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Lhx2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth

Overview of attention for article published in Development (09501991), March 2016
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Article details
Title
Lhx2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth
Published in
Development (09501991), March 2016
DOI 10.1242/dev.130898
Pubmed ID
Authors
Abstract

The transcription factor nuclear factor-kappa B (NF-κB) plays an essential role in epidermal appendage induction and morphogenesis. In the epidermis of mice lacking NF-κB activity, initiation of primary hair follicle pre-placode formation is observed, but these primitive structures fail to proliferate and generate placodes. NF-κB signaling is known to modulate activity of WNT and SHH signaling at early stages of hair follicle development, but these roles do not fully account for the phenotypes observed when this pathway is blocked. To identify additional NF-κB target genes we developed a novel method to isolate and transcriptionally profile primary hair follicle placodes with active NF-κB signaling. In parallel, we compared gene expression at the same developmental stage in embryos with compromised NF-κB signaling, and wild type littermate controls. In addition to corroborating established NF-κB functions, these analyses uncovered novel NF-κB target genes with potential roles in priming hair follicle placodes for down-growth. Of particular interest, we identify the LIM/homeobox transcription factor LHX2 as a direct NF-κB target gene in this system, and show that loss of LHX2 replicates a subset of the phenotypes seen in embryos with reduced NF-κB signaling. LHX2 and TGFβ2 knockout embryos exhibit very similar abnormalities in hair follicle development, including failure of E-cadherin suppression that is required for follicle down-growth. Consistent with this, we find that TGFβ2 signaling is deficient in embryos with either inhibited NF-κB signaling or loss of LHX2. Furthermore, although TGFβ2 is not a direct LHX2 target gene, we find that exogenous TGFβ2 rescues the hair follicle phenotypes of LHX2 knockout skin explants, indicating that it operates downstream of LHX2. These findings identify a novel NF-κB-LHX2-TGFβ2 signaling axis that is critical for primary hair follicle morphogenesis and may function more broadly in development and disease.

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Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 44 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Unknown 44 100%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 9 20%
Student > Ph. D. Student 7 16%
Student > Master 5 11%
Student > Bachelor 4 9%
Student > Doctoral Student 2 5%
Other 2 5%
Unknown 15 34%
Readers by discipline
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 17 39%
Agricultural and Biological Sciences 5 11%
Medicine and Dentistry 3 7%
Immunology and Microbiology 2 5%
Arts and Humanities 1 2%
Other 2 5%
Unknown 14 32%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 13 May 2016.
All research outputs
#24,235,216
of 34,526,284 outputs
Outputs from Development (09501991)
#9,652
of 11,559 outputs
Outputs of similar age
#216,300
of 338,032 outputs
Outputs of similar age from Development (09501991)
#95
of 114 outputs
Altmetric has tracked 34,526,284 research outputs across all sources so far. This one is in the 28th percentile – i.e., 28% of other outputs scored the same or lower than it.
So far Altmetric has tracked 11,559 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.7. This one is in the 15th percentile – i.e., 15% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 338,032 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 33rd percentile – i.e., 33% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 114 others from the same source and published within six weeks on either side of this one. This one is in the 15th percentile – i.e., 15% of its contemporaries scored the same or lower than it.