Micropatterning of cells reveals chiral morphogenesis
© BioMed Central Ltd 2013
Published: 3 April 2013
Skip to main content
© BioMed Central Ltd 2013
Published: 3 April 2013
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.
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 ; (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 . 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 . 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 . The upper limb malformations associated with Holt-Oram syndrome are also more common on the left side . 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 .
Third, there is a strong correlation between breast cancer and abnormal cerebral asymmetry . 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.
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 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 , 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 . 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 . 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.
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 . 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.
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 , and a directional cell migration along the boundary. Using the same definition of three axes of Xu and colleagues , the CCW alignment on rings can be considered as a cellular 'leftward' bias, and CW as a 'rightward' bias.
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 . 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  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 , 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  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.
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 . 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 . 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 .
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 . 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 .
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.
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.
We gratefully acknowledge NIH support of our work (grant EB002520).