Evidence map›Paper›PMID 31504222›Full record

ArticleBiology of reproduction2020

Enrichment of ovine gonadotropes via adenovirus gene targeting enhances assessment of transcriptional changes in response to estradiol-17 beta†.

Dilyara A Murtazina, Jesus Alejandro Arreguin-Arevalo, Jeremy D Cantlon, Ali Ebrahimpour-Boroojeny, Akash Shrestha, Jennifer A Hicks, Christianne Magee, Kelly Kirkley, Kenneth Jones, Terry M Nett and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biology of reproduction, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

12 authors at 2 institutions in 1 country.

Dilyara A MurtazinaDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Jesus Alejandro Arreguin-ArevaloDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Jeremy D CantlonDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Ali Ebrahimpour-BoroojenyDepartment of Computer Sciences, Colorado State University, Fort Collins, Colorado, USA.
Akash ShresthaDepartment of Computer Sciences, Colorado State University, Fort Collins, Colorado, USA.
Jennifer A HicksDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Christianne MageeDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Kelly KirkleyDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Kenneth JonesDepartment of Pediatrics, Section of Hematology, Oncology, and Bone Marrow Transplant, University of Colorado School of Medicine, Aurora, Colorado, USA.
Terry M NettDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Hamidreza ChitsazDepartment of Computer Sciences, Colorado State University, Fort Collins, Colorado, USA.
Colin M ClayDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Colorado State University · USUniversity of Colorado Denver · US

Funding

Physiological Mechanisms Underlying Heightened Responsiveness of Gonadotropes toR01HD065943 · NICHD · COLORADO STATE UNIVERSITY · PI CLAY, COLIN M · 2010 to 2014
$1.4M
Enrichment of a Gonadotrope Population for Cell Specific StudyR03HD085161 · NICHD · COLORADO STATE UNIVERSITY · PI CLAY, COLIN M · 2015 to 2016
$150k
NICHD NIH HHS R01 HD065943NICHD NIH HHS R03 HD085161
6 · The paper itself

Abstract

Gonadotropes represent approximately 5-15% of the total endocrine cell population in the mammalian anterior pituitary. Therefore, assessing the effects of experimental manipulation on virtually any parameter of gonadotrope biology is difficult to detect and parse from background noise. In non-rodent species, applying techniques such as high-throughput ribonucleic acid (RNA) sequencing is problematic due to difficulty in isolating and analyzing individual endocrine cell populations. Herein, we exploited cell-specific properties inherent to the proximal promoter of the human glycoprotein hormone alpha subunit gene (CGA) to genetically target the expression of a fluorescent reporter (green fluorescent protein [GFP]) selectively to ovine gonadotropes. Dissociated ovine pituitary cells were cultured and infected with an adenoviral reporter vector (Ad-hαCGA-eGFP). We established efficient gene targeting by successfully enriching dispersed GFP-positive cells with flow cytometry. Confirming enrichment of gonadotropes specifically, we detected elevated levels of luteinizing hormone (LH) but not thyrotropin-stimulating hormone (TSH) in GFP-positive cell populations compared to GFP-negative populations. Subsequently, we used next-generation sequencing to obtain the transcriptional profile of GFP-positive ovine gonadotropes in the presence or absence of estradiol 17-beta (E2), a key modulator of gonadotrope function. Compared to non-sorted cells, enriched GFP-positive cells revealed a distinct transcriptional profile consistent with established patterns of gonadotrope gene expression. Importantly, we also detected nearly 200 E2-responsive genes in enriched gonadotropes, which were not apparent in parallel experiments on non-enriched cell populations. From these data, we conclude that CGA-targeted adenoviral gene transfer is an effective means for selectively labeling and enriching ovine gonadotropes suitable for investigation by numerous experimental approaches.

Indexed as

AdenoviridaeAnimalsEstradiolGonadotrophsLuteinizing HormonePituitary Gland, AnteriorSheepThyrotropinEstradiolLuteinizing HormoneThyrotropinanterior pituitarygonadotropin-releasing hormone (GnRH/GnRH receptor): ovine/sheeptranscription

Identifiers

PMID31504222
PMCPMC7443347
OpenAlexW2969659797

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.