Effects of fresh bone marrow mononuclear cell therapy in rat model of retinopathy of prematurity

Retinopathy of prematurity (ROP) is a vasoproliferative disease that alters retinal vascular patterns in preterm neonates with immature retinal vasculature. This study was conducted to investigate the effects of cell therapy by bone marrow mononuclear cells (BMMNC) on neurological and vascular damag...

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Veröffentlicht in:Regenerative therapy 2023-12, Vol.24, p.43-53
Hauptverfasser: Tanourlouee, Saman Behboodi, Nasirzadeh, Mohammadreza, Zolbin, Masoumeh Majidi, Azimzadeh, Ashkan, Babaei, Javad Fahanik, Bitaraf, Masoud, Kajbafzadeh, Abdol-Mohammad, Masoumi, Ahmad, Hassani, Shokoufeh, Mirnia, Kayvan
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Sprache:eng
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Zusammenfassung:Retinopathy of prematurity (ROP) is a vasoproliferative disease that alters retinal vascular patterns in preterm neonates with immature retinal vasculature. This study was conducted to investigate the effects of cell therapy by bone marrow mononuclear cells (BMMNC) on neurological and vascular damages in a rat model of ROP. Ten newborn Wistar rats were divided randomly into the control and the oxygen-induced retinopathy (OIR) groups. Animals in the OIR group were incubated in an oxygen chamber to induce retinopathy. One eye of animals in the OIR group received BMMNC suspension (treated eyes), and the contralateral eye received the same volume of saline injection. Then, all animals underwent funduscopy, angiography, electroretinography, histopathology and immunohistochemical assessments. Compared to the saline injection group, eyes treated with BMMNC had less vascular tortuosity while veins and arteries had relatively the same caliber, as revealed by fundus examinations. Eyes in the treatment group showed significantly elevated photopic and scotopic B waves amplitude. Neovascularization in the inner retinal layer and apoptosis of neural retina cells in the treatment group was significantly lower compared to untreated eyes. Also, BMMNC transplantation decreased glial cell activation and VEGF expression in ischemic retina. Our results indicate that intravitreal injection of BMMNC reduces neural and vascular damages and results in recovered retinal function in rat model of ROP. Ease of extraction without in vitro processing, besides the therapeutic effects of BMMNCs, make this source of cells as a new choice of therapy for ROP or other retinal ischemic diseases. •Current ROP treatments are limited by disadvantages like inducing new vascular abnormalities, or disease recurrence.•Cell therapy, using specific cell lines, in animal models of ROP has reduced neural and vascular damages.•Bone marrow-derived mononuclear cells (BMMNC) is a heterogeneous population of cells and growth factors.•Fresh BMMNC can reduce neural-vascular damages and recover retinal function.•Fresh BMMNC is a potential low-cost, feasible therapeutic option for ROP or other retinal ischemic diseases.
ISSN:2352-3204
2352-3204
DOI:10.1016/j.reth.2023.05.009