Abstract
Despite approaches in regenerative medicine using stem cells, bio-engineered scaffolds, and targeted drug delivery to enhance human tissue repair, clinicians remain unable to regenerate large-scale, multi-tissue defects in situ. The study of regenerative biology using mammalian models of complex tissue regeneration offers an opportunity to discover key factors that stimulate a regenerative rather than fibrotic response to injury. For example, although primates and rodents can regenerate their distal digit tips, they heal more proximal amputations with scar tissue. Rabbits and African spiny mice re-grow tissue to fill large musculoskeletal defects through their ear pinna, while other mammals fail to regenerate identical defects and instead heal ear holes through fibrotic repair. This Review explores the utility of these comparative healing models using the spiny mouse ear pinna and the mouse digit tip to consider how mechanistic insight into reparative regeneration might serve to advance regenerative medicine. Specifically, we consider how inflammation and immunity, extracellular matrix composition, and controlled cell proliferation intersect to establish a pro-regenerative microenvironment in response to injuries. Understanding how some mammals naturally regenerate complex tissue can provide a blueprint for how we might manipulate the injury microenvironment to enhance regenerative abilities in humans. Stem Cells Translational Medicine 2018;7:220–231.
| Original language | English |
|---|---|
| Pages (from-to) | 220-231 |
| Number of pages | 12 |
| Journal | Stem cells translational medicine |
| Volume | 7 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2018 |
Bibliographical note
Publisher Copyright:© 2017 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press
Funding
A.W.S. is supported by the National Science Foundation (NSF) and the Office for International Science and Engineering (OISE) (IOS-1353713) and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS—NIH) (R01AR070313).
| Funders | Funder number |
|---|---|
| National Science Foundation Arctic Social Science Program | |
| National Institutes of Health (NIH) | |
| National Institute of Arthritis and Musculoskeletal and Skin Diseases | R01AR070313 |
| Office of International Science and Engineering | IOS-1353713 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Animal models
- Monocyte
- Tissue regeneration
- Tissue-specific stem cells
ASJC Scopus subject areas
- Developmental Biology
- Cell Biology
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