Evidence map›Paper›PMID 33037315›Full record

ArticleCommunications biology2020

Upconversion optogenetic micro-nanosystem optically controls the secretion of light-responsive bacteria for systemic immunity regulation.

Chun Yang, Meihui Cui, Yingying Zhang, Huizhuo Pan, Jing Liu, Shixing Wang, Ning Ma, Jin Chang, Tao Sun, Hanjie Wang

Erratum issuedAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Chun Yang *School of Life Sciences, Tianjin University, Tianjin, 300072, China.
Meihui Cui *School of Life Sciences, Tianjin University, Tianjin, 300072, China.
Yingying Zhang *School of Life Sciences, Tianjin University, Tianjin, 300072, China.
Huizhuo PanSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Jing LiuSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Shixing WangAcademy of Medical engineered and Translational Medicine, Tianjin University, Tianjin, 300072, China.
Ning MaSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Jin ChangSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Tao SunCenter for Biosafety Research and Strategy, Tianjin University, Tianjin, 300072, China. tsun@tju.edu.cn.ORCID http://orcid.org/0000-0002-7575-3483
Hanjie WangSchool of Life Sciences, Tianjin University, Tianjin, 300072, China. wanghj@tju.edu.cn.ORCID http://orcid.org/0000-0001-9400-814X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical molecules specifically secreted into the blood and targeted tissues by intestinal microbiota can effectively affect the associated functions of the intestine especially immunity, representing a new strategy for immune-related diseases. However, proper ways of regulating the secretion metabolism of specific strains still remain to be established. In this article, an upconversion optogenetic micro-nanosystem was constructed to effectively regulate the specific secretion of engineered bacteria. The system included two major modules: (i) Modification of secretory light-responsive engineered bacteria. (ii) Optical sensing mediated by upconversion optogenetic micro-nanosystem. This system could regulate the efficient secretion of immune factors by engineered bacteria through optical manipulation. Inflammatory bowel disease and subcutaneously transplanted tumors were selected to verify the effectiveness of the system. Our results showed that the endogenous factor TGF-β1 could be controllably secreted to suppress the intestinal inflammatory response. Additionally, regulatory secretion of IFN-γ was promoted to slow the progression of B16F10 tumor.

Indexed as

AnimalsBioengineeringCell Line, TumorColitis, UlcerativeEscherichia coliFemaleGastrointestinal MicrobiomeGene ExpressionHumansMaleMiceMice, Inbred C57BLNanotechnologyNeoplasm TransplantationOptogeneticsTransforming Growth Factor beta1Transforming Growth Factor beta1

Identifiers

PMID33037315
PMCPMC7547716

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.