Evidence map›Paper›PMID 40449704›Full record

ArticleActa biomaterialia2025

Reciprocal folding dynamics in cellular networks at the stroma-basement membrane interface.

Youngmin Jo, Donghyun Yim, Chan E Park, Insung Yong, Jongbeom Lee, Kwang Ho Ahn, Chanhee Yang, Jae-Byum Chang, Taek-Soo Kim, Jennifer Hyunjong Shin and 2 more

Abstract read
In one paragraph

Article in Acta biomaterialia, 2025. 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

12 authors.

Youngmin JoDepartment of Bio and Brain Engineering, KAIST, Daejeon 34141, South Korea.
Donghyun YimWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
Chan E ParkDepartment of Materials Science and Engineering, KAIST, Daejeon 305-701, Korea.
Insung YongDepartment of Bio and Brain Engineering, KAIST, Daejeon 34141, South Korea.
Jongbeom LeeDepartment of Bio and Brain Engineering, KAIST, Daejeon 34141, South Korea.
Kwang Ho AhnDepartment of Mechanical Engineering, KAIST, Daejeon 305-701, Korea.
Chanhee YangDepartment of Mechanical Engineering, KAIST, Daejeon 305-701, Korea.
Jae-Byum ChangDepartment of Materials Science and Engineering, KAIST, Daejeon 305-701, Korea.
Taek-Soo KimDepartment of Mechanical Engineering, KAIST, Daejeon 305-701, Korea.
Jennifer Hyunjong ShinDepartment of Mechanical Engineering, KAIST, Daejeon 305-701, Korea.
Taeyoon KimWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA; Faculty of Science and Technology, Keio University, Kohoku Ward, Yokohama, Japan. Electronic address: kimty@purdue.edu.
Pilnam KimDepartment of Bio and Brain Engineering, KAIST, Daejeon 34141, South Korea. Electronic address: pkim@kaist.ac.kr.

Funding

Universal Roles of Force Generation and Transmission in Biological SystemsR01GM126256 · NIGMS · PURDUE UNIVERSITY · PI KIM, TAEYOON · 2017 to 2021
$2.3M
NIGMS NIH HHS R01 GM126256
6 · The paper itself

Abstract

Epithelium layer stands on a membrane, called basement membrane (BM) which serves as a boundary with the underlying stroma. While most studies on morphogenesis have focused on the epithelium-BM complex, the role of the BM-stroma interface remains poorly understood. In this study, we demonstrate how forces originating from the stromal layer contribute to tissue morphogenesis. Folds focalization at the BM-stroma interface is driven by mechanical instability, which arises from the fluidity of the stroma and the polarized tractional forces acting on the rigid membrane of stromal cell condensates. Stromal cells move towards the folded region by topographic guidance, while the concentration of forces intensifies. Through this process, stromal cells and folds engage in recursive interactions, resulting in the formation of a cellular network. Our observation provides a rational mechanism for pattern formation in a multi-layered living tissue. STATEMENT OF SIGNIFICANCE: This study addresses a crucial gap in understanding how stromal cells interact with the basement membrane to lead tissue surface morphogenesis. By developing a collagen-based, nanometer-thick engineered basement membrane, we demonstrate that the stromal cells exert traction forces on the basement membrane to fold. The folding process guides stromal cell migration, which in turn induces further folding in a recursive manner. The direction of folding, invagination or evagination, is determined by the stiffness difference between the stroma and the basement membrane. This model offers better understanding about how the basement membrane interacts with stromal cells to make evaginated network structures on tissue surface.

Indexed as

Basement MembraneStromal CellsAnimalsCell MovementHumansFolding instabilityMorphogenesisMultilayerTissue model

Identifiers

PMID40449704
PMCPMC12243605

What OpenQuestion holds

Textmetadata
LicenceTDM
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.