Identification of Heparan-Sulfate Rich Cells in the Loose Connective Tissues of the Axolotl (Ambystoma mexicanum) with the Potential to Mediate Growth Factor Signaling during Regeneration.

axolotl heparan sulfate morphogens mouse positional information regeneration

Journal

Regenerative engineering and translational medicine
ISSN: 2364-4133
Titre abrégé: Regen Eng Transl Med
Pays: Switzerland
ID NLM: 101669762

Informations de publication

Date de publication:
Mar 2020
Historique:
entrez: 22 3 2021
pubmed: 23 3 2021
medline: 23 3 2021
Statut: ppublish

Résumé

Limb regeneration is the outcome of a complex sequence of events that are mediated by interactions between cells derived from the tissues of the amputated stump. Early in regeneration, these interactions are mediated by growth factor/morphogen signaling associated with nerves and the wound epithelium. One shared property of these proregenerative signaling molecules is that their activity is dependent on interactions with sulfated glycosaminoglycans (GAGs), heparan sulfate proteoglycan (HSPG) in particular, in the extracellular matrix (ECM). We hypothesized that there are cells in the axolotl that synthesize specific HSPGs that control growth factor signaling in time and space. In this study we have identified a subpopulation of cells within the ECM of axolotl skin that express high levels of sulfated GAGs on their cell surface. These cells are dispersed in a grid-like pattern throughout the dermis as well as the loose connective tissues that surround the tissues of the limb. These cells alter their morphology during regeneration, and are candidates for being a subpopulation of connective tissue cells that function as the cells required for pattern-formation during regeneration. Given their high level of HSPG expression, their stellate morphology, and their distribution throughout the loose connective tissues, we refer to these as the positional information GRID (Groups that are Regenerative, Interspersed and Dendritic) cells. In addition, we have identified cells that stain for high levels of expression of sulfated GAGs in mouse limb connective tissue that could have an equivalent function to GRID cells in the axolotl. The identification of GRID cells may have important implications for work in the area of Regenerative Engineering.

Identifiants

pubmed: 33748405
doi: 10.1007/s40883-019-00140-3
pmc: PMC7971174
mid: NIHMS1549212
doi:

Types de publication

Journal Article

Langues

eng

Pagination

7-17

Subventions

Organisme : NIAMS NIH HHS
ID : DP1 AR068147
Pays : United States
Organisme : NIAMS NIH HHS
ID : R33 AR073031
Pays : United States
Organisme : NIAMS NIH HHS
ID : R61 AR073031
Pays : United States

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Auteurs

T Otsuka (T)

Connecticut Convergence Institute for Translation in Regenerative Engineering, University of Connecticut Health, Farmington, CT 06030.
Raymond and Beverly Sackler Center for Biological, Physical and Engineering Sciences, University of Connecticut Health, CT 06030.
Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT 06030.

A Q Phan (AQ)

Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093.

C T Laurencin (CT)

Connecticut Convergence Institute for Translation in Regenerative Engineering, University of Connecticut Health, Farmington, CT 06030.
Raymond and Beverly Sackler Center for Biological, Physical and Engineering Sciences, University of Connecticut Health, CT 06030.
Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT 06030.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT 06269.
Department of Materials Science and Engineering, University of Connecticut, Storrs, CT 06269.
Department of Chemical and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269.

J D Esko (JD)

Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093.
Glycobiology Research and Training Center, University of California, San Diego, La Jolla, California 92093.

S V Bryant (SV)

Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697-2305.

D M Gardiner (DM)

Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697-2305.

Classifications MeSH