Evidence map›Paper›PMID 36934242›Full record

ArticleMolecular brain2023

Spatiotemporal expression patterns of genes coding for plasmalemmal chloride transporters and channels in neurological diseases.

Yanruo Huang, Qihang Wang, Yunsong Peng, Wenjie Du, Qi Wang, Jiangtao Qi, Zijian Hao, Yingwei Wang

Open access · goldFull text read
In one paragraph

Article in Molecular brain, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Gene Expression-Based Lesion-Symptom Mapping:The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Yanruo Huang *Department of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Qihang Wang *State Key Laboratory of Molecular Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, 200031, China.
Yunsong PengDivision of Life Sciences and Medicine, School of Biomedical Engineering (Suzhou), University of Science and Technology of China, Hefei, 230026, China.
Wenjie DuDepartment of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Qi WangDepartment of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Jiangtao QiDepartment of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Zijian HaoInstitute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, 200433, China. haozijian2008@163.com.
Yingwei WangDepartment of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, 200040, China. wangyw@fudan.edu.cn.ORCID 0000-0003-1633-8834
Fudan University · CNChinese Academy of Sciences · CNUniversity of Science and Technology of China · CN

Funding

Foundation of Shanghai Municipal Key Clinical Specialty shslczdzk06901National Natural Science Foundation of China 32200777National Natural Science Foundation of China 81730031National Natural Science Foundation of China 82001455
6 · The paper itself

Abstract

Neuronal voltage changes which are dependent on chloride transporters and channels are involved in forming neural functions during early development and maintaining their stability until adulthood. The intracellular chloride concentration maintains a steady state, which is delicately regulated by various genes coding for chloride transporters and channels (GClTC) on the plasmalemma; however, the synergistic effect of these genes in central nervous system disorders remains unclear. In this study, we first defined 10 gene clusters with similar temporal expression patterns, and identified 41 GClTC related to brain developmental process. Then, we found 4 clusters containing 22 GClTC were enriched for the neuronal functions. The GClTC from different clusters presented distinct cell type preferences and anatomical heterogeneity. We also observed strong correlations between clustered genes and diseases, most of which were nervous system disorders. Finally, we found that one of the most well-known GClTC, SLC12A2, had a more profound effect on glial cell-related diseases than on neuron-related diseases, which was in accordance with our observation that SLC12A2 was mainly expressed in oligodendrocytes during brain development. Our findings provide a more comprehensive understanding of the temporal and spatial expression characteristics of GClTC, which can help us understand the complex roles of GClTC in the development of the healthy human brain and the etiology of brain disorders.

Indexed as

Brain DiseasesChloridesBrainChloride ChannelsHumansMembrane Transport ProteinsNeurogliaSolute Carrier Family 12, Member 2Chloride ChannelsChloridesMembrane Transport ProteinsSLC12A2 protein, humanSolute Carrier Family 12, Member 2Chloride channelChloride transporterGene expression patternNeurodevelopmentSLC12A2

Identifiers

PMID36934242
PMCPMC10024392
OpenAlexW4327723546

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read3
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.