Bone marrow-derived progenitor cells contribute to remodeling of the postpartum uterus
Autor: | Hugh S. Taylor, Fang Lyu, Alice Y. Chen, Nafeesa Abuwala, Jacqueline Kisa, Harvey J. Kliman, Reshef Tal, Shafiq Shaikh |
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Rok vydání: | 2021 |
Předmět: |
Stromal cell
Green Fluorescent Proteins Uterus Bone Marrow Cells Biology Article Andrology Mice Bone Marrow medicine Macrophage Animals Humans Progenitor cell Bone Marrow Transplantation Regeneration (biology) Stem Cells Postpartum Period Endothelial Cells Cell Biology Mice Inbred C57BL medicine.anatomical_structure Molecular Medicine Female Bone marrow Stem cell Postpartum period Developmental Biology |
Zdroj: | Stem Cells |
ISSN: | 1549-4918 |
Popis: | Endometrial stem/progenitor cells play a role in postpartum uterine tissue regeneration but the underlying mechanisms are poorly understood. While circulating bone marrow (BM)-derived cells (BMDCs) contribute to nonhematopoietic endometrial cells, the contribution of BMDCs to postpartum uterus remodeling is unknown. We investigated the contribution of BMDCs to the postpartum uterus using 5-fluorouracil-based non-gonadotoxic BM transplant from GFP donors into wild-type C57BL/6J female mice. Flow cytometry showed an influx of GFP+ cells to the uterus immediately postpartum accounting for 28.7% of total uterine cells, followed by a rapid decrease to pre-pregnancy levels. The majority of uterine GFP+ cells were CD45+ leukocytes and the proportion of nonhematopoietic CD45-GFP+ cells peaked on postpartum day (PPD) 1 (17.5%). Immunofluorescence colocalization of GFP with CD45 pan-leukocyte and F4/80 macrophage markers corroborated these findings. GFP+ cells were found mostly in subepithelial stromal location. Importantly, GFP+ cytokeratin-positive epithelial cells were found within the luminal epithelium exclusively on PPD1, demonstrating direct contribution to postpartum re-epithelialization. A subset (3.2%) of GFP+ cells were CD31 + CD45- endothelial cells, and found integrated within blood vessel endothelium. Notably, BM-derived GFP+ cells demonstrated preferential proliferation (PCNA+) and apoptosis (TUNEL+) on PPD1 vs resident GFP- cells, suggesting an active role for BMDCs in rapid tissue turnover. Moreover, GFP+ cells gradually acquired cell senescence together with decreased proliferation throughout the postpartum. In conclusion, BM-derived progenitors were found to have a novel nonhematopoietic cellular contribution to postpartum uterus remodeling. This contribution may have an important functional role in physiological as well as pathological postpartum endometrial regeneration. © AlphaMed Press 2021 SIGNIFICANCE STATEMENT: The uterus undergoes significant tissue regeneration in the postpartum period following parturition where endometrial stem cells are thought to play an important role. Here we show that bone marrow-derived progenitor cells actively participate in postpartum uterus remodeling in the mouse, undergoing dynamic changes and contributing to various non-immune endometrial cell populations as part of the process of cellular turnover and regeneration. These observations may have important implications for human uterine physiology and pathological conditions such as postpartum uterine scarring. |
Databáze: | OpenAIRE |
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