Evidence map›Paper›PMID 34378533›Full record

ArticleeLife2021

A bone-specific adipogenesis pathway in fat-free mice defines key origins and adaptations of bone marrow adipocytes with age and disease.

Xiao Zhang, Hero Robles, Kristann L Magee, Madelyn R Lorenz, Zhaohua Wang, Charles A Harris, Clarissa S Craft, Erica L Scheller

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 46 citations in OpenAlex.

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  12. Bone marrow adipocytes: key players in vascular niches, aging, and disease.Frontiers in cell and developmental biology · 2025
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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

8 authors at 1 institution in 1 country.

Xiao Zhang *Division of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.ORCID https://orcid.org/0000-0003-2427-0147
Hero Robles *Division of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.ORCID https://orcid.org/0000-0002-6439-1309
Kristann L MageeDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.
Madelyn R LorenzDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.
Zhaohua WangDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.
Charles A HarrisDivision of Endocrinology, Metabolism & Lipid Research, Department of Medicine, Washington University, Saint Louis, United States.
Clarissa S CraftDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.
Erica L SchellerDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, Saint Louis, United States.ORCID https://orcid.org/0000-0002-1551-3816
Washington University in St. Louis · US

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
NIAMS NIH HHS P30 AR074992NIDDK NIH HHS P30 DK020579
6 · The paper itself

Abstract

Bone marrow adipocytes accumulate with age and in diverse disease states. However, their origins and adaptations in these conditions remain unclear, impairing our understanding of their context-specific endocrine functions and relationship with surrounding tissues. In this study, by analyzing bone and adipose tissues in the lipodystrophic 'fat-free' mouse, we define a novel, secondary adipogenesis pathway that relies on the recruitment of adiponectin-negative stromal progenitors. This pathway is unique to the bone marrow and is activated with age and in states of metabolic stress in the fat-free mouse model, resulting in the expansion of bone marrow adipocytes specialized for lipid storage with compromised lipid mobilization and cytokine expression within regions traditionally devoted to hematopoiesis. This finding further distinguishes bone marrow from peripheral adipocytes and contributes to our understanding of bone marrow adipocyte origins, adaptations, and relationships with surrounding tissues with age and disease.

Indexed as

AdipocytesAdipogenesisAdipose TissueAge FactorsAnimalsBone and BonesBone MarrowBone Marrow CellsCell DifferentiationFemaleHematopoiesisMaleMiceMice, Inbred C57BLMice, TransgenicOsteoblastsadipogenesisadiponectinagingbone marrow adipocytecell biologymetabolismmouseprogenitor cells

Identifiers

PMID34378533
PMCPMC8412938
OpenAlexW3192883776

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.