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Article in English | MEDLINE | ID: mdl-38642731

ABSTRACT

Current treatments for schizophrenia (SCZ) remain largely ineffective in one-third of patients. Recent studies using stem cell therapy show a close relationship between stem cell immunomodulatory function and neuroinflammation in SCZ. To better investigate the efficacy of stem cell therapy for SCZ, human umbilical cord blood mesenchymal stem cells (hUC-MSC) with powerful immunomodulatory effects were administered to rats via the tail vein (once a week for 5 consecutive weeks starting from the weaning period) using a maternal immune activation (MIA) rodent model. Open field, PPI, Western blotting, Q-PCR, and immunofluorescence were used to assess the biological effects of repeated tail vein injections of hUC-MSC in offspring rats following the MIA model of SCZ. The results indicated that offspring of MIA rats exhibited schizophrenia-like (SCZ-like) anxiety behavior, with observed microglial activation triggering neuroinflammation. Furthermore, levels of IBA1, HMGB1, and PSD95 were significantly up-regulated, while SYP was significantly down-regulated. It is suggested that hUCB-MSCs may act through HMGB1, Iba1, PSD95, and related pathway molecules to alleviate neuroinflammation and repair synaptic damage by regulating the activity state of microglia. Consequently, this could improve the abnormal behavior observed in MIA offspring rats.


Subject(s)
Anxiety , Disease Models, Animal , HMGB1 Protein , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells , Microglia , Rats, Sprague-Dawley , Schizophrenia , Animals , Rats , Schizophrenia/therapy , Schizophrenia/chemically induced , Mesenchymal Stem Cell Transplantation/methods , Humans , Female , Anxiety/therapy , HMGB1 Protein/metabolism , Pregnancy , Disks Large Homolog 4 Protein/metabolism , Calcium-Binding Proteins/metabolism , Microfilament Proteins/metabolism , Male , Fetal Blood/cytology , Neuroinflammatory Diseases , Synaptophysin/metabolism , Cord Blood Stem Cell Transplantation/methods , Prenatal Exposure Delayed Effects
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