Evidence map›Paper›PMID 36204248›Full record

ArticleResearch (Washington, D.C.)2022

High-Content Screening and Analysis of Stem Cell-Derived Neural Interfaces Using a Combinatorial Nanotechnology and Machine Learning Approach.

Letao Yang, Brian M Conley, Jinho Yoon, Christopher Rathnam, Thanapat Pongkulapa, Brandon Conklin, Yannan Hou, Ki-Bum Lee

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Boundarics in Biomedicine.Research (Washington, D.C.) · 2024
    Review
  9. 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

8 authors.

Letao YangDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.ORCID https://orcid.org/0000-0002-0572-9787
Brian M ConleyDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Jinho YoonDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Christopher RathnamDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Thanapat PongkulapaDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Brandon ConklinDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Yannan HouDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.
Ki-Bum LeeDepartment of Chemistry and Chemical Biology, Rutgers University, The State University of New Jersey, Piscataway, NJ 08854, USA.ORCID https://orcid.org/0000-0002-8164-0047

Funding

Translational Research in Regenerative MedicineT32EB005583 · NIBIB · RUTGERS, THE STATE UNIV OF N.J. · PI LEE, KIBUM, PAREKKADAN, BIJU · 2006 to 2022
$4.7M
Machine learning-enabled Comparative Transcriptomic Profiling to Validate NanoScript-induced Inner Ear Hair CellsR01DC016612 · NIDCD · RUTGERS, THE STATE UNIV OF N.J. · PI KWAN, KELVIN Y., LEE, KIBUM · 2018 to 2022
$2.8M
Training in Translating Neuroscience to TherapiesT32NS115700 · NINDS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI MOURADIAN, M. MARAL · 2021 to 2025
$1.4M
NIBIB NIH HHS T32 EB005583NIDCD NIH HHS R01 DC016612NINDS NIH HHS T32 NS115700
6 · The paper itself

Abstract

A systematic investigation of stem cell-derived neural interfaces can facilitate the discovery of the molecular mechanisms behind cell behavior in neurological disorders and accelerate the development of stem cell-based therapies. Nevertheless, high-throughput investigation of the cell-type-specific biophysical cues associated with stem cell-derived neural interfaces continues to be a significant obstacle to overcome. To this end, we developed a combinatorial nanoarray-based method for high-throughput investigation of neural interface micro-/nanostructures (physical cues comprising geometrical, topographical, and mechanical aspects) and the effects of these complex physical cues on stem cell fate decisions. Furthermore, by applying a machine learning (ML)-based analytical approach to a large number of stem cell-derived neural interfaces, we comprehensively mapped stem cell adhesion, differentiation, and proliferation, which allowed for the cell-type-specific design of biomaterials for neural interfacing, including both adult and human-induced pluripotent stem cells (hiPSCs) with varying genetic backgrounds. In short, we successfully demonstrated how an innovative combinatorial nanoarray and ML-based platform technology can aid with the rational design of stem cell-derived neural interfaces, potentially facilitating precision, and personalized tissue engineering applications.

Identifiers

PMID36204248
PMCPMC9513834

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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.