Histological, immunohistochemical, and ultrastructural evaluation of mesenchymal stem cell-derived microvesicles versus granulocyte colony-stimulating factor in jejunal ischemia–reperfusion injury in albino rats

Intestinal ischemia-reperfusion injury (IIRI) is a life-threatening vascular emergency with high mortality, commonly occurring as a complication of hemorrhagic shock or acute mesenteric arterial occlusion. When revascularization is performed after this issue, injury will occur. The influence of MSC-MVs and G-CSF on IIRI was detected in this study. Fifty-six male adult albino rats were allocated into five groups: control, ischemia-reperfusion, MSC-MVs, G-CSF, and recovery. Ischemic injury was induced for one hour using micro-vascular clamp across the superior mesenteric artery at its beginning from the aorta. After that, the clamp was withdrawn to allow reperfusion for two hours. At the end of experimental period, rats were sacrificed. Jejunal tissues were processed for assessment of oxidative stress markers (MDA and SOD) as well as for histological and immune histo-chemical analysis. Ischemia-reperfusion group revealed highly statistically significant increase in tissue MDA while SOD showed the reverse, histologically by light microscopic examination; inflammatory cellular infiltration, congested blood vessels, and separated muscle fibers in muscularis mucosa were observed. Ultrastructurally, absorptive columnar cells appeared with heterochromatic nuclei, lost apical microvilli, and widen intercellular space. These findings showed more improvement in MSC-MVs group in comparison with G-CSF group while recovery group exhibited severe affection.

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Journal
Ultrastructural Pathology
Published
2026-03-23
DOI
https://doi.org/10.1080/01913123.2026.2643583
Primary Topic
Extracellular vesicles in disease
Type
article
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article

Histological, immunohistochemical, and ultrastructural evaluation of mesenchymal stem cell-derived microvesicles versus granulocyte colony-stimulating factor in jejunal ischemia–reperfusion injury in albino rats

Maha Mohammed, Hala M. Soliman, Alia Mahmoud, Heba M. Abdel-Aziz
Ultrastructural Pathology
Extracellular vesicles in disease
article

Histological, immunohistochemical, and ultrastructural evaluation of mesenchymal stem cell-derived microvesicles versus granulocyte colony-stimulating factor in jejunal ischemia–reperfusion injury in albino rats

Maha Mohammed, Hala M. Soliman, Alia Mahmoud, Heba M. Abdel-Aziz
article en

Abstract

Intestinal ischemia-reperfusion injury (IIRI) is a life-threatening vascular emergency with high mortality, commonly occurring as a complication of hemorrhagic shock or acute mesenteric arterial occlusion. When revascularization is performed after this issue, injury will occur. The influence of MSC-MVs and G-CSF on IIRI was detected in this study. Fifty-six male adult albino rats were allocated into five groups: control, ischemia-reperfusion, MSC-MVs, G-CSF, and recovery. Ischemic injury was induced for one hour using micro-vascular clamp across the superior mesenteric artery at its beginning from the aorta. After that, the clamp was withdrawn to allow reperfusion for two hours. At the end of experimental period, rats were sacrificed. Jejunal tissues were processed for assessment of oxidative stress markers (MDA and SOD) as well as for histological and immune histo-chemical analysis. Ischemia-reperfusion group revealed highly statistically significant increase in tissue MDA while SOD showed the reverse, histologically by light microscopic examination; inflammatory cellular infiltration, congested blood vessels, and separated muscle fibers in muscularis mucosa were observed. Ultrastructurally, absorptive columnar cells appeared with heterochromatic nuclei, lost apical microvilli, and widen intercellular space. These findings showed more improvement in MSC-MVs group in comparison with G-CSF group while recovery group exhibited severe affection.

Ultrastructural Pathology
Zagazig University (EG)
Good health and well-being
Openalex Percentile: Top 12%
Extracellular vesicles in disease
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