Evidence map›Paper›PMID 33003435›Full record

ArticleInternational journal of molecular sciences2020

High Mannose N-Glycans Promote Migration of Bone-Marrow-Derived Mesenchymal Stromal Cells.

Vivian Alonso-Garcia, Cutter Chaboya, Qiongyu Li, Bryan Le, Timothy J Congleton, Jose Florez, Victoria Tran, Gang-Yu Liu, Wei Yao, Carlito B Lebrilla and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Reducing Sialylation Enhances Electrotaxis of Corneal Epithelial Cells.International journal of molecular sciences · 2023
    Article
  5. Article
  6. Antitumor activity of a lectibody targeting cancer-associated high-mannose glycans.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  7. 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

11 authors at 2 institutions in 2 countries.

Vivian Alonso-GarciaStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.ORCID 0000-0002-2041-0053
Cutter ChaboyaStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.
Qiongyu LiDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0003-3654-0378
Bryan LeStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.
Timothy J CongletonStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.
Jose FlorezStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.
Victoria TranDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.
Gang-Yu LiuDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.
Wei YaoCenter for Musculoskeletal Health, Department of Internal Medicine, University of California Davis, Sacramento, CA 95817, USA.ORCID 0000-0002-1198-1161
Carlito B LebrillaDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.
Fernando A FierroStem Cell Program and Gene Therapy Center, University of California Davis, Sacramento, CA 95817, USA.ORCID 0000-0002-1086-2646
University of California, Davis · USUniversidade Federal de Uberlândia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For hundreds of indications, mesenchymal stromal cells (MSCs) have not achieved the expected therapeutic efficacy due to an inability of the cells to reach target tissues. We show that inducing high mannose N-glycans either chemically, using the mannosidase I inhibitor Kifunensine, or genetically, using an shRNA to silence the expression of mannosidase I A1 (MAN1A1), strongly increases the motility of MSCs. We show that treatment of MSCs with Kifunensine increases cell migration toward bone fracture sites after percutaneous injection, and toward lungs after intravenous injection. Mechanistically, high mannose N-glycans reduce the contact area of cells with its substrate. Silencing MAN1A1 also makes cells softer, suggesting that an increase of high mannose N-glycoforms may change the physical properties of the cell membrane. To determine if treatment with Kifunensine is feasible for future clinical studies, we used mass spectrometry to analyze the N-glycan profile of MSCs over time and demonstrate that the effect of Kifunensine is both transitory and at the expense of specific N-glycoforms, including fucosylations. Finally, we also investigated the effect of Kifunensine on cell proliferation, differentiation, and the secretion profile of MSCs. Our results support the notion of inducing high mannose N-glycans in MSCs in order to enhance their migration potential.

Indexed as

Antibodies, MonoclonalCell MovementGlycosylationHumansMannoseMannosidasesMesenchymal Stem CellsPolysaccharidesAntibodies, MonoclonalMannoseMannosidasesmannosyl-oligosaccharide 1,2-alpha-mannosidasePolysaccharidesamino-linked glycansbone fractureKifunensineMAN1A1mesenchymal stromal cellsmigration

Identifiers

PMID33003435
PMCPMC7582662
OpenAlexW3090008102

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.