dc.contributor.author
Bucher, Christian H.
dc.contributor.author
Schlundt, Claudia
dc.contributor.author
Wulsten, Dag
dc.contributor.author
Sass, F. Andrea
dc.contributor.author
Wendler, Sebastian
dc.contributor.author
Ellinghaus, Agnes
dc.contributor.author
Thiele, Tobias
dc.contributor.author
Seemann, Ricarda
dc.contributor.author
Willie, Bettina M.
dc.contributor.author
Volk, Hans-Dieter
dc.contributor.author
Duda, Georg N.
dc.contributor.author
Schmidt-Bleek, Katharina
dc.date.accessioned
2019-06-06T08:42:03Z
dc.date.available
2019-06-06T08:42:03Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/24689
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-2449
dc.description.abstract
Bone formation as well as bone healing capacity is known to be impaired in the elderly. Although bone formation is outpaced by bone resorption in aged individuals, we hereby present a novel path that considerably impacts bone formation and architecture: Bone formation is substantially reduced in aged individual owing to the experience of the adaptive immunity. Thus, immune-aging in addition to chronological aging is a potential risk factor, with an experienced immune system being recognized as more pro-inflammatory. The role of the aging immune system on bone homeostasis and on the bone healing cascade has so far not been considered. Within this study mice at different age and immunological experience were analyzed toward bone properties. Healing was assessed by introducing an osteotomy, immune cells were adoptively transferred to disclose the difference in biological vs. chronological aging. In vitro studies were employed to test the interaction of immune cell products (cytokines) on cells of the musculoskeletal system. In metaphyseal bone, immune-aging affects bone homeostasis by impacting bone formation capacity and thereby influencing mass and microstructure of bone trabeculae leading to an overall reduced mechanical competence as found in bone torsional testing. Furthermore, bone formation is also impacted during bone regeneration in terms of a diminished healing capacity observed in young animals who have an experienced human immune system. We show the impact of an experienced immune system compared to a naive immune system, demonstrating the substantial differences in the healing capacity and bone homeostasis due to the immune composition. We further showed that in vivo mechanical stimulation changed the immune system phenotype in young mice toward a more naive composition. While this rescue was found to be significant in young individuals, aged mice only showed a trend toward the reconstitution of a more naive immune phenotype. Considering the immune system's experience level in an individual, will likely allow one to differentiate (stratify) and treat (immune-modulate) patients more effectively. This work illustrates the relevance of including immune diagnostics when discussing immunomodulatory therapeutic strategies for the progressively aging population of the industrial countries.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
osteoimmunology
en
dc.subject
regeneration
en
dc.subject
bone healing
en
dc.subject
adaptive immunity
en
dc.subject
immune experience
en
dc.subject
inflamm-aging
en
dc.subject
biological aging
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
797
dcterms.bibliographicCitation.doi
10.3389/fimmu.2019.00797
dcterms.bibliographicCitation.journaltitle
Frontiers in Immunology
dcterms.bibliographicCitation.originalpublishername
Frontiers Media S.A.
dcterms.bibliographicCitation.volume
10
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31031773
dcterms.isPartOf.issn
1664-3224