Evidence map›Paper›PMID 36699636›Full record

ArticleJBMR plus2023

Visualizing Cathepsin K-Cre Expression at the Single-Cell Level with GFP Reporters.

Wenhuan Chai, Weiwei Hao, Jintao Liu, Zhenglin Han, Shiyu Chang, Liben Cheng, Mingxin Sun, Guofang Yan, Zemin Liu, Yin Liu and 4 more

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2023. 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
1.5field-weighted citation impact, top 18% 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, 17 citations in OpenAlex.

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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

14 authors at 1 institution in 1 country.

Wenhuan ChaiLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Weiwei HaoLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Jintao LiuLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Zhenglin HanLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Shiyu ChangLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Liben ChengLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Mingxin SunLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Guofang YanLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Zemin LiuLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Yin LiuLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Guodong ZhangLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Li XingLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Hongqian ChenLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.
Peng LiuLaboratory of Bone & Adipose Biology Shanxi Medical University Taiyuan China.ORCID https://orcid.org/0000-0001-5607-2482
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Cre/lox system is a fundamental tool for functional genomic studies, and a number of Cre lines have been generated to target genes of interest spatially and temporally in defined cells or tissues; this approach has greatly expanded our knowledge of gene functions. However, the limitations of this system have recently been recognized, and we must address the challenge of so-called nonspecific/off-target effects when a Cre line is utilized to investigate a gene of interest. For example, cathepsin K (Ctsk) has been used as a specific osteoclast marker, and Cre driven by its promoter is widely utilized for osteoclast investigations. However, Ctsk-Cre expression has recently been identified in other cell types, such as osteocytes, periosteal stem cells, and tenocytes. To better understand Ctsk-Cre expression and ensure appropriate use of this Cre line, we performed a comprehensive analysis of Ctsk-Cre expression at the single-cell level in major organs and tissues using two green fluorescent protein (GFP) reporters (ROSA nT-nG and ROSA tdT) and a tissue clearing technique in young and aging mice. The expression profile was further verified by immunofluorescence staining and droplet digital RT-PCR. The results demonstrate that Ctsk-Cre is expressed not only in osteoclasts but also at various levels in osteoblast lineage cells and other major organs/tissues, particularly in the brain, kidney, pancreas, and blood vessels. Furthermore, Ctsk-Cre expression increases markedly in the bone marrow, skeletal muscle, and intervertebral discs in aging mice. These data will be valuable for accurately interpreting data obtained from in vivo studies using Ctsk-Cre mice to avoid potentially misleading conclusions. © 2022 The Authors.

Indexed as

AGINGCATHEPSIN KCREGFPSOSTEOBLASTSOSTEOCLASTS

Identifiers

PMID36699636
PMCPMC9850439
OpenAlexW4309526597

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.