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This article is part of the series Physical influences on stem cells.

Review

Micropatterning of cells reveals chiral morphogenesis

Leo Q Wan1*, Kacey Ronaldson2, Mark Guirguis1 and Gordana Vunjak-Novakovic2*

Author Affiliations

1 Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA

2 Department of Biomedical Engineering, Columbia University, New York, NY 10027, USA

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Stem Cell Research & Therapy 2013, 4:24  doi:10.1186/scrt172


The electronic version of this article is the complete one and can be found online at: http://stemcellres.com/content/4/2/24


Published:3 April 2013

© 2013 BioMed Central Ltd

Abstract

Invariant left-right (LR) patterning or chirality is critical for embryonic development. The loss or reversal of LR asymmetry is often associated with malformations and disease. Although several theories have been proposed, the exact mechanism of the initiation of the LR symmetry has not yet been fully elucidated. Recently, chirality has been detected within single cells as well as multicellular structures using several in vitro approaches. These studies demonstrated the universality of cell chirality, its dependence on cell phenotype, and the role of physical boundaries. In this review, we discuss the theories for developmental LR asymmetry, compare various in vitro cell chirality model systems, and highlight possible roles of cell chirality in stem cell differentiation. We emphasize that the in vitro cell chirality systems have great promise for helping unveil the nature of chiral morphogenesis in development.

Left-right asymmetry in development and disease

Organisms often adopt consistent left-right (LR) asymmetric positioning and morphology of internal organs, a phenomenon known as handedness or chirality. The chirality of biomolecules such as sugar and DNA has been recognized for a long time, but the origins of LR asymmetry in living organisms are not yet well understood. In general, the LR patterning is considered to follow four steps: (i) LR symmetry breaking by orienting the LR axis with respect to the anteroposterior and dorsoventral axes [1]; (ii) transferring initial chiral information into LR positions in a multicellular field; (iii) LR asymmetric expression of signaling molecules; and (iv) asymmetric morphogenesis of visceral organs induced by these molecules [2-4]. Proper LR patterning requires reliable breaking of LR symmetry at early developmental stages as well as the transmission and amplification of LR signals at later stages. Defects in any of the four steps may lead to severe outcomes in laterality. For instance, during the asymmetric gene expression, the midline structure functions as a barrier and keeps left-sided signals from affecting the right side, and vice versa [5]. Midline defects result in disturbances of normal laterality.

Abnormality in LR asymmetry is also closely associated with disease. First, abnormality in LR signaling often leads to malformations, including situs ambiguus (one or more organs in the mirrored position) and situs inversus (all internal organs in mirrored positions). These defects may result from heritable genetic diseases such as Kartagener syndrome, or prenatal exposure to teratogens [6]. Maternal diseases such as diabetes can also trigger laterality defects [7,8].

Second, many diseases are associated with LR asymmetry [9,10]. The incidence of cancer significantly changes with laterality, with stronger occurrence of lung, testis, and ovarian cancer on the right side, and breast cancer and melanoma on the left side [9]. The upper limb malformations associated with Holt-Oram syndrome are also more common on the left side [11]. Detailed analyses showed that the position-dependent incidence of disease may not be necessarily associated with asymmetric organ mass or personal handedness and therefore remains unexplained [12].

Third, there is a strong correlation between breast cancer and abnormal cerebral asymmetry [13]. Altogether, these findings suggest that disease and abnormal LR asymmetry are closely related and may share common developmental origins, whether environmental or genetic [12-15]. Therefore, it is of great scientific interest and clinical significance to investigate the LR asymmetry in development and disease.

We focus on recent in vitro studies of LR asymmetry, within the overall context of LR patterning in development. Starting from the unsolved problems in two current models of LR symmetry breaking, we discuss in vitro studies of cell chirality, and their possible applications in vivo.

