Evidence map›Paper›PMID 18329265›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2008

Brain microglia express steroid-converting enzymes in the mouse.

Andres Gottfried-Blackmore, Amanda Sierra, Peter H Jellinck, Bruce S McEwen, Karen Bulloch

Open access · greenAbstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 86 citations in OpenAlex.

  1. The neuroimmune-glutamate hypothesis of addiction.Neuroscience and biobehavioral reviews · 2026
    Review
  2. Review
  3. Article
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  5. The Effects of Neuroactive Steroids on Myelin in Health and Disease.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2024
    Review
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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

5 authors at 2 institutions in 2 countries.

Andres Gottfried-BlackmoreLaboratory of Neuroendocrinology, Rockefeller University, 1230 York Avenue, New York, NY 10065, United States.
Amanda Sierra
Peter H Jellinck
Bruce S McEwen
Karen Bulloch
Rockefeller University · USQueen's University · CA

Funding

The Nonhuman Primate CoreP01AG016765 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MORRISON, JOHN H. · 1999 to 2016
$26.1M
NIA NIH HHS 5P01AG16765-07NIA NIH HHS P01 AG016765
6 · The paper itself

Abstract

In the CNS, steroid hormones play a major role in the maintenance of brain homeostasis and it's response to injury. Since activated microglia are the pivotal immune cell involved in neurodegeneration, we investigated the possibility that microglia provide a discrete source for the metabolism of active steroid hormones. Using RT-PCR, our results showed that mouse microglia expressed mRNA for 17beta-hydroxysteroid dehydrogenase type 1 and steroid 5alpha-reductase type 1, which are involved in the metabolism of androgens and estrogens. Microglia also expressed the peripheral benzodiazepine receptor and steroid acute regulatory protein; however, the enzymes required for de novo formation of progesterone and DHEA from cholesterol were not expressed. To test the function of these enzymes, primary microglia cultures were incubated with steroid precursors, DHEA and AD. Microglia preferentially produced delta-5 androgens (Adiol) from DHEA and 5alpha-reduced androgens from AD. Adiol behaved as an effective estrogen receptor agonist in neuronal cells. Activation of microglia with pro-inflammatory factors, LPS and INFgamma did not affect the enzymatic properties of these proteins. However, PBR ligands reduced TNFalpha production signifying an immunomodulatory role for PBR. Collectively, our results suggest that microglia utilize steroid-converting enzymes and related proteins to influence inflammation and neurodegeneration within microenvironments of the brain.

Indexed as

17-Hydroxysteroid Dehydrogenases3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrostenediolAnimalsBase SequenceBrainDNA PrimersGene ExpressionIn Vitro TechniquesLipopolysaccharidesMiceMice, Inbred C57BLMice, Inbred CBAMice, TransgenicMicrogliaReceptors, Estrogen17-Hydroxysteroid Dehydrogenases3 (or 17)-beta-hydroxysteroid dehydrogenase3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrostenediolBzrp protein, mouseDNA PrimersLipopolysaccharidesReceptors, EstrogenReceptors, GABARNA, MessengerSteroids

Identifiers

PMID18329265
PMCPMC2423427
OpenAlexW2036032721

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.