal Women and Relation to Obesity and Bone Status.International journal of environmental research and public health · 2017
    Article
  17. Parathyroid Diseases and T Cells.Current osteoporosis reports · 2017
    Review
  18. Review
  19. Article
  20. Article
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

9 authors at 1 institution in 1 country.

Jerid W RobinsonDivision of Endocrinology, Metabolism and Lipids, Department of Medicine, Emory University, Atlanta, GA, USA.
Jau-Yi Li
Lindsey D Walker
Abdul Malik Tyagi
Michael A Reott
Mingcan Yu
Jonathan Adams
M Neale Weitzmann
Roberto Pacifici
Emory University · US

Funding

T CELLS AND PTH INDUCED BONE LOSSR01AR054625 · NIAMS · EMORY UNIVERSITY · PI PACIFICI, ROBERTO · 2007 to 2016
$3.3M
In Vivo MicroCT ScannerS10RR028009 · NCRR · EMORY UNIVERSITY · PI PACIFICI, ROBERTO · 2010 to 2010
$494k
The contribution of T cells to the anabolic activity of PTH in boneK01AR061453 · NIAMS · EMORY UNIVERSITY · PI LI, JAU-YI · 2012 to 2015
$382k
Immune Regulation of Bone HomeostasisI01BX000105 · VA · VETERANS HEALTH ADMINISTRATION · PI WEITZMANN, MERVYN NEALE · 2009 to 2022
–
BLRD VA I01 BX000105NCRR NIH HHS RR028009NCRR NIH HHS S10 RR028009NIAMS NIH HHS AR061453NIAMS NIH HHS AR54625NIAMS NIH HHS K01 AR061453NIAMS NIH HHS R01 AR054625
6 · The paper itself

Abstract

T cells are known to potentiate the bone anabolic activity of intermittent parathyroid hormone (iPTH) treatment. One of the involved mechanisms is increased T cell secretion of Wnt10b, a potent osteogenic Wnt ligand that activates Wnt signaling in stromal cells (SCs). However, additional mechanisms might play a role, including direct interactions between surface receptors expressed by T cells and SCs. Here we show that iPTH failed to promote SC proliferation and differentiation into osteoblasts (OBs) and activate Wnt signaling in SCs of mice with a global or T cell-specific deletion of the T cell costimulatory molecule CD40 ligand (CD40L). Attesting to the relevance of T cell-expressed CD40L, iPTH induced a blunted increase in bone formation and failed to increase trabecular bone volume in CD40L(-/-) mice and mice with a T cell-specific deletion of CD40L. CD40L null mice exhibited a blunted increase in T cell production of Wnt10b and abrogated CD40 signaling in SCs in response to iPTH treatment. Therefore, expression of the T cell surface receptor CD40L enables iPTH to exert its bone anabolic activity by activating CD40 signaling in SCs and maximally stimulating T cell production of Wnt10b.

Indexed as

Anabolic AgentsAnimalsBone and BonesCD40 LigandMiceMice, Inbred C57BLMice, KnockoutParathyroid HormoneT-LymphocytesAnabolic AgentsCD40 LigandParathyroid HormoneBMBONE MARROWOBOSTEOBLASTPARATHYROID HORMONEPPRPTHPTH/PTHRP RECEPTORSCSTROMAL CELL

Identifiers

PMID25359628
PMCPMC4376617
OpenAlexW1584935640

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.