Evidence map›Paper›PMID 35533401›Full record

ArticleACS nano2022

Expansion Microscopy for Imaging the Cell-Material Interface.

Melissa L Nakamoto, Csaba Forró, Wei Zhang, Ching-Ting Tsai, Bianxiao Cui

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  13. Curved adhesions mediate cell attachment to soft matrix fibres in 3D.bioRxiv : the preprint server for biology · 2023
    Article
  14. Article
  15. Unique regulation of TiORegenerative biomaterials · 2023
    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

5 authors at 1 institution in 1 country.

Melissa L NakamotoDepartment of Chemistry, Stanford University, Stanford, California 94305, United States.ORCID 0000-0003-0955-6710
Csaba ForróDepartment of Chemistry, Stanford University, Stanford, California 94305, United States.
Wei ZhangDepartment of Chemistry, Stanford University, Stanford, California 94305, United States.
Ching-Ting TsaiDepartment of Chemistry, Stanford University, Stanford, California 94305, United States.
Bianxiao CuiDepartment of Chemistry, Stanford University, Stanford, California 94305, United States.ORCID 0000-0002-8044-5629
Stanford University · US

Funding

Nanoscale probes for sensing molecular functions in live cellsR35GM141598 · NIGMS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2021 to 2025
$3.4M
The role of membrane curvature in surface nanotopography-induced cell functionsR01GM128142 · NIGMS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2018 to 2020
$1.2M
NIGMS NIH HHS R01 GM128142NIGMS NIH HHS R35 GM141598
6 · The paper itself

Abstract

Surface topography on the scale of tens of nanometers to several micrometers substantially affects cell adhesion, migration, and differentiation. Recent studies using electron microscopy and super-resolution microscopy provide insight into how cells interact with surface nanotopography; however, the complex sample preparation and expensive imaging equipment required for these methods makes them not easily accessible. Expansion microscopy (ExM) is an affordable approach to image beyond the diffraction limit, but ExM cannot be readily applied to image the cell-material interface as most materials do not expand. Here, we develop a protocol that allows the use of ExM to resolve the cell-material interface with high resolution. We apply the technique to image the interface between U2OS cells and nanostructured substrates as well as the interface between primary osteoblasts with titanium dental implants. The high spatial resolution enabled by ExM reveals that although AP2 and F-actin both accumulate at curved membranes induced by vertical nanostructures, they are spatially segregated. Using ExM, we also reliably image how osteoblasts interact with roughened titanium implant surfaces below the diffraction limit; this is of great interest to understand osseointegration of the implants but has up to now been a significant technical challenge due to the irregular shape, the large volume, and the opacity of the titanium implants that have rendered them incompatible with other super-resolution techniques. We believe that our protocol will enable the use of ExM as a powerful tool for cell-material interface studies.

Indexed as

MicroscopyTitaniumOsseointegrationOsteoblastsSurface PropertiesTitaniumcell−material interfaceexpansion microscopyimplantmembrane curvaturenano-bio interfacenanotopography

Identifiers

PMID35533401
PMCPMC9879138
OpenAlexW4229440161

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.