Evidence map›Paper›PMID 34382379›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Humanized Biomimetic Nanovesicles for Neuron Targeting.

Assaf Zinger, Caroline Cvetkovic, Manuela Sushnitha, Tomoyuki Naoi, Gherardo Baudo, Morgan Anderson, Arya Shetty, Nupur Basu, Jennifer Covello, Ennio Tasciotti and 4 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

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  18. Research update on cell membrane camouflaged nanoparticles for cancer therapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  19. Humanized Biomimetic Nanovesicles for Neuron Targeting.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    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

14 authors at 4 institutions in 3 countries.

Assaf ZingerCenter for Musculoskeletal Regeneration, Houston Methodist Research Institute, Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.ORCID 0000-0001-7894-486X
Caroline CvetkovicCenter for Neuroregeneration, Houston Methodist Research Institute, Department of Neurosurgery, Houston Methodist Hospital, Houston, TX, 77030, USA.ORCID 0000-0002-3035-7313
Manuela SushnithaCenter for Musculoskeletal Regeneration, Houston Methodist Research Institute, Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Tomoyuki NaoiCenter for Musculoskeletal Regeneration, Houston Methodist Research Institute, Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Gherardo BaudoCenter for Musculoskeletal Regeneration, Houston Methodist Research Institute, Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Morgan AndersonCenter for Neuroregeneration, Houston Methodist Research Institute, Department of Neurosurgery, Houston Methodist Hospital, Houston, TX, 77030, USA.
Arya ShettyDepartment of BioSciences, Rice University, Houston, TX, 77030, USA.
Nupur BasuCenter for Neuroregeneration, Houston Methodist Research Institute, Department of Neurosurgery, Houston Methodist Hospital, Houston, TX, 77030, USA.
Jennifer CovelloDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Ennio TasciottiIRCCS San Raffaele Hospital, Rome, 00163, Italy.ORCID 0000-0003-1187-3205
Moran AmitDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Tongxin XieDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Francesca TaraballiCenter for Musculoskeletal Regeneration, Houston Methodist Research Institute, Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Robert KrencikCenter for Neuroregeneration, Houston Methodist Research Institute, Department of Neurosurgery, Houston Methodist Hospital, Houston, TX, 77030, USA.ORCID 0000-0002-2968-3162
Houston Methodist · USThe University of Texas MD Anderson Cancer Center · USRice University · USVita-Salute San Raffaele University · IT

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
Defining the Role of Tumor-Neutral Crosstalk in head and Neck Cancer Progression and Treatment ResistanceR37CA242006 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMIT, MORAN · 2020 to 2025
$3.4M
MicroBRAINS: Bioengineered Human Neural Circuits for Aging ResearchR21AG064567 · NIA · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KRENCIK, ROBERT CONRAD · 2019 to 2020
$444k
Targeting the JAK/STAT3 Pathway in Triple-Negative Breast Cancer Using Biomimetic NanoparticlesF31CA232705 · NCI · RICE UNIVERSITY · PI SUSHNITHA, MANUELA · 2018 to 2020
$121k
Cancer Prevention and Research Institute of Texas RP200655Michael J. Fox Foundation for Parkinson's Research 17871Moon Shots Program 1R37CA242006Moon Shots Program P30CA016672NCI NIH HHS 1R37CA242006NCI NIH HHS F31 CA232705NCI NIH HHS P30 CA016672NCI NIH HHS R37 CA242006NIA NIH HHS R21 AG064567NIH HHS R21AG064567NIH Ruth L. Kirschstein Research Service F31CA232705TIRR Foundation 019-114
6 · The paper itself

Abstract

Nanovesicles (NVs) are emerging as innovative, theranostic tools for cargo delivery. Recently, surface engineering of NVs with membrane proteins from specific cell types has been shown to improve the biocompatibility of NVs and enable the integration of functional attributes. However, this type of biomimetic approach has not yet been explored using human neural cells for applications within the nervous system. Here, this paper optimizes and validates the scalable and reproducible production of two types of neuron-targeting NVs, each with a distinct lipid formulation backbone suited to potential therapeutic cargo, by integrating membrane proteins that are unbiasedly sourced from human pluripotent stem-cell-derived neurons. The results establish that both endogenous and genetically engineered cell-derived proteins effectively transfer to NVs without disruption of their physicochemical properties. NVs with neuron-derived membrane proteins exhibit enhanced neuronal association and uptake compared to bare NVs. Viability of 3D neural sphere cultures is not disrupted by treatment, which verifies the utility of organoid-based approaches as NV testing platforms. Finally, these results confirm cellular association and uptake of the biomimetic humanized NVs to neurons within rodent cranial nerves. In summary, the customizable NVs reported here enable next-generation functionalized theranostics aimed to promote neuroregeneration.

Indexed as

AnimalsBiomimetic MaterialsBiomimeticsCell CommunicationExtracellular VesiclesHumansMaleMiceMice, Inbred C57BLNanostructuresNeuronsPluripotent Stem Cellsbiomimicryhuman pluripotent stem cellsnanovesiclesneuronsorganoids

Identifiers

PMID34382379
PMCPMC8498895
OpenAlexW3189043796

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.