GFAP and desmin expression in lymphatic tissues leads to difficulties in distinguishing between glial and stromal cells.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
25 06 2021
Historique:
received: 25 09 2020
accepted: 07 06 2021
entrez: 26 6 2021
pubmed: 27 6 2021
medline: 6 11 2021
Statut: epublish

Résumé

Recently, we found many immune cells including antigen presenting cells neurally hard wired in the T-cell zone of most lymphoid organs like amongst others, lymph nodes in rats, mice and humans. Single immune cells were reached by single neurites and enclosed with a dense neural meshwork. As it is well known that axons are always accompanied by glial cells, we were able to identify Schwann cells in the hilum, medullary and capsule region, like expected. Unexpected was the result, that we found oligodendrocyte-like cells in these regions, myelinating more than one axon. Likewise important was the finding, that one of the standard glial markers used, a polyclonal GFAP antibody equally bound to desmin and therefore marked nearly all stromal cells in cortical, paracortical and medullary cord regions. More detailed analysis showed that these results also appeared in many other non-lymphoid organs. Therefore, polyclonal GFAP antibodies are only conditionally usable for immunohistochemical analysis in peripheral tissues outside the central nervous system. It remains to be elucidated, if the binding of the GFAP antibody to desmin has its reason in a special desmin variant that can give stromal cells glial character.

Identifiants

pubmed: 34172765
doi: 10.1038/s41598-021-92364-z
pii: 10.1038/s41598-021-92364-z
pmc: PMC8233388
doi:

Substances chimiques

Desmin 0
Glial Fibrillary Acidic Protein 0
glial fibrillary astrocytic protein, mouse 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

13322

Commentaires et corrections

Type : ErratumIn

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Auteurs

Hauke Simon Günther (HS)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany. hauke@ini-research.org.

Stephan Henne (S)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

Jasmin Oehlmann (J)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

Julia Urban (J)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

Desiree Pleizier (D)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

Niclas Renevier (N)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

Christian Lohr (C)

Division of Neurophysiology, University of Hamburg, Hamburg, Germany.

Clemens Wülfing (C)

Group for Interdisciplinary Neurobiology and Immunology, Biozentrum Grindel, University of Hamburg, Hamburg, Germany.

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Classifications MeSH