LR symmetry breaking in development

The initiation of LR asymmetry in development, also known as LR symmetry breaking, is one of the most intriguing problems in developmental biology. While it is widely believed that LR patterning is ultimately derived from the chirality of biomolecules, the exact mechanism, timing, and location of symmetry breaking are still being debated. The central question is how the biophysical molecular chirality is converted into LR asymmetric gene expression during development. Two important models - the primary cilium model and the voltage gradient model - can each provide an explanation, but they differ about how and when the molecular chirality gives rise to positional information.

In the primary cilium model (Figure 1a), the symmetry breaking is considered to occur at the ventral node at the late neural-fold stage of mouse development. The node cells are well organized and have beating primary cilia on their membranes, which drive a leftward flow, leading to the LR asymmetry of gene expression of Nodal and other proteins [16-18]. The LR asymmetry breaking via primary cilia has three essential characteristics: (i) a consistent posterior tilt of cilia; (ii) synchronized beating; and (iii) unidirectional cilia rotation (that is, in the counterclockwise direction when viewed from the ventral side). The posterior orientation of cilia and concerted beating are believed to relate to the interaction between node cells, possibly through planar cell polarity [19-21]. However, the mechanism by which cilia beat in a unidirectional fashion remains unclear. In addition, evidence suggests that the primary cilia model may not play equally important roles in all cases [22-24].

thumbnailFigure 1. Two models for the initiation of left-right asymmetry in embryo development. (a) Primary cilia model. The cells at the ventral node have their primary cilia position toward the posterior side, while these cilia spontaneously rotate in a counter-clockwise fashion and drive an effective flow toward the left over the node, thus inducing a gradient of morphogens and determining the left-right axis. (b) Voltage gradient model. At the four-cell cleavage stage of a fertilized Xenopus egg, the mRNAs for ion transporter proteins are directionally transported to the right-ventral side, leading to localized asymmetric ion transporter expression and generating a left-right voltage gradient across the ventral midline, inducing sided asymmetric gene expression

In snail, fly, chick and pig, cilia are not present during LR development. In addition, several mutants have abnormal or no ciliary motion, but their LR asymmetric body plan is found to be normal [24-26]. These suggest that ciliary motion is not necessarily required for LR patterning, and that other mechanisms might be responsible for LR symmetry breaking.

A second mechanism involves an electrical voltage gradient (Figure 1b) that transports small LR determinants such as serotonin to one side of the body, where they initiate asymmetric gene expression of Nodal and other proteins. The voltage gradient, determined by asymmetric localization of ion channels, was found as early as the two-cell or four-cell cleavage stages in the Xenopus and chick embryos [27,28]. In addition, cell asymmetric migration at the Hensen's node of chick embryos was found to be a downstream event for transient depolarization of membrane potential on the left side mediated by H+/K+ ATPase activity.

It is believed that the ion channel mRNAs and proteins are directionally transported by the involvement of chiral 'F' molecules so that ion transporters are mostly localized at the right-ventral side. The concept of 'F' molecules was first presented by Wolpert and colleagues [1], and these molecules have three mutually perpendicular axes that follow the anteroposterior axis, the dorsoventral axis, and the LR axis. The nature of the 'F' molecule is largely unknown. A cytoskeletal origin of asymmetry was recently demonstrated by finding the pre-existence of chirality of actin cytoskeleton wrapped around the cortex of Xenopus eggs [29]. In addition, the actin/tubulin network was conjectured to fulfill the function of 'F' molecules, with actin aligned at the bottom and microtubules on the top along the LR direction, with the directional transport along microtubules defining the LR axis [4]. However, this cytoskeleton network model remains to be characterized and validated for the orientation of the LR axis with respect to the other two axes of the early embryo.

In general, the breaking of LR symmetry has been associated with the function of chiral cellular structures, such as the ventral node in mice. Importantly, chiral structures must be organized in a specific fashion so that their collective behavior allows generation of significant biophysical signals that can be translated into local asymmetric gene expression and subsequently amplified into the difference between the LR sides. Two questions are of fundamental interest in this regard: whether chirality is a fundamental property of the cell, and how the chirality of single cells is translated into multicellular chiral morphogenesis. It will be greatly helpful if these questions can be addressed in in vitro systems, where asymmetric biophysical and biochemical cues can be excluded.

