Evidence map›Paper›PMID 33483474›Full record

ArticleCell death & disease2021

Role and dynamics of vacuolar pH during cell-in-cell mediated death.

Yan Su, He Ren, Meng Tang, You Zheng, Bo Zhang, Chenxi Wang, Xinyu Hou, Zubiao Niu, Zhongyi Wang, Xiaoyan Gao and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  14. A Balance Between Autophagy and Other Cell Death Modalities in Cancer.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Review
  16. Review
  17. Article
  18. 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

15 authors at 4 institutions in 2 countries.

Yan Su *CAS Key Laboratory of Mechanical Behavior and Design of Materials, Department of Modern Mechanics, University of Science and Technology of China, Hefei, China.
He Ren *Laboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Meng TangLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
You ZhengLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Bo ZhangLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Chenxi WangLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Xinyu HouDepartment of Oncology, Beijing Shijitan Hospital of Capital Medical University, Beijing, China.
Zubiao NiuLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Zhongyi WangLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Xiaoyan GaoLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Lihua GaoLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Hong JiangCollege of Life Science and Bioengineering, School of Science, Beijing Jiaotong University, Beijing, China.
Zhaolie ChenLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
Tianzhi LuoCAS Key Laboratory of Mechanical Behavior and Design of Materials, Department of Modern Mechanics, University of Science and Technology of China, Hefei, China. tzluo@ustc.edu.ORCID 0000-0003-2637-9605
Qiang SunLaboratory of Cell Engineering, Institute of Biotechnology, Beijing, China. sunq@bmi.ac.cn.ORCID 0000-0002-5342-0637
Capital Medical University · CNUniversity of Science and Technology of China · CNBeijing Jiaotong University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nonautonomous cell death by entosis was mediated by the so-called cell-in-cell structures, which were believed to kill the internalized cells by a mechanism dependent on acidified lysosomes. However, the precise values and roles of pH critical for the death of the internalized cells remained undetermined yet. We creatively employed keima, a fluorescent protein that displays different excitation spectra in responding to pH changes, to monitor the pH dynamics of the entotic vacuoles during cell-in-cell mediated death. We found that different cells varied in their basal intracellular pH, and the pH was relatively stable for entotic vacuoles containing live cells, but sharply dropped to a narrow range along with the inner cell death. In contrast, the lipidation of entotic vacuoles by LC3 displayed previously underappreciated complex patterns associated with entotic and apoptotic death, respectively. The pH decline seemed to play distinct roles in the two types of inner cell deaths, where apoptosis is preceded with moderate pH decline while a profound pH decline is likely to be determinate for entotic death. Whereas the cancer cells seemed to be lesser tolerant to acidified environments than noncancerous cells, manipulating vacuolar pH could effectively control inner cell fates and switch the ways whereby inner cell die. Together, this study demonstrated for the first time the pH dynamics of entotic vacuoles that dictate the fates of internalized cells, providing a rationale for tuning cellular pH as a potential way to treat cell-in-cell associated diseases such as cancer.

Indexed as

ApoptosisCell DeathHumansHydrogen-Ion ConcentrationTransfectionVacuoles

Identifiers

PMID33483474
PMCPMC7822940
OpenAlexW3124428400

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Registered trials

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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.