Evidence map›Paper›PMID 27596508›Full record

ArticleMolecular neurobiology2017

Apical Polarization of SVCT2 in Apical Radial Glial Cells and Progenitors During Brain Development.

C Silva-Álvarez, K Salazar, P Cisternas, F Martínez, S Liour, N Jara, R Bertinat, F Nualart

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Role of vitamin C and SVCT2 in neurogenesis.Frontiers in neuroscience · 2023
    Review
  2. Article
  3. Article
  4. Review
  5. Two Distinct Faces of Vitamin C: AA vs. DHA.Antioxidants (Basel, Switzerland) · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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 2 institutions in 2 countries.

C Silva-ÁlvarezCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
K SalazarCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
P CisternasCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
F MartínezCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
S LiourFountain Biopharma Inc., Taipei, Taiwan.
N JaraCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
R BertinatCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile.
F NualartCenter for Advanced Microscopy CMA BIO-BIO, Concepcion University, Concepcion, Chile. frnualart@udec.cl.
University of Concepción · CLFountain Biopharma (Taiwan) · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During brain development, radial glial (RG) cells and the different progenitor subtypes are characterized by their bipolar morphology that includes an ovoid cell body and one or two radial processes that span across the developing cerebral wall. Different cells transport the reduced form of vitamin C, ascorbic acid (AA), using sodium-dependent ascorbic acid cotransporters (SVCT1 or SVCT2). SVCT2 is mainly expressed in the nervous system (CNS); however, its localization in the central nervous system during embryonic development along with the mechanism by which RG take up vitamin C and its intracellular effects is unknown. Thus, we sought to determine the expression and localization of SVCT2 during CNS development. SVCT2 is preferentially localized in the RG body at the ventricular edge of the cortex during the neurogenic stage (E12 to E17). The localization of SVCT2 overexpressed by in utero electroporation of E14 embryos is consistent with ventricular polarization. A similar distribution pattern was observed in human brain tissue sections at 9 weeks of gestation; however, SVCT2 immunoreaction was also detected in the inner and outer subventricular zone (SVZ). Finally, we used C17.2 neural stem cell line, J1ES cells and primary cell cultures derived from the brain cortex to analyze functional SVCT2 activity, AA effects in progenitor cells bipolar morphology, and SVCT2 expression levels in different culture conditions. Our results indicate that basal RG cells and apical intermediate and subapical progenitors are the main cell types expressing SVCT2 in the lissencephalic brain. SVCT2 was mainly detected in the apical region of the ventricular zone cells, contacting the cerebrospinal fluid. In gyrencephalic brains, SVCT2 was also detected in progenitor cells located in the inner and outer SVZ. Finally, we defined that AA has a strong radializing (bipolar morphology) effect in progenitor cells in culture and the differentiation condition modulates SVCT2 expression.

Indexed as

AnimalsCell DifferentiationCells, CulturedCerebral CortexEpendymoglial CellsFemaleImmunohistochemistryMiceMice, Inbred C57BLNeural Stem CellsNeurogenesisNeuronsRats, Sprague-DawleySodium-Coupled Vitamin C TransportersStem CellsSlc23a2 protein, mouseSodium-Coupled Vitamin C TransportersBrain developmentPolarizationRadial gliaSVCT2Tanycytes

Identifiers

PMID27596508
OpenAlexW2509131198

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.