Biological Effects of Culture Substrates on Human Pluripotent Stem Cells

Hayashi, Yohei; Furue, Miho Kusuda

doi:https://doi.org/10.1155/2016/5380560

Stem Cells International

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Review Article | Open Access

Volume 2016 | Article ID 5380560 | https://doi.org/10.1155/2016/5380560

Biological Effects of Culture Substrates on Human Pluripotent Stem Cells

Yohei Hayashi¹and Miho Kusuda Furue²

Academic Editor: Raymond Ching-Bong Wong

Received28 Apr 2016

Accepted04 Jul 2016

Published30 Aug 2016

Abstract

In recent years, as human pluripotent stem cells (hPSCs) have been commonly cultured in feeder-free conditions, a number of cell culture substrates have been applied or developed. However, the functional roles of these substrates in maintaining hPSC self-renewal remain unclear. Here in this review, we summarize the types of these substrates and their effect on maintaining hPSC self-renewal. Endogenous extracellular matrix (ECM) protein expression has been shown to be crucial in maintaining hPSC self-renewal. These ECM molecules interact with integrin cell-surface receptors and transmit their cellular signaling. We discuss the possible effect of integrin-mediated signaling pathways on maintaining hPSC self-renewal. Activation of integrin-linked kinase (ILK), which transmits ECM-integrin signaling to AKT (also known as protein kinase B), has been shown to be critical in maintaining hPSC self-renewal. Also, since naïve pluripotency has been widely recognized as an alternative pluripotent state of hPSCs, we discuss the possible effects of culture substrates and integrin signaling on naïve hPSCs based on the studies of mouse embryonic stem cells. Understanding the role of culture substrates in hPSC self-renewal and differentiation enables us to control hPSC behavior precisely and to establish scalable or microfabricated culture technologies for regenerative medicine and drug development.

1. Introduction

Human pluripotent stem cells (hPSCs) have the unique features of self-renewal and pluripotency. These features give rise to the unprecedented potential of advancing regenerative medicine, drug development, and human biology. Two types of hPSCs are widely used; human embryonic stem cells (hESCs) were derived from the inner cell mass (ICM) of the blastocyst [1], and human induced pluripotent stem cells (hiPSCs) were generated by introducing key transcription factors into somatic cells [2, 3]. There have been numerous arguments for differences between hESCs and hiPSCs; however, both hESCs and successfully-reprogrammed hiPSCs generally have similar gene expression patterns, differentiation potentials, and epigenetic signatures [4–6].

To utilize hPSCs in industrialized regenerative medicine and drug development, the culture methods must be improved to meet the technological standards in safety, cost-effectiveness, and the easiness of handling. Early culture methods for hPSCs were similar to the methods developed for mouse embryonic stem cells (mESCs) [7, 8]. The methods employed coculturing hPSCs with irradiated or mytomicin-C-treated mouse embryonic fibroblasts (MEF) or immortalized embryonic fibroblast lines (e.g., STO or SNL cell lines) as feeder cells in culture media containing fetal calf serum (FCS) or serum replacement (SR). Since these feeder cells, FCS, or SR provide undefined attachment factors for cultured cells, specific culture substrates except for gelatin, which are hydrolyzed and denatured collagens, are not generally required. Since feeder cells, FCS, or SR also contain undefined, xenogenic allergens, these components must be carefully audited for animal-derived raw material controls in compliance with regulation in applying to regenerative medicine. Besides, using feeder cells practically caused many troubles, such as cellular cross-contamination, the lack of reproducibility, or time-consuming preparation.

To overcome these problems, feeder-free culture methods have been developed. The first study used the conditioned medium of MEF feeder cells in 2001 [9]. In 2004-2005, subsequent studies used the high concentration of SR or other crude extracts supplemented with recombinant cytokines and/or chemicals [10–13]. Since 2005, defined culture media for hPSCs have been developed [14–18]. In these culture media, the most common cytokine is bFGF, which activates MAPK and/or PI3K-AKT signaling pathways. The second is Nodal/Activin/TGFβ, which activate TGFβ-SMAD signaling pathway. Activation of these signaling pathways is critical to maintain hPSC self-renewal [15, 19]. Defined culture media enable us to identify other cytokines and chemicals which promote hPSC self-renewal and/or single-cell survival (e.g., heparin [20], albumin-associated lipids [21], pleiotrophin [22], and IGF1 analog and heregulin-1β (a ligand for ERBB2/ERBB3) [23]). Extracellular Matrix (ECM) proteins and other culture substrates can be also effectively examined using defined culture media.