In vitro cell chirality

The chirality has been observed in several cellular systems [30-32]. For instance, bacterial colonies can develop chiral morphology with branches twisted in the same handedness [30]. This behavior is believed to be derived from the chirality of the flagella that propel the cell body and induce a defined handedness of rotation. The neurite outgrowth of hippocampal explants has a rightward bias, and turns clockwise on two-dimensional substrates [31,32]. Such turning has been shown to be driven by the autonomous right-screw rotation of growth cone filopodia, possibly through the interactions between myosins (Va and Vb) and filamentous actins.

It was not until recently that intrinsic cell chirality has been studied in a well-controlled and highly repeatable fashion and detected in almost all cell types [33-35]. We will review recent research progress on cell chirality at the levels of single cells as well as multiple cells. In these in vitro systems, no node, cilia or fluid flow is required to establish consistent asymmetry, indicating that chirality is a fundamental intrinsic cellular property.

Chirality at the single cell level was clearly demonstrated by Xu and colleagues [33] through studying the migration of sparsely seeded neutrophil-like differentiated HL-60 (dHL-60) cells (Figure 2). It was found that upon the induction of polarization by a uniform chemo-attractant (f-Met-Leu-Phe (fMLP)), the cells primarily migrated in the direction defined by the axis from the middle of the nucleus to the centrosome, but had a tendency to move toward the left side. The authors proposed that the chiral structure of the centrosome could be responsible for the observed single cell chirality, and that the centrosome could polarize the cell and subsequently determine its directional response to chemical stimuli. The cell chirality could be observed by inducing neutrophils to polarize without creating spatial cues and by studying single cell polarization in conditions free of the effects of neighboring cells. The authors defined cell chirality as either the leftward or rightward bias, with respect to two predefined cellular axes: one axis defined by the cells' attachment to the substrate and the other axis defined by the centrosomes' relation to the nuclei. A leftward bias was observed for dHL-60 cells and found to be microtubule dependent. Inspired from studies in neurons and astrocytes, the Cdc42/Par6 polarity pathway was investigated for specific mechanisms of establishing cell chirality. Upstream disruption of the pathway (that is, interfering Par6, Cdc42, or phosphatidylinositol (3,4,5)-trisphosphate) prevented the establishment of polarity altogether, while downstream disruptions (that is, interfering protein kinase C-ζ or dynein) were only found to randomize the chirality. Surprisingly, constitutive activation of glycogen synthase kinase-3β (GSK3β), located in the middle of the proposed Cdc42/Par6 polarity pathway, was able to reverse the bias of fML P-induced polarity rather than just randomize it. Recently, this system was used to demonstrate the non-ciliary role of microtubule proteins in LR patterning across biological kingdoms [36]. Mutation of tubulin was shown to alter LR patterning in plants, nematodes and frogs, as well ashuman cells in culture.

thumbnailFigure 2. Bias of single cell polarity. The red arrow shown is drawn from the center of the nucleus (blue) to the centrosome (green). Migration to the left of the nucleus-centrosome axis (that is, red arrow) is regarded as leftward bias, typified by the dHL-60 cells (a) and to the right is regarded as rightward bias (b).

The establishment of chirality at a multicellular level has also been related to the intrinsic cell chirality. We previously investigated the establishment of the LR axis by characterizing multicellular alignment and migration in response to micropatterned appositional boundaries (Figure 3) [34,37]. By using micropatterning techniques, a cell monolayer was formed within geometries, which imposed boundary conditions on cells and thus forced them to make the LR decision. A prerequisite to forming this chirality was the geometric imposition of two opposing boundaries within a distance up to several hundred micrometers, such as those found in geometries composed of linear strips and rings but not in square or circle geometries. Primary use of ring geometry allowed for the use of an image-based algorithm, based on the overall alignment of individual cells with respect to the circumferential direction, to determine the multicellular chirality as clockwise (CW) or counter-clockwise (CCW).

thumbnailFigure 3. Left-right asymmetry on micropatterned surfaces. The cells are polarized at the boundary by positioning their centrosomes (green) and Golgi apparatuses (purple) closer to each boundary than nuclei (blue), while forming chiral alignment. (a) Polarity and chirality of muscle cells on micropatterned surfaces. The leftward bias of muscle cells on appositional boundaries creates the observed counter-clockwise (CCW) cell alignment. (b) Schematic of polarity and chirality of endothelial cells on micropatterned surfaces. The rightward bias of cell migration creates the observed clockwise (CW) alignment.

