Evidence map›Paper›PMID 29793503›Full record

ArticleJournal of translational medicine2018

Abnormalities of hair structure and skin histology derived from CRISPR/Cas9-based knockout of phospholipase C-delta 1 in mice.

Yu-Min Liu, Wei Liu, Jun-Shuang Jia, Bang-Zhu Chen, Heng-Wei Chen, Yu Liu, Ya-Nan Bie, Peng Gu, Yan Sun, Dong Xiao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Phospholipase C-Delta1 Deletion Impairs Dermal Papilla Cell Function by Disrupting the HIF-1/MAPK Signaling Pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

11 authors at 3 institutions in 1 country.

Yu-Min LiuInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Wei LiuInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Jun-Shuang JiaGuangdong Provincial Key Laboratory of Cancer Immunotherapy Research and Guangzhou Key Laboratory of Tumor Immunology Research, Cancer Research Institute, Southern Medical University, Guangzhou, 510515, China.
Bang-Zhu ChenInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Heng-Wei ChenInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Yu LiuInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Ya-Nan BieInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Peng GuInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China.
Yan SunZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China. suny69@mail.sysu.edu.cn.
Dong XiaoInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China. Xiao_d@hotmail.com.
Wei-Wang GuInstitute of Comparative Medicine & Laboratory Animal Center, Southern Medical University, Guangzhou, 510515, China. Guww100@163.com.
Southern Medical University · CNSongshan Lake Materials Laboratory · CNSun Yat-sen University · CN

Funding

International Science and Technology Cooperation Project 2011DFA33290National Natural Science Foundation of China 31271042National Natural Science Foundation of China 81172587National Natural Science Foundation of China 81672689National Natural Science Foundation of China 81702778National Natural Science Foundation of China (CN) 81372896Science and Technology Planning Project of Guangdong Province of China 2010A011200003Science and Technology Planning Project of Guangdong Province of China 2012B011000004Science and Technology Planning Project of Guangdong Province of China 2012B061700099Science and Technology Planning Project of Guangdong Province of China 2013B060300013Science and Technology Planning Project of Guangdong Province of China 2017A010105017Science and Technology Planning Project of Guangdong Province of China 2017A030303018Science and Technology Planning Project of Guangdong Province of China 2017A030303019
6 · The paper itself

Abstract

backgroundHairless mice have been widely applied in skin-related researches, while hairless pigs will be an ideal model for skin-related study and other biomedical researches because of the similarity of skin structure with humans. The previous study revealed that hairlessness phenotype in nude mice is caused by insufficient expression of phospholipase C-delta 1 (PLCD1), an essential molecule downstream of Foxn1, which encouraged us to generate PLCD1-deficient pigs. In this study, we plan to firstly produce PLCD1 knockout (KO) mice by CRISPR/Cas9 technology, which will lay a solid foundation for the generation of hairless PLCD1 KO pigs.

methodsGeneration of PLCD1 sgRNAs and Cas 9 mRNA was performed as described (Shao in Nat Protoc 9:2493-2512, 2014). PLCD1-modified mice (F0) were generated via co-microinjection of PLCD1-sgRNA and Cas9 mRNA into the cytoplasm of C57BL/6J zygotes. Homozygous PLCD1-deficient mice (F1) were obtained by intercrossing of F0 mice with the similar mutation.

resultsPLCD1-modified mice (F0) showed progressive hair loss after birth and the genotype of CRISPR/Cas9-induced mutations in exon 2 of PLCD1 locus, suggesting the sgRNA is effective to cause mutations that lead to hair growth defect. Homozygous PLCD1-deficient mice (F1) displayed baldness in abdomen and hair sparse in dorsa. Histological abnormalities of the reduced number of hair follicles, irregularly arranged and curved hair follicles, epidermal hyperplasia and disturbed differentiation of epidermis were observed in the PLCD1-deficient mice. Moreover, the expression level of PLCD1 was significantly decreased, while the expression levels of other genes (i.e., Krt1, Krt5, Krt13, loricrin and involucrin) involved in the differentiation of hair follicle were remarkerably increased in skin tissues of PLCD1-deficient mice.

conclusionsIn conclusion, we achieve PLCD1 KO mice by CRISPR/Cas9 technology, which provide a new animal model for hair development research, although homozygotes don't display completely hairless phenotype as expected.

Indexed as

AnimalsBase SequenceCRISPR-Associated Protein 9CRISPR-Cas SystemsGene Expression RegulationHairMice, Inbred C57BLMice, KnockoutPhospholipase C deltaRNA, Guide, CRISPR-Cas SystemsSkinCRISPR-Associated Protein 9Phospholipase C deltaRNA, Guide, CRISPR-Cas SystemsCRISPR/Cas9 technologyHairlessNude micePhospholipase C-delta 1 (PLCD1)Tibet minipigs

Identifiers

PMID29793503
PMCPMC5968471
OpenAlexW2803184232

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.