Plasma-Based Scaffold Containing Bone-Marrow Mononuclear Cells Promotes Wound Healing in a Mouse Model of Pressure Injury

Author:

Alvarez-Viejo Maria123,Romero-Rosal Luis4,Perez-Basterrechea Marcos12,García-Gala Jose M.12,Hernando-Rodriguez Pablo2,Marana-Gonzalez Jesus5,Rubiera-Valdes Miriam6,Vivanco-Allende Blanca6,Fernandez-Rodriguez Angeles12,Martinez-Revuelta Eva12,Perez-Lopez Silvia12ORCID

Affiliation:

1. Unit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain

2. Health Research Institute of the Principality of Asturias-Foundation for Biomedical Research and Innovation in Asturias, Oviedo, Spain

3. University of Oviedo, Oviedo, Spain

4. Department of Plastic and Reconstructive Surgery, Central University Hospital of Asturias, Oviedo, Spain

5. Nuclear Medicine Unit, Leon University Healthcare Complex, Leon, Spain

6. Pathological Anatomy Service, Central University Hospital of Asturias, Oviedo, Spain

Abstract

Pressure injuries, or pressure ulcers, are a common problem that may lead to infections and major complications, besides being a social and economic burden due to the costs of treatment and hospitalization. While surgery is sometimes necessary, this also has complications such as recurrence or wound dehiscence. Among the newer methods of pressure injury treatment, advanced therapies are an interesting option. This study examines the healing properties of bone marrow mononuclear cells (BM-MNCs) embedded in a plasma-based scaffold in a mouse model. Pressure ulcers were created on the backs of mice (2 per mouse) using magnets and assigned to a group of ulcers that were left untreated (Control, n = 15), treated with plasma scaffold (Plasma, n = 15), or treated with plasma scaffold containing BM-MNC (Plasma + BM-MNC, n = 15). Each group was examined at three time points (3, 7, and 14 days) after the onset of treatment. At each time point, animals were subjected to biometric assessment, bioluminescence imaging, and tomography. Once treatment had finished, skin biopsies were processed for histological and wound healing reverse transcription polymerase chain reaction (RT-PCR) array studies. While wound closure percentages were higher in the Plasma and Plasma + BM-MNC groups, differences were not significant, and thus descriptive data are provided. In all individuals, the presence of donor cells was revealed by immunohistochemistry on posttreatment onset Days 3, 7, and 14. In the Plasma + BM-MNC group, less inflammation was observed by positron emission tomography–computed tomography (PET/CT) imaging of the mice at 7 days, and a complete morphometabolic response was produced at 14 days, in accordance with histological results. A much more pronounced inflammatory process was observed in controls than in the other two groups, and this persisted until Day 14 after treatment onset. RT-PCR array gene expression patterns were also found to vary significantly, with the greatest difference noted between both treatments at 14 days when 11 genes were differentially expressed.

Funder

Instituto de Salud Carlos III (ISCIII) co-funded by the European Union

Publisher

SAGE Publications

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