This LR decision was apparent at a multicellular level, and specific to cell phenotype. Most investigated cells (for example, endothelial cells, osteoblasts, adult mesenchymal stem cells, and fibroblasts) displayed a CW bias, except for two myoblast cell lines, derived from mouse and human skeletal muscles, which were found to have a CCW bias. These results suggest that cell chirality might alter during the differentiation of stem cell function. Therefore, it will be necessary to investigate the chirality of the cells relevant to LR asymmetry development, and examine effects of important biochemical and biophysical LR signals.

Investigations into the mechanism behind multicellular chirality revealed the role of actin in the establishment of CCW cell lines, as revealed by the reversal of CCW chirality to CW chirality upon the introduction of actin-interfering drugs. Surprisingly, it was found that microtubule-destabilizing drugs had no effect on the establishment of CCW or CW chirality. Thus, while the establishment of a directional bias is still undetermined, there is a clear role for functional actin in establishing the CCW alignment. In addition, the cells were found to have a consistent polarization, with their centrosome (rather than the nuclei) positioned closely to geometrical boundaries [38], and a directional cell migration along the boundary. Using the same definition of three axes of Xu and colleagues [33], the CCW alignment on rings can be considered as a cellular 'leftward' bias, and CW as a 'rightward' bias.

Recently, Chen and colleagues [35] also were able to observe multicellular chirality at a larger scale (that is, several centimeters) on two-dimensional surfaces through the use of micro-fabrication techniques (Figure 4). They found that culturing vascular mesenchymal cells on substrates containing alternating cell-adhesive coated fibronectin lanes and non-adhesive coated polyethylene glycol lanes resulted in a highly organized chiral pattern. The cells initially attached to fibronectin-coated lanes with a similar chiral alignment found by Wan and colleagues [34], and subsequently expanded to the entire surface with polyethylene glycol degradation, forming a rightward bias of an approximately 20° angle between grooves and aligned cells. The accumulation of stress fibers upon encountering substrate interfaces was speculated to induce mechanical cues that lead to the formation of chiral patterns aligned diagonally to these interfaces. This hypothesis was confirmed in inhibition studies with the nonmuscle myosin-II inhibitor blebbistatin, and the Rho-associated kinase (ROCK) inhibitor Y27632.

thumbnailFigure 4. Propagation of cell chirality with loss of geometric control. Cells preferentially attach to the fibronectin (FN) domain immediately after plating onto alternating fibronectin/polyethylene glycol (PEG) lanes, and they form a biased alignment within the FN domain. With PEG degradation and cell proliferation, the cells migrate out of the FN domain but maintain chirality over the entire surface.

A reaction-diffusion mathematical model was developed to describe possible effects of two morphogens: bone morphogenesis protein (BMP)-2, a slowly diffusing activator, and matrix γ-carboxyglutamic acid protein (MGP), a rapidly diffusing inhibitor of BMP [39]. Within a two-dimensional domain, they created a spatiotemporal gradient of chemicals. The cells were assumed to respond to the gradient of morphogens with a consistent directional bias that was responsible for the chirality of pattern formation. However, it needs to be experimentally validated whether and by which mechanisms these two morphogens can induce a reliable bias relative to the chemical gradient axes.

