Out
of their niche environment, adult stem cells, such as mesenchymal
stem cells (MSCs), spontaneously differentiate. This makes both studying
these important regenerative cells and growing large numbers of stem
cells for clinical use challenging. Traditional cell culture techniques
have fallen short of meeting this challenge, but materials science
offers hope. In this study, we have used emerging rules of managing
adhesion/cytoskeletal balance to prolong MSC cultures by fabricating
controllable nanoscale cell interfaces using immobilized peptides
that may be enzymatically activated to change their function. The
surfaces can be altered (activated) at will to tip adhesion/cytoskeletal
balance and initiate differentiation, hence better informing biological
mechanisms of stem cell growth. Tools that are able to investigate
the stem cell phenotype are important. While large phenotypical differences,
such as the difference between an adipocyte and an osteoblast, are
now better understood, the far more subtle differences between fibroblasts
and MSCs are much harder to dissect. The development of technologies
able to dynamically navigate small differences in adhesion are critical
in the race to provide regenerative strategies using stem cells.
Major design aspects for novel biomaterials are driven by the desire to mimic more varied and complex properties of a natural cellular environment with man-made materials. The development of stimulus responsive materials makes considerable contributions to the effort to incorporate dynamic and reversible elements into a biomaterial. This is particularly challenging for cell-material interactions that occur at an interface (biointerfaces); however, the design of responsive biointerfaces also presents opportunities in a variety of applications in biomedical research and regenerative medicine. This review will identify the requirements imposed on a responsive biointerface and use recent examples to demonstrate how some of these requirements have been met. Finally, the next steps in the development of more complex biomaterial interfaces, including multiple stimuli responsive surfaces, surfaces of 3D objects and interactive biointerfaces will be discussed.
In culture isolated bone marrow mesenchymal stem cells (more precisely termed skeletal stem cells, SSCs) spontaneously differentiate into fibroblasts, preventing the growth of large numbers of multipotent SSCs for use in regenerative medicine. However, the mechanisms that regulate the expansion of SSCs, while maintaining multipotency and preventing fibroblastic differentiation are poorly understood. Major hurdles to understanding how the maintenance of SSCs is regulated are (a) SSCs isolated from bone marrow are heterogeneous populations with different proliferative characteristics and (b) a lack of tools to investigate SSC number expansion and multipotency. Here, a nanotopographical surface is used as a tool that permits SSC proliferation while maintaining multipotency. It is demonstrated that retention of SSC phenotype in culture requires adjustments to the cell cycle that are linked to changes in the activation of the mitogen activated protein kinases. This demonstrates that biomaterials can offer cross-SSC culture tools and that the biological processes that determine whether SSCs retain multipotency or differentiate into fibroblasts are subtle, in terms of biochemical control, but are profound in terms of determining cell fate.
Nanotopographical cues observed in vivo (such as in the sinusoid and bone) closely resemble nanotopographies that in vitro have been shown to promote niche relevant stem cells behaviours; specifically, retention of multipotency and osteogenic differentiation on ordered and disordered nano-pits respectively. These and other observations highlight a potential role for nano topography in the stem cell niche.
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