Aging, rather than Parkinson's disease, affects the responsiveness of PBMCs to the immunosuppression of bone marrow mesenchymal stem cells Article Swipe
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· 2018
· Open Access
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· DOI: https://doi.org/10.3892/mmr.2018.9670
Whether aging or Parkinson's disease (PD) affects the responses of peripheral blood mononuclear cells (PBMCs) to immunosuppression by bone marrow‑derived mesenchymal stem cell (BM‑MSCs) and which cytokines are more effective in inducing BM‑MSCs to be immunosuppressive remains to be elucidated. PBMCs were isolated from healthy young (age 26‑35), healthy middle‑aged (age 56‑60) and middle‑aged PD‑affected individuals. All the recruits were male. The mitogen‑stimulated PBMCs and proinflammatory cytokine‑pretreated BM‑MSCs were co‑cultured. The PBMC proliferation was measured using Cell Counting Kit‑8, while the cytokine secretion was assayed by cytometric bead array technology. The immunosuppressive ability of BM‑MSCs was confirmed in young healthy, middle‑aged healthy and middle‑aged PD‑affected individuals. Among the three groups, the PBMC proliferation and cytokine secretion of the young healthy group were suppressed more significantly compared with those of the middle‑aged healthy and middle‑aged PD‑affected group. No significant differences were identified in the PBMC proliferation and cytokine secretion between the patients with PD and the middle‑aged healthy subjects. Interferon (IFN)‑γ synergized with tumor necrosis factor (TNF)‑α, interleukin (IL)‑1α or IL‑1β was more effective than either one alone, and the combinations of IFN‑γ + IL‑1α and IFN‑γ + IL‑1β were more effective than IFN‑γ + TNF‑α in inducing BM‑MSCs to inhibit PBMC proliferation. The results of the present study suggested that aging, rather than PD, affects the response of PBMCs toward the suppression of BM‑MSC, at least in middle‑aged males. Patients with PD aged 56‑60 remain eligible for anti‑inflammatory BM‑MSC‑based therapy. Treatment of BM‑MSCs with IFN‑γ + IL‑1α or IFN‑γ + IL‑1β prior to transplantation may result in improved immunosuppressive effects.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3892/mmr.2018.9670
- http://www.spandidos-publications.com/10.3892/mmr.2018.9670/download
- OA Status
- hybrid
- Cited By
- 3
- References
- 36
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W2901112719
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W2901112719Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.3892/mmr.2018.9670Digital Object Identifier
- Title
-
Aging, rather than Parkinson's disease, affects the responsiveness of PBMCs to the immunosuppression of bone marrow mesenchymal stem cellsWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2018Year of publication
- Publication date
-
2018-11-19Full publication date if available
- Authors
-
Yunqian Guan, Chunsong Zhao, Haiqiang Zou, Xiaoming Yan, Lu‐Lu Luo, Jialin Wu, Xiaobo Li, Yanwen ZhangList of authors in order
- Landing page
-
https://doi.org/10.3892/mmr.2018.9670Publisher landing page
- PDF URL
-
https://www.spandidos-publications.com/10.3892/mmr.2018.9670/downloadDirect link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
hybridOpen access status per OpenAlex
- OA URL
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https://www.spandidos-publications.com/10.3892/mmr.2018.9670/downloadDirect OA link when available
- Concepts
-
Peripheral blood mononuclear cell, Mesenchymal stem cell, Cytokine, Immunology, Medicine, Bone marrow, Proinflammatory cytokine, Immunosuppression, Stem cell, Interleukin 10, Tumor necrosis factor alpha, Biology, Inflammation, Pathology, In vitro, Biochemistry, GeneticsTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
3Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 1, 2022: 1, 2020: 1Per-year citation counts (last 5 years)
- References (count)
-
36Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.middle‑aged | 49, 53, 100, 103, 130, 133, 155, 227 |
| abstract_inverted_index.proliferation | 72, 112, 144 |
| abstract_inverted_index.significantly | 124 |
| abstract_inverted_index.co‑cultured. | 69 |
| abstract_inverted_index.proliferation. | 201 |
| abstract_inverted_index.proinflammatory | 65 |
| abstract_inverted_index.transplantation | 253 |
| abstract_inverted_index.BM‑MSC‑based | 238 |
| abstract_inverted_index.marrow‑derived | 19 |
| abstract_inverted_index.immunosuppression | 16 |
| abstract_inverted_index.immunosuppressive | 35, 91, 258 |
| abstract_inverted_index.anti‑inflammatory | 237 |
| abstract_inverted_index.mitogen‑stimulated | 62 |
| abstract_inverted_index.cytokine‑pretreated | 66 |
| cited_by_percentile_year.max | 95 |
| cited_by_percentile_year.min | 89 |
| countries_distinct_count | 1 |
| institutions_distinct_count | 8 |
| sustainable_development_goals[0].id | https://metadata.un.org/sdg/3 |
| sustainable_development_goals[0].score | 0.7699999809265137 |
| sustainable_development_goals[0].display_name | Good health and well-being |
| citation_normalized_percentile.value | 0.54844663 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |