The guiding hands (and feet)

10 May 2019 | Research
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Focal adhesions in embryonic stem cells

Embryonic stem cells are pluripotent, meaning that they can transform into any cell type in the body depending on the environmental signals (physical or biochemical) that they are exposed to. Like adult cells, embryonic stem cells have specialised molecular apparatus called focal adhesions (FAs) that help in sensing physical signals from their surroundings. Whether and how embryonic stem cell FAs differ in structure and functions compared to FAs in adult cells was explored in a recent study, led by Associate Professor Pakorn Tony Kanchanawong, Principal Investigator at the Mechanobiology Institute (MBI) at the National University of Singapore. This work was published in the journal ACS Biomaterials Science & Engineering earlier this year.

The nanoscale organisation of focal adhesions in embryonic stem cells

The genesis of stem cell therapies is considered a turning point in the field of medicine. With the potential to be transformed into any cell type in the body in the presence of appropriate guidance signals, stem cells could be used to treat a wide range of life-threatening or debilitating diseases, including cancers, diabetes, Parkinson’s, cardiac infarctions, inflammatory disorders, and many more. However, these therapies rely on efficient transformation of stem cells into desired cell types, with transformation potentials depending on multiple factors, including the type of stem cell used: adult or embryonic. This demands a thorough understanding of the various cellular and extracellular factors that might influence the transformation process in each of these two stem cell types.

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Illustration: An artistic depiction of the different mechanosensing capabilities of embryonic stem cell and adult cell focal adhesions. While the large, well-developed focal adhesions (suckers on the tentacles) of the adult cells (red octopus) are highly mechanosensitive and facilitate adherence to their surface strongly, the focal adhesions on embryonic stem cells (blue baby octopuses) are smaller and fewer in number, and are less mechanosensitive, which is depicted here by their inability to hold onto their surfaces strongly.

The role of biochemical signals like growth factors or hormones in influencing stem cell transformation is well known and many of these molecules, alone or in combination, are widely employed to harvest desired cell populations for use in regenerative medicine. The role of physical properties of the cell and its surroundings as important guidance cues has generated tremendous interest in recent years. The idea has found validation through several groundbreaking studies that reveal the direct influence that the physical properties of the tissue can have on stem cell transformation. 

For instance, adult stem cells grown on softer surfaces are known to transform into soft brain tissues while those grown on stiffer surfaces transform into harder bone tissues. While such effects are robust in adult stem cells, how physical signals control embryonic stem cell transformation is not clearly understood.

How embryonic stem cells sense the physical state of their surroundings 

Research has shown that stem cells - much like the adult specialised cells that they transform into - form multiprotein assemblies called focal adhesions (FAs) that are endowed with this special ability. FAs are to cells what hands and feet are to us; FA proteins physically anchor cells to their surfaces and allow cells to feel their surroundings. They are also attached to subcellular structures (actin filaments that form a supportive framework) inside the cell and, therefore, function as channels through which physical signals are transmitted between the inside and outside of a cell.

Differences in FAs in embryonic stem cells and adult specialised cells unclear

Whether the structure and functions of embryonic stem cell FAs are any different from those formed in adult specialised cells (classical FAs), and how these differences influence various physiological processes in stem cells, including their transformation potential is not clear. A group of MBI researchers, led by the Institute’s doctoral student Ms Xia Shumin, along with Assoc Prof Kanchanawong, set out to find some answers by studying FA structure and function in mouse embryonic stem cells.

By using bioinformatics tools, they revealed that embryonic stem cell FAs are similar in composition to classical FAs; the key proteins that form the core of classical FAs were found in embryonic stem cell FAs too. The researchers then used super-resolution imaging to dig deeper into the manner in which these proteins are arranged within the cell. Interestingly, these proteins distributed into well-defined layers in the cell, spanning between the cell surface and the actin cytoskeleton located nearer to the cell core. 

Closest to the cell surface is the signaling layer constituted by proteins that are capable of sensing signals from their environment. The signals are then relayed inside the cell by proteins constituting the force transmission layer. Farthest from the cell surface is the regulatory layer that mediates changes in actin organization in response to incoming signals. Actin reorganisation generates forces, which is channelled back into the surroundings via the FAs.

Interestingly, the researchers noted that the arrangement displayed by embryonic stem cell FA protein was quite similar to the multi-layered organisation of classical FA components that was reported in a previous study from the Kanchanawong Lab at NUS. However, embryonic stem cell FAs looked compressed - their force transmission layer was particularly shorter in length - compared to classical FAs. Furthermore, in stem cells a key FA protein called vinculin moved away from the force transmission layer - where it was prominently distributed in classical FAs - and instead distributed at the regulatory layer in a manner that is dependent on the external environment of the cells.

Variations at the organisational level could influence how FAs function in embryonic stem cells, as embryonic stem cell FAs displayed weaker mechanosensing abilities compared to their counterparts in specialised cells. While classical FAs are known to grow in size in response to increasing stiffness of the surrounding tissues, embryonic stem cell FAs remained small on surfaces of varying stiffness. Based on these findings, the researchers concluded that the compressed force transmission layer in embryonic stem cell FAs is probably responsible for the weakened response of the FAs to the physical state of their surroundings.

How stem cells sense the physical state of their surroundings has a crucial impact on what cell type they transform into as well as on the efficiency of this transformation process. Understanding the role of focal adhesions in this process is important in order to gain deeper insights into the molecular mechanisms involved and to be able to better define experimental parameters that will boost transformation efficiencies. By unraveling the similarities and differences in the composition and molecular organisation of embryonic stem cell FAs relative to classical FAs, the study explains the differences observed in the mechanosensing abilities of these two cell types and offers clues to alter mechanosensing responses through modulations at the molecular level.