Tissue Preservation, Life care and Biobanking (B2B & Networking)

Circulating monocytes can transmigrate the vascular wall, enter a specifi c tissue, and diff erentiate into macrophages to perform functions relevant to that microenvironment (ME). Using the bone marrow as a model ME we focused on the ability of marrow fi broblasts to provide signals to monocytes. Th ese marrow fi broblasts appear to remain constant in their support of continuous “regeneration“, otherwise known as blood cell production. To study marrow fi broblasts we isolated and immortalized distinct fi broblast lines from normal human marrow: one designated HS27a expresses CD146, IGA3, and maintains early progenitors in culture. Monocytes co-cultured with HS27a assume a macrophage phenotype and express genes that function in tissue and organismal development. We also cloned a canine equivalent of HS27a, designated DS1, to be used in vivo in canine models of ischemia-induced myocardial infarction (MI) and radiation-induced pulmonary fi brosis (PF). 107 DS1 cells were infused intravenously aft er establishing the existence of an injury: 2 weeks post-infarction in the MI model and 5 weeks aft er irradiation in the PF model. In both, recovery of function was signifi cantly improved in dogs given DS1 cells compared to controls. Histological examination of tissue at necropsy also showed signifi cant diff erences between DS1 treated dogs and controls. Th e more complete tissue regeneration was observed in the lung model in which dogs were euthanized 21 weeks aft er treatment, whereas MI dogs were euthanized only 2 weeks aft er treatment. Importantly 48 hours aft er infusion there was no evidence by PCR of DS1 cells in the regenerating tissues or in the blood. Th is was in agreement with previous studies using 111In-DS1 cells which showed the DS1 cells are trapped in the lung where they are destroyed. However within 6 hours of DS1 infusion circulating monocytes expressed activation markers, and between 2 and7 days post DS1 infusion, large colonies of endothelial-like cells were grown from blood mononuclear cells. We propose that circulating monocytes come in contact with and receive signals from the DS1 cells sequestered in the lung. Th ese signals prepare the monocytes for recruitment to sites of injury where they scavenge debris and promote and regulate a multi-step process of endogenous regeneration.