(Q27317423)

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Mesenchymal stem cells exhibit firm adhesion, crawling, spreading and transmigration across aortic endothelial cells: effects of chemokines and shear

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Mesenchymal stem cells exhibit firm adhesion, crawling, spreading and transmigration across aortic endothelial cells: effects of chemokines and shear (English)

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mesenchymal stem cell

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author name string

Giselle Chamberlain

1

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Helen Smith

2

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G Ed Rainger

3

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Jim Middleton

4

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language of work or name

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publication date

2011

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6

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9

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e25663

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copyright license

Creative Commons Attribution 4.0 International

28 September 2011

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April 2022 Public Data File from Crossref

copyright status

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1 reference

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1 reference

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7 April 2017

Therapeutic targeting of chemokine interactions in atherosclerosis

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Recent developments and complexities in neutrophil transmigration

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Lymphocyte crawling and transendothelial migration require chemokine triggering of high-affinity LFA-1 integrin.

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1 reference

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Chemokines in atherosclerosis: an update

1 reference

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Cells on the run: shear-regulated integrin activation in leukocyte rolling and arrest on endothelial cells

1 reference

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Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing.

1 reference

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Mesenchymal stem cells use integrin beta1 not CXC chemokine receptor 4 for myocardial migration and engraftment

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Importance of force linkage in mechanochemistry of adhesion receptors.

1 reference

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1 reference

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Mesenchymal stem cells transmigrate over the endothelial barrier

1 reference

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Agonist-induced endocytosis of CC chemokine receptor 5 is clathrin dependent.

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Nonhematopoietic mesenchymal stem cells can be mobilized and differentiate into cardiomyocytes after myocardial infarction

1 reference

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Mesenchymal stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182247

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Persistent induction of the chemokine receptor CXCR4 by TGF-beta 1 on synovial T cells contributes to their accumulation within the rheumatoid synovium.

1 reference

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Dynamics of neutrophil rolling over stimulated endothelium in vitro

1 reference

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Myocardium-targeted transplantation of mesenchymal stem cells by diagnostic ultrasound-mediated microbubble destruction improves cardiac function in myocardial infarction of New Zealand rabbits

1 reference

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1 reference

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1 reference

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Mesenchymal stem cells are recruited into wounded skin and contribute to wound repair by transdifferentiation into multiple skin cell type

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Successful treatment of refractory tibial nonunion using calcium sulphate and bone marrow stromal cell implantation.

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Potential risks of bone marrow cell transplantation into infarcted hearts

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Bone marrow mesenchymal stem cells express a restricted set of functionally active chemokine receptors capable of promoting migration to pancreatic islets

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Towards in situ tissue repair: human mesenchymal stem cells express chemokine receptors CXCR1, CXCR2 and CCR2, and migrate upon stimulation with CXCL8 but not CCL2.

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Bone marrow mesenchymal stem cells inhibit the response of naive and memory antigen-specific T cells to their cognate peptide.

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Differential MMP and TIMP production by human marrow and peripheral blood CD34(+) cells in response to chemokines.

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Adult stem cells from bone marrow (MSCs) isolated from different strains of inbred mice vary in surface epitopes, rates of proliferation, and differentiation potential

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Molecular trafficking mechanisms of multipotent mesenchymal stem cells derived from human bone marrow and placenta

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Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium: feasibility, cell migration, and body distribution.

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Locomotion of monocytes on endothelium is a critical step during extravasation

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Human bone marrow stromal cells express a distinct set of biologically functional chemokine receptors

1 reference

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based on heuristic

inferred from PubMed ID database lookup

Mesenchymal stem cells display coordinated rolling and adhesion behavior on endothelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

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based on heuristic

inferred from PubMed ID database lookup

Mesenchymal stem cells increase self-renewal of small intestinal epithelium and accelerate structural recovery after radiation injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human mesenchymal stem cells constitutively express chemokines and chemokine receptors that can be upregulated by cytokines, IFN-beta, and Copaxone

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The in vitro migration capacity of human bone marrow mesenchymal stem cells: comparison of chemokine and growth factor chemotactic activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone marrow-derived mesenchymal stem cells decrease acute graft-versus-host disease after allogeneic hematopoietic stem cells transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

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based on heuristic

inferred from PubMed ID database lookup

Targeted migration of mesenchymal stem cells modified with CXCR4 gene to infarcted myocardium improves cardiac performance

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of key mechanisms in transmigration and invasion of mesenchymal stem cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kinetics of the different steps during neutrophil migration through cultured endothelial monolayers treated with tumour necrosis factor-alpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0025663

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2011PLoSO...625663C

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release_q2ave6a3aregji4ms6d3hjf6ei

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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PubMed publication ID

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