Here we summarize the application of various ECM proteins and other types of culture substrates to defined hPSC culture media. Further, we will discuss the functional roles of signaling pathways under integrins, which are major receptors for ECM proteins. Last, we will discuss the possible effect of culture substrates on naïve hPSCs, which exhibit the different biological state of pluripotency; although conventional (or called “primed”) embryonic or induced pluripotent stem cells cannot create chimeric animals by the blastocyct injection, naïve pluripotent stem cells can create them. Naïve and primed pluripotent stem cells have distinct gene expression patterns and signal dependencies [24].

2. Role of Culture Substrates in hPSCs

Although some studies have applied suspension culture to hPSCs [25–27], hPSCs are usually regarded as anchorage-dependent cells onto which culture substrates are required to support for their survival and growth in vitro. hPSCs do not attach to normal glass, plastics, or agars, which are conventionally used for general cell culture, requiring specific ECM and other proteins, peptides, or synthetic polymers as culture substrates. Here we list the culture substrates used for maintaining hPSC self-renewal in defined culture medium in Table 1. We describe the examples and effects of each culture substrate below.

3. Crude Extracts Secreted by Engelbreth-Holm-Swarm (EHS) Mouse Sarcoma Cells

Since the first report of feeder-free culture conditions of hESCs [9], crude extracts from gelatinous protein mixture secreted by Engelbreth-Holm-Swarm (EHS) mouse sarcoma cells have been widely used to maintain hPSC self-renewal [28]. These extracts are commercially named as Matrigel (Corning), Cultrex BME (Trevigen), or Geltrex (Thermo Fisher Scientific), containing laminin, entactin, collagens and heparin sulfate proteoglycan, and several growth factors. Since these extracts are incompletely defined, they lead to a lot of differences and variable experimental results, making difficult to define growth factor requirements for undifferentiated growth or directed differentiation [35]. Since these extracts are not xeno-free, they must be carefully audited for animal-derived raw material controls in compliance with regulation in applying to regenerative medicine. Thus, specific ECM proteins and other synthetic culture substrates have been commonly used in recent years.

4. Laminin

Laminin is a heterotrimeric protein composed of α, β, and γ-chains. Isoforms of α, β, and γ-chains are found in five, four, and three genetic variants, respectively. The laminin subtypes are named according to their chain composition [53]. For example, laminin-511 consists of α5, β1, and γ1 chains. In the first demonstration of the feeder-free culture conditions of hESCs, the authors compared Matrigel, laminin, collagen IV, and fibronectin to hESC self-renewal [9]. They found that laminin and Matrigel support more undifferentiated hESC colonies than fibronectin or collagen IV. Subsequently, several studies examined each laminin subtype for hPSCs attachment and self-renewal. A study showed that hPSCs adhered to recombinant human laminin-332, laminin-511, and laminin-111 and these laminin isoforms were good substrates to expand undifferentiated hESCs [29]. Another study compared adhesion properties of laminin-511, laminin-332, laminin-411, laminin-111, Matrigel, or Poly-D-Lysine substrates and showed that hESCs adhered to laminin-511 significantly better than to the other substrates [30]. Several studies showed that recombinant laminin-521 successfully maintained hPSC self-renewal for long-term culture [31, 32]. Recently, recombinant E8 fragments of laminin-511 or laminin-521 (LM-E8s), which were the minimum fragments conferring integrin-binding activity, were developed [33]. These fragments adhered to hESCs and hiPSCs better than Matrigel and intact laminin isoforms and sustained long-term self-renewal of hESCs and hiPSCs in defined xeno-free media (tested in mTeSR1 (Stem Cell Technologies), StemPro (Thermo Fisher Scientific), StemFit (Ajinomoto), and serum-free medium supplemented with N2 and B27 supplemants (Thermo Fisher Scientific)) with dissociated cell passaging [34]. Although each study showed slight different results due to the preparation methods and hPSC lines, recombinant laminin-511 and laminin-521 E8 fragments seem to be the most efficient, defined culture substrates for undifferentiated hPSCs so far [53].

5. Other ECM Proteins

Other than laminin, several ECM proteins have been shown to support hPSC self-renewal. Vitronectin is a ECM glycoprotein of the hemopexin family and is found abundantly in serum and bone [54]. Several studies showed that vitronectin robustly supported long-term self-renewal in hPSCs for long-term culture [35–38]. Recombinant truncated vitronectin (VTN-N), which lacked N-terminal Somatomedin B domain, was designed for use with Essential 8 defined medium (Thermo Fisher Scientific or Stem Cell Technologies) and supported human pluripotent stem cell attachment and survival better than wild type vitronectin [39].

