Evidence map›Paper›PMID 40069211›Full record

ArticleNature communications2025

Responsive DNA artificial cells for contact and behavior regulation of mammalian cells.

Miao Wang, Hexin Nan, Meixia Wang, Sihui Yang, Lin Liu, Hong-Hui Wang, Zhou Nie

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Phase Separation of Nucleic Acids: Mechanisms, Properties, and Applications.Angewandte Chemie (International ed. in English) · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. ATP-Powered Signaling Between Artificial and Living Cells.Angewandte Chemie (International ed. in English) · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Engineering Motile Coacervate Droplets via Nanomotor Stabilization.Journal of the American Chemical Society · 2025
    Article
  12. 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

7 authors.

Miao WangState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China.
Hexin NanState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China.
Meixia WangState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China.
Sihui YangState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China.
Lin LiuState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China.
Hong-Hui WangState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China. wanghonghui@hnu.edu.cn.ORCID http://orcid.org/0000-0002-4420-9733
Zhou NieState Key Laboratory of Chemo and Biosensing, Hunan University, Changsha, PR China. niezhou.hnu@gmail.com.ORCID http://orcid.org/0000-0001-9864-2965

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21725503National Natural Science Foundation of China (National Science Foundation of China) 22034002National Natural Science Foundation of China (National Science Foundation of China) 22177030National Natural Science Foundation of China (National Science Foundation of China) 92253304
6 · The paper itself

Abstract

Artificial cells have emerged as synthetic entities designed to mimic the functionalities of natural cells, but their interactive ability with mammalian cells remains challenging. Herein, we develop a generalizable and modular strategy to engineer DNA-empowered stimulable artificial cells designated to regulate mammalian cells (STARM) via synthetic contact-dependent communication. Constructed through temperature-controlled DNA self-assembly involving liquid-liquid phase separation (LLPS), STARMs feature organized all-DNA cytoplasm-mimic and membrane-mimic compartments. These compartments can integrate functional nucleic acid (FNA) modules and light-responsive gold nanorods (AuNRs) to establish a programmable sense-and-respond mechanism to specific stimuli, such as light or ions, orchestrating diverse biological functions, including tissue formation and cellular signaling. By combining two designer STARMs into a dual-channel system, we achieve orthogonally regulated cellular signaling in multicellular communities. Ultimately, the in vivo therapeutic efficacy of STARM in light-guided muscle regeneration in living animals demonstrates the promising potential of smart artificial cells in regenerative medicine.

Indexed as

Artificial CellsDNAAnimalsCell CommunicationGoldHumansLightMiceNanotubesRegenerationRegenerative MedicineSignal TransductionDNAGold

Identifiers

PMID40069211
PMCPMC11897219

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.