Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing

被引:65
作者
Bucher, Christian H. [1 ,2 ,3 ]
Schlundt, Claudia [1 ,2 ,3 ]
Wulsten, Dag [1 ,2 ]
Sass, F. Andrea [1 ,2 ,3 ]
Wendler, Sebastian [1 ,2 ,3 ]
Ellinghaus, Agnes [1 ,2 ]
Thiele, Tobias [1 ,2 ]
Seemann, Ricarda [1 ,2 ]
Willie, Bettina M. [4 ]
Volk, Hans-Dieter [3 ,5 ]
Duda, Georg N. [1 ,2 ,3 ,6 ]
Schmidt-Bleek, Katharina [1 ,2 ,3 ]
机构
[1] Charite Univ Med Berlin, Julius Wolff Inst, Berlin, Germany
[2] Charite Univ Med Berlin, Ctr Musculoskeletal Surg, Berlin, Germany
[3] Charite Univ Med Berlin, Berlin Brandenburg Ctr Regenerat Therapies, Berlin, Germany
[4] McGill Univ, Fac Med, Dept Pediat Surg, Shriners Hosp Children, Montreal, PQ, Canada
[5] Charite Univ Med Berlin, Inst Med Immunol, Berlin, Germany
[6] Berlin Inst Hlth Ctr Regenerat Therapies, Berlin, Germany
关键词
osteoimmunology; regeneration; bone healing; T cells; adaptive immunity; immune experience; inflamm-aging; biological aging; AGE-RELATED-CHANGES; CORTICAL BONE; T-CELLS; B-CELLS; SUPPORT OSTEOCLASTOGENESIS; INTERFERON-GAMMA; OSTEOIMMUNOLOGY; FEMALE; MODEL; REGENERATION;
D O I
10.3389/fimmu.2019.00797
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:19
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