Evidence map›Paper›PMID 10330423›Full record

ArticleThe Journal of clinical investigation1999

Estrogen's bone-protective effects may involve differential IL-1 receptor regulation in human osteoclast-like cells.

T Sunyer, J Lewis, P Collin-Osdoby, P Osdoby

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 142 citations in OpenAlex.

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  11. Prostate cancer and osteoporosis.Current osteoporosis reports · 2013
    Article
  12. Review
  13. Decreased survival and hepato-renal pathology in mice with C-terminally truncated GP73 (GOLPH2).International journal of clinical and experimental pathology · 2009
    Article
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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

4 authors at 1 institution in 1 country.

T SunyerDepartment of Biology, and Division of Bone and Mineral Research, Washington University, St. Louis, Missouri 63130, USA.
J Lewis
P Collin-Osdoby
P Osdoby
Washington University in St. Louis · US

Funding

CELLULAR BASIS OF CRANIOFACIAL BONE DISORDERSR01DE006891 · NIDCR · WASHINGTON UNIVERSITY · PI OSDOBY, PHILIP A · 1986 to 2002
$652k
CYTOKINE RECEPTORS IN OSTEOCLASTSR03DE011166 · NIDCR · WASHINGTON UNIVERSITY · PI SUNYER, TERESA · 1994 to 1995
–
NIAMS NIH HHS R01 AR-32087NIA NIH HHS R01 AG-1543NIDCR NIH HHS R01 DE006891NIDCR NIH HHS R03 DE-11166-02
6 · The paper itself

Abstract

Declining estrogen levels during the first postmenopausal decade lead to rapid bone loss and increased fracture risk that can be reversed by estrogen replacement therapy. The bone-protective effects of estrogen may involve suppression of inflammatory cytokines that promote osteoclastogenesis and bone resorption, such as IL-1, TNF-alpha, and IL-6. We investigated whether estrogen modulates IL-1 actions on human osteoclasts (OCs) and other bone cell types. Isolated human OCs and primary bone marrow-derived OC-like cells expressed both the signaling (IL-1RI) and decoy (IL-1RII) IL-1 receptors, whereas only IL-1RI was detected in osteoblasts. IL-1RII/IL-1RI mRNA ratios and release of soluble IL-1RII (sIL-1RII) were lower in OC-like cells derived from women in the late postmenopausal period compared with younger women, but were unrelated to male donor age, suggesting that estrogen might play a role in regulating IL-1 receptor levels in vivo. Estrogen directly reduced in vitro OC-like cell IL-1RI mRNA levels while increasing IL-1RII mRNA levels and sIL-1RII release. These estrogenic events were associated with inhibited IL-1-mediated cytokine (IL-8) mRNA induction and cell survival, i.e., increased apoptosis. In contrast, estrogen did not alter IL-1R levels or IL-1 responsiveness in primary human osteoblasts or bone marrow stromal cells. We conclude that one novel mechanism by which estrogen exerts bone-protective effects may include a selective modulation of IL-1R isoform levels in OC or OC-like cells, thereby reducing their IL-1 responsiveness and cell survival. Conversely, this restraint on IL-1 actions may be lost as estrogen levels decline in aging women, contributing to an enhanced OC-mediated postmenopausal bone loss.

Indexed as

AgedBase SequenceCells, CulturedDNA PrimersEstradiolEstrogen Replacement TherapyEstrogensFemaleHumansInterleukin-1MaleMiddle AgedOsteoclastsOsteoporosis, PostmenopausalReceptors, Interleukin-1Receptors, Interleukin-1 Type IDNA PrimersEstradiolEstrogensInterleukin-1Receptors, Interleukin-1Receptors, Interleukin-1 Type IReceptors, Interleukin-1 Type IIRNA, Messenger

Identifiers

PMID10330423
PMCPMC408450
OpenAlexW2107925338

What OpenQuestion holds

Textmetadata
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.