Fibronectin is a ECM glycoprotein widely expressed by multiple cell types and is critically important in vertebrate development [55]. Fibronectin also was shown to support long-term self-renewal of hPSCs in several independent studies [40–42], although some unsuccessful results in which fibronectin cannot maintain long-term hPSC self-renewal were reported [9, 35]. This discrepancy might be due to the differences of source, purification methods, or coating methods.

Type I collagen is the most abundant collagen of the human body which forms large, eosinophilic fibers known as collagen fibers [56]. Type I collagen also has been shown to support sustained self-renewal and pluripotency of hPSCs in several independent studies [20, 43]. To our knowledge, the application of other natural ECM proteins has not been reported. Some other reports developed, engineered, or modified ECM proteins to support hPSC self-renewal. A study developed a nanofibrous gelatin substrate with optimal conditions (i.e., density, solution composition, molecular weight, diameter, and crosslink time), although normal gelatin cannot support hESC attachment and growth in defined culture conditions [44]. The authors adjusted the nanofibrous gelatin with 4.6 µg/cm², Acetic Acid : Ethyl Acetate = 3 : 2 as the solution composition, 30 kDa as the molecular weight, 280 nm diameter, and 4 hours of crosslink to support hPSC culture. The adjusted nanofibrous gelatin substrate maintained hPSC self-renewal for a long-term culture. Another study developed a customized recombinant spider silk matrix protein, which was produced in Escherichia coli and can be assembled into mechanically robust films or up to meter-long fibers under nondenaturing and sterile conditions, was fused with peptide motif (i.e., PQVTRGDVFTM) from vitronectin [45]. This xeno-free recombinant protein-based substrate allowed long-term culture of undifferentiated hPSCs.

6. Synthetic Substrates

Other than natural or recombinant proteins, some synthetic materials have been developed to maintain hPSC self-renewal. Synthetic peptide-acrylate surfaces (PAS), which supported self-renewal of hESCs in chemically defined, xeno-free medium, were developed [46]. These surfaces are commercially sold as Synthemax (Corning), which has a synthetic surface composed of RGD (Arg-Gly-Asp) containing short peptides covalently immobilized on acrylate coating to mimic the natural cell environment. The first fully defined synthetic polymer coating, which maintained long-term growth of hESCs in different culture media, was poly[2-(methacryloyloxy)ethyl dimethyl-(3-sulfopropyl)ammonium hydroxide] (PMEDSAH) [47]. Another study developed synthetic substrates displaying heparin-binding peptides, which can interact with cell-surface glycosaminoglycans, showing that synthetic substrates that recognize cell-surface glycans can facilitate the long-term culture of pluripotent stem cells [48]. Another study developed polyvinylalcohol-co-itaconic acid hydrogels grafted with an oligopeptide derived from vitronectin (KGGPQVTRGDVFTMP) with elasticities ranging from 10.3 to 30.4 kPa storage moduli by controlling the crosslinking time [49]. The hPSCs cultured on the stiffest substrates (30.4 kPa) tended to differentiate after five days of culture, whereas the hPSCs cultured on the optimal elastic substrates (25 kPa) maintained their pluripotency for over 20 passages under xeno-free conditions. These results indicate that cell culture matrices with optimal elasticity can maintain the pluripotency of hPSCs in culture. Another study used monomers with high acrylate content, which had a moderate wettability and employed integrin αvβ3 and αvβ5 complexes engagement with adsorbed vitronectin, to promote colony formation [57]. The same group developed UV/ozone radiation modification of typical cell culture plastics to define a favorable surface environment for hPSC culture [50]. Another group developed a synthetic polymer interface made of hydrogel interfaces of aminopropylmethacrylamide (APMAAm) for the long-term self-renewal of human embryonic stem cells (hESCs) in defined media [51]. As the hPSCs are used in industrial and clinical applications more often, the development of defined synthetic culture substrate for hPSCs will be accelerated [47, 58]. Synthemax substrates are widely distributed; however, some of the other methods are hard to be reproduced due to the lack of availability.

7. E-Cadherin

E-cadherin, a Ca²⁺-dependent cell-cell adhesion molecule [59], is essential for intercellular adhesion and colony formation of hPSCs [60]. A study showed that human E-cadherin-Fc chimeric protein as a culture substrate could support the self-renewal of hESCs using completely defined culture conditions [52]. Another group showed that the combination of laminin-521 and E-cadherin Fc chimera proteins allowed clonal derivation, clonal survival, and long-term self-renewal of hPSCs under completely chemically defined conditions without ROCK inhibitors [31]. Also, the laminin-521/E-cadherin matrix allowed hESC derivation from blastocyst and single blastomere cells without a need to destroy the embryo. The use of E-cadherin proteins as culture substrates is a quite interesting method; however, the differences of gene expression, epigenetic modifications, and signