Evidence map›Paper›PMID 26670737›Full record

ArticleNano letters2016

Nanoscale Patterning of Extracellular Matrix Alters Endothelial Function under Shear Stress.

Karina H Nakayama, Vinay N Surya, Monica Gole, Travis W Walker, Weiguang Yang, Edwina S Lai, Maggie A Ostrowski, Gerald G Fuller, Alexander R Dunn, Ngan F Huang

Open access · greenAbstract read
In one paragraph

Article in Nano letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Vascular endothelial integration of multiple biophysical stimuli.Frontiers in cardiovascular medicine · 2026
    Article
  5. Angiogenesis: Biological Mechanisms and In Vitro Models.Annals of biomedical engineering · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Production of Nanofibrillar Patterned Collagen for Tissue Engineering.Journal of visualized experiments : JoVE · 2024
    Article
  11. Review
  12. Bioengineering Cell Therapy for Treatment of Peripheral Artery Disease.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Review
  13. Article
  14. Review
  15. Biomedical Applications of Collagen.Bioengineering (Basel, Switzerland) · 2023
    Article
  16. Article
  17. Mechanical regulation of the early stages of angiogenesis.Journal of the Royal Society, Interface · 2022
    Review
  18. Review
  19. Review
  20. 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

10 authors at 4 institutions in 1 country.

Karina H NakayamaStanford Cardiovascular Institute , Stanford, California 94305, United States.
Vinay N SuryaStanford Cardiovascular Institute , Stanford, California 94305, United States.
Monica GoleVeterans Affairs Palo Alto Health Care System , Palo Alto, California 94304, United States.
Travis W WalkerDepartment of Chemical Engineering, Oregon State University , Corvallis, Oregon 97331, United States.
Weiguang YangDepartment of Pediatrics, Stanford School of Medicine , Stanford, California 94305, United States.
Edwina S LaiDepartment of Chemical Engineering, Stanford University School of Engineering , Stanford, California 94305, United States.
Maggie A OstrowskiDepartment of Chemical Engineering, Stanford University School of Engineering , Stanford, California 94305, United States.
Gerald G FullerDepartment of Chemical Engineering, Stanford University School of Engineering , Stanford, California 94305, United States.
Alexander R DunnStanford Cardiovascular Institute , Stanford, California 94305, United States.
Ngan F HuangStanford Cardiovascular Institute , Stanford, California 94305, United States.
Stanford University · USStanford Medicine · USVA Palo Alto Health Care System · USOregon State University · US

Funding

T32 Training Program in Mechanisms and Innovation in Vascular DiseaseT32HL098049 · NHLBI · STANFORD UNIVERSITY · PI Nicholas James Leeper, Philip S Tsao · 2010 to 2026
$6.3M
Molecular mechanisms underlying flow sensing in lymphatic endothelial cellsR01HL128779 · NHLBI · STANFORD UNIVERSITY · PI DUNN, ALEXANDER R, FULLER, GERALD · 2015 to 2018
$1.5M
Matrix-mediated endothelial differentiation of induced pluripotent stem cellsR00HL098688 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI HUANG, NGAN F. · 2013 to 2016
$742k
Injectable Hydrogels to Improve the Efficacy of iPSC-derived TherapiesR21EB020235 · NIBIB · STANFORD UNIVERSITY · PI HEILSHORN, SARAH C, HUANG, NGAN F. · 2015 to 2016
$433k
Vascularized Cardiac Patch with Physiological Orientation for Myocardial RepairI01BX002310 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI HUANG, NGAN F. · 2015 to 2018
–
BLRD VA I01 BX002310NHLBI NIH HHS 1T32HL098049NHLBI NIH HHS R00 HL098688NHLBI NIH HHS R00HL098688NHLBI NIH HHS R01 HL128779NHLBI NIH HHS R01HL128779-01NHLBI NIH HHS T32 HL098049NIBIB NIH HHS EB020235-01NIBIB NIH HHS R21 EB020235
6 · The paper itself

Abstract

The role of nanotopographical extracellular matrix (ECM) cues in vascular endothelial cell (EC) organization and function is not well-understood, despite the composition of nano- to microscale fibrillar ECMs within blood vessels. Instead, the predominant modulator of EC organization and function is traditionally thought to be hemodynamic shear stress, in which uniform shear stress induces parallel-alignment of ECs with anti-inflammatory function, whereas disturbed flow induces a disorganized configuration with pro-inflammatory function. Since shear stress acts on ECs by applying a mechanical force concomitant with inducing spatial patterning of the cells, we sought to decouple the effects of shear stress using parallel-aligned nanofibrillar collagen films that induce parallel EC alignment prior to stimulation with disturbed flow resulting from spatial wall shear stress gradients. Using real time live-cell imaging, we tracked the alignment, migration trajectories, proliferation, and anti-inflammatory behavior of ECs when they were cultured on parallel-aligned or randomly oriented nanofibrillar films. Intriguingly, ECs cultured on aligned nanofibrillar films remained well-aligned and migrated predominantly along the direction of aligned nanofibrils, despite exposure to shear stress orthogonal to the direction of the aligned nanofibrils. Furthermore, in stark contrast to ECs cultured on randomly oriented films, ECs on aligned nanofibrillar films exposed to disturbed flow had significantly reduced inflammation and proliferation, while maintaining intact intercellular junctions. This work reveals fundamental insights into the importance of nanoscale ECM interactions in the maintenance of endothelial function. Importantly, it provides new insight into how ECs respond to opposing cues derived from nanotopography and mechanical shear force and has strong implications in the design of polymeric conduits and bioengineered tissues.

Indexed as

Cell TrackingStress, MechanicalBlood VesselsCell MovementCell ProliferationCollagenEndothelial CellsExtracellular MatrixHumansNanofibersTissue EngineeringCollagencollagenendothelial cellinflammationNanofibrillar scaffoldpatterning

Identifiers

PMID26670737
PMCPMC4758680
OpenAlexW2276606014

What Socratic 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 Socratic graph.