Evidence map›Paper›PMID 41668434›Full record

ArticleAdvanced healthcare materials2026

Dynamic Modulation of the Microenvironment Promotes Functional Maturation of Engineered Tissues.

Eric Silberman, Hadas Oved, Itay Gil, Amgad Marzook, Ester Sapir Baruch, Yahel Shechter, Assaf Shapira, Tal Dvir

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Eric SilbermanThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Hadas OvedThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Itay GilThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Amgad MarzookThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Ester Sapir BaruchThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Yahel ShechterThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Assaf ShapiraThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Tal DvirThe Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0002-3153-9928

Funding

ERC Consolidator 101001242Israeli Science Foundation 972/21Israeli Science Foundation- The Breakthrough Research Grants 1418/24NSF-BSF 220733
6 · The paper itself

Abstract

While extremely complex interactions between cells and extracellular matrix regulate cellular microenvironments in vivo, the pared-down complexity present in engineered tissues is generally insufficient to recapitulate these dynamics in vitro. Here, a biocompatible small molecule that can diffuse into tissues as they mature to dynamically modulate the cellular microenvironment is utilized. This technology can be deployed in multiple doses to repeatedly and controllably adjust the tissue's microenvironment as it matures. It is observed that deploying precisely the same concentration of the small molecule, but at different stages of a tissue's maturation, led to markedly different outcomes. In particular, it is shown that endothelial cells matured in dynamically modulated microenvironments form thicker, more native-like blood vessels than is possible using traditional, non-dynamic culture. Likewise, engineered cardiac tissues generated stronger contractions and demonstrated a more mature electrophysiology when encapsulated in a soft, dynamically modulated hydrogel matrix that allowed for tissue maturation. Finally, the results of differentiating induced pluripotent stem cells to cardiomyocytes within dynamic matrices and show that coordinating the tissue's stiffness with the differentiating cells' developmental stage maximizes their end functionality is presented. The ability to dynamically control the tissue microenvironment during maturation, in a facile and safe manner, represents a significant step toward achieving a more accurate in vitro recapitulation of complex processes vital for tissue engineering.

Indexed as

Cellular MicroenvironmentTissue EngineeringAnimalsCell DifferentiationEndothelial CellsExtracellular MatrixHumansHydrogelsInduced Pluripotent Stem CellsMyocytes, CardiacHydrogelsbiofabricationbiomaterialstissue engineeringtissue maturation

Identifiers

PMID41668434
PMCPMC13175298

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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.