Mesenchymal stromal cell secretome for traumatic brain injury: Focus on immunomodulatory action

被引:21
|
作者
Pischiutta, Francesca [1 ]
Caruso, Enrico [1 ,2 ]
Cavaleiro, Helena [1 ,3 ,4 ,5 ]
Salgado, Antonio J. [3 ,4 ]
Loane, David J. [6 ]
Zanier, Elisa R. [1 ]
机构
[1] Ist Ric Farmacol Mario Negri IRCCS, Dept Neurosci, Milan, Italy
[2] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Anesthesia & Crit Care, Neurosci Intens Care Unit, Milan, Italy
[3] Univ Minho, Sch Med, Life & Hlth Sci Res Inst ICVS, Campus Gualtar, Braga, Portugal
[4] ICVS 3Bs PT Govt Associate Lab, Braga, Guimaraes, Portugal
[5] Stemmatters, Biotechnol & Regenerat Med, Guimaraes, Portugal
[6] Trinity Coll Dublin, Sch Biochem & Immunol, Trinity Biomed Sci Inst, Dublin, Ireland
关键词
Traumatic brain injury; Mesenchymal stromal cells; Secretome; Immunomodulation; Ageing; STEM-CELLS; T-CELLS; MATRIX METALLOPROTEINASES; CONDITIONED MEDIUM; ADIPOSE; INHIBIT; ACTIVATION; RECOVERY; PROTECT; BLOOD;
D O I
10.1016/j.expneurol.2022.114199
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The severity and long-term consequences of brain damage in traumatic brain injured (TBI) patients urgently calls for better neuroprotective/neuroreparative strategies for this devastating disorder. Mesenchymal stromal cells (MSCs) hold great promise and have been shown to confer neuroprotection in experimental TBI, mainly through paracrine mechanisms via secreted bioactive factors (i.e. secretome), which indicates significant potential for a cell-free neuroprotective approach. The secretome is composed of cytokines, chemokines, growth factors, proteins, lipids, nucleic acids, metabolites, and extracellular vesicles; it may offer advantages over MSCs in terms of delivery, safety, and variability of therapeutic response for brain injury. Immunomodulation by molecular factors secreted by MSCs is considered to be a key mechanism involved in their multi-potential therapeutic effects. Regulated neuroinflammation is required for healthy remodeling of central nervous system during development and adulthood. Moreover, immune cells and their secreted factors can also contribute to tissue repair and neurological recovery following acute brain injury. However, a chronic and maladaptive neuroinflammatory response can exacerbate TBI and contribute to progressive neurodegeneration and long-term neurological impairments. Here, we review the evidence for MSC-derived secretome as a therapy for TBI. Our framework incorporates a detailed analysis of in vitro and in vivo studies investigating the effects of the secretome on clinically relevant neurological and histopathological outcomes. We also describe the activation of immune cells after TBI and the immunomodulatory properties exerted by mediators released in the secretome. We then describe how ageing modifies central and systemic immune responses to TBI and discuss challenges and opportunities of developing secretome based neuroprotective therapies for elderly TBI populations. Finally, strategies aimed at modulating the secretome in order to boost its efficacy for TBI will also be discussed.
引用
收藏
页数:14
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