Evidence map›Paper›PMID 30833597›Full record

ArticleScientific reports2019

Deletion of Limk1 and Limk2 in mice does not alter cochlear development or auditory function.

Qiaojun Fang, Yuhua Zhang, Peng Da, Buwei Shao, Haolai Pan, Zuhong He, Cheng Cheng, Dan Li, Jiaqi Guo, Xiaohan Wu and 10 more

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  5. Novel m.4268T>C mutation in the mitochondrial tRNAWorld journal of clinical cases · 2022
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  11. Auditory Neuropathy as the Initial Phenotype for Patients WithFrontiers in cell and developmental biology · 2021
    Article
  12. Frontiers in cell and developmental biology · 2021
    Article
  13. A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With aFrontiers in cell and developmental biology · 2021
    Article
  14. Deletion ofFrontiers in cell and developmental biology · 2021
    Article
  15. Article
  16. Article
  17. 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

20 authors.

Qiaojun FangDepartment of Biomedical Engineering, Southern University of Science and Technology, 518000, Shenzhen, China.
Yuhua ZhangKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Peng DaDepartment of Otolaryngology-Head and Neck Surgery, Affiliated Hospital of Nantong University, 226001, Nantong, China.
Buwei ShaoKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Haolai PanDepartment of Otolaryngology, Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, 600 Yishan Road, 200233, Shanghai, China.
Zuhong HeKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Cheng ChengKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Dan LiKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Jiaqi GuoKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Xiaohan WuKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Ming GuanDepartment of Otolaryngology, Hangzhou First People's Hospital, 310006, Hangzhou, Zhejiang, China.
Menghui LiaoKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Yuan ZhangKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Suhua ShaDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, 29425, Charleston, South Carolina, USA.
Zikai ZhouKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China.
Jian WangDepartment of Otolaryngology, Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, 600 Yishan Road, 200233, Shanghai, China.ORCID 0000-0003-3633-6799
Tian WangDepartment of Otolaryngology-Head and Neck Surgery, The second Xiangya Hospital, Central South University, 410011, Changsha, Hunan Province, China.
Kaiming SuDepartment of Otolaryngology, Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, 600 Yishan Road, 200233, Shanghai, China. 021china@sina.com.
Renjie ChaiKey Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, 210096, Nanjing, China. renjiec@seu.edu.cn.
Fangyi ChenDepartment of Biomedical Engineering, Southern University of Science and Technology, 518000, Shenzhen, China. chenfy@sustc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited hearing loss is associated with gene mutations that result in sensory hair cell (HC) malfunction. HC structure is defined by the cytoskeleton, which is mainly composed of actin filaments and actin-binding partners. LIM motif-containing protein kinases (LIMKs) are the primary regulators of actin dynamics and consist of two members: LIMK1 and LIMK2. Actin arrangement is directly involved in the regulation of cytoskeletal structure and the maturation of synapses in the central nervous system, and LIMKs are involved in structural plasticity by controlling the activation of the actin depolymerization protein cofilin in the olfactory system and in the hippocampus. However, the expression pattern and the role of LIMKs in mouse cochlear development and synapse function also need to be further studied. We show here that the Limk genes are expressed in the mouse cochlea. We examined the morphology and the afferent synapse densities of HCs and measured the auditory function in Limk1 and Limk2 double knockout (DKO) mice. We found that the loss of Limk1 and Limk2 did not appear to affect the overall development of the cochlea, including the number of HCs and the structure of hair bundles. There were no significant differences in auditory thresholds between DKO mice and wild-type littermates. However, the expression of p-cofilin in the DKO mice was significantly decreased. Additionally, no significant differences were found in the number or distribution of ribbon synapses between the DKO and wild-type mice. In summary, our data suggest that the Limk genes play a different role in the development of the cochlea compared to their role in the central nervous system.

Indexed as

Actin Depolymerizing FactorsActinsAnimalsCochleaHair Cells, AuditoryHearingLim KinasesMiceMice, KnockoutSynapsesActin Depolymerizing FactorsActinsLimk1 protein, mouseLimk2 protein, mouseLim Kinases

Identifiers

PMID30833597
PMCPMC6399249

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