TY - JOUR
T1 - A Systematic Review of the Evidence of Hematopoietic Stem Cell Differentiation to Fibroblasts
AU - Smilde, B.J.
AU - Botman, E.
AU - de Vries, T.J.
AU - de Vries, R.
AU - Micha, D.
AU - Schoenmaker, T.
AU - Janssen, J.J.W.M.
AU - Eekhoff, E.M.W.
N1 - This article belongs to the Special Issue: Mechanisms and Therapeutic Potential of Mesenchymal Stem Cells (MSCs). Publisher copyright: © 2022 by the authors.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Fibroblasts have an important role in the maintenance of the extracellular matrix of connective tissues by producing and remodelling extracellular matrix proteins. They are indispensable for physiological processes, and as such also associate with many pathological conditions. In recent years, a number of studies have identified donor-derived fibroblasts in various tissues of bone marrow transplant recipients, while others could not replicate these findings. In this systematic review, we provide an overview of the current literature regarding the differentiation of hematopoietic stem cells into fibroblasts in various tissues. PubMed, Embase, and Web of Science (Core Collection) were systematically searched for original articles concerning fibroblast origin after hematopoietic stem cell transplantation in collaboration with a medical information specialist. Our search found 5421 studies, of which 151 were analysed for full-text analysis by two authors independently, resulting in the inclusion of 104 studies. Only studies in animals and humans, in which at least one marker was used for fibroblast identification, were included. The results were described per organ of fibroblast engraftment. We show that nearly all mouse and human organs show evidence of fibroblasts of hematopoietic stem cell transfer origin. Despite significant heterogeneity in the included studies, most demonstrate a significant presence of fibroblasts of hematopoietic lineage in non-hematopoietic tissues. This presence appears to increase after the occurrence of tissue damage.
AB - Fibroblasts have an important role in the maintenance of the extracellular matrix of connective tissues by producing and remodelling extracellular matrix proteins. They are indispensable for physiological processes, and as such also associate with many pathological conditions. In recent years, a number of studies have identified donor-derived fibroblasts in various tissues of bone marrow transplant recipients, while others could not replicate these findings. In this systematic review, we provide an overview of the current literature regarding the differentiation of hematopoietic stem cells into fibroblasts in various tissues. PubMed, Embase, and Web of Science (Core Collection) were systematically searched for original articles concerning fibroblast origin after hematopoietic stem cell transplantation in collaboration with a medical information specialist. Our search found 5421 studies, of which 151 were analysed for full-text analysis by two authors independently, resulting in the inclusion of 104 studies. Only studies in animals and humans, in which at least one marker was used for fibroblast identification, were included. The results were described per organ of fibroblast engraftment. We show that nearly all mouse and human organs show evidence of fibroblasts of hematopoietic stem cell transfer origin. Despite significant heterogeneity in the included studies, most demonstrate a significant presence of fibroblasts of hematopoietic lineage in non-hematopoietic tissues. This presence appears to increase after the occurrence of tissue damage.
KW - fibroblast
KW - fibrosis
KW - hematopoietic stem cell transplantation
KW - lineage
KW - mesenchymal stem cell
KW - origin
UR - http://www.scopus.com/inward/record.url?scp=85144834906&partnerID=8YFLogxK
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85144834906&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36551819
U2 - https://doi.org/10.3390/biomedicines10123063
DO - https://doi.org/10.3390/biomedicines10123063
M3 - Review article
C2 - 36551819
SN - 2227-9059
VL - 10
SP - 1
EP - 15
JO - Biomedicines
JF - Biomedicines
IS - 12
M1 - 3063
ER -