In summary, all the in vitro cell chirality systems rely on definite cell polarization either transiently determined upon the exposure to chemoattractants, or induced by physical boundaries, and the chirality is detected as a result of biased cell movement in a direction perpendicular to cell polarization. The single cell system [33] presents the first direct demonstration of the existence of chirality of single cells, but it requires cell centrosome and nucleus live imaging and is currently limited to only one cell type, dHL-60. The micropatterning system by Wan and colleagues [34], on the contrary, demonstrated, with a variety of cells in a highly reliable fashion, that multicellular chiral structures can emerge from a homogeneous cell population within well-controlled microscale boundaries. Chen and colleagues [35] further showed that such an initial cell chiral alignment could be propagated into a larger scale if cells are allowed to migrate out of the boundaries. Altogether, these studies suggest that most, if not all, cells are chiral in nature, and single cell chirality can manifest into multicellular chiral morphogenesis with well-controlled boundaries, even at a large scale.

Possible roles of cell chirality in LR asymmetry

All these in vitro cell chirality systems suggest that chiral morphogenesis can be generated without specific embryonic structures such as ventral node or even beating cilia. Most, if not all, cells are intrinsically chiral, just like what was found with Xenopus eggs [29]. Therefore, these in vitro studies provide further support for cytoplasmic models, such as directional transport in fertilized eggs in the voltage gradient model. Furthermore, in vitro studies demonstrate that, under certain conditions, cell chirality will appear as biases in cellular function: migration and alignment. These new findings may provide alternative explanations for LR embryonic development.

We believe that advances in the understanding of cell chirality in in vitro systems could potentially help unveil the mechanism of in vivo LR asymmetry development [37,40]. First, the intrinsic cell chirality may utilize the same cell machinery that is responsible for LR symmetry breaking. The current models for early LR development (that is, nodal flow and voltage gradient) still have essential unanswered questions, which could be addressed by studying cell machinery involved in intrinsic cell chirality. Second, it is possible that the intrinsic cell chirality may contribute to other LR asymmetry events such as heart tube and gut looping, and brain asymmetry [22]. Third, boundaries might direct the establishment of chiral structures. Interestingly, biased cell migration has been found around the Hensen's node (equivalent to the ventral node in mice) in chicken development [41].

Interestingly, drugs regulating cell chirality resemble those affecting LR asymmetry. Actin function was critical for cell chirality on patterned surfaces. Many asymmetric breaking events are related to actin function, such as asymmetric cell division, chiral alignment of embryonic cells at early stages of development, and in vitro actin shear structure induced in the Xenopus egg. In the snail Lymnaea stagnalis, the interference of actin dynamics, but not microtubules, alters the chirality of early dextral embryos [42]. In the hindgut looping of Drosophila, the mutation of myosin ID, an actin motor, was found to reverse chirality of hindgut looping [43-45]. In Caenorhabditis elegans, the LR asymmetry was found to associate with actin and cortical forces and be regulated by non-canonical signaling pathways [46].

The recent progress in the in vitro cell chirality may greatly accelerate research in LR asymmetry during development. An in vitro cell chirality system allows for quick assessment of effects and mechanisms of relevant drugs and growth factors in a well-controlled manner, by excluding possible confounding factors.

However, it is important to point out that it is still not clear when and how cell chirality is exactly utilized during the development. In particular, the cells on a two-dimensional substrate may behave quite differently from those in embryonic development. Cellular microenvironments, including soluble factors and extracellular matrix, need to be better mimicked in in vitro systems [47-49] before they can be utilized in LR asymmetry research in embryonic development.

Conclusion

In vitro cell chirality may create a new paradigm to study the role of intracellular and intercellular machinery in LR asymmetry breaking in development. Whether and to what extent the intrinsic cell chirality can be used to explain the LR asymmetry events are intriguing questions to be addressed in future work.

Note

This article is part of a thematic series on Physical influences on stem cells edited by Gordana Vunjak-Novakovic. Other articles in the series can be found online at http://stemcellres.com/series/physical webcite

Abbreviations

CW: clockwise; CCW: counter-clockwise; dHL-60: differentiated HL-60; fMLP: f-Met-Leu-Phe; LR: left-right.

Competing interests

The authors declare that they have no competing interests; however, Columbia University is applying for a patent related to a technology for measuring cell chirality with micro-patterns.

Acknowledgements

We gratefully acknowledge NIH support of our work (grant EB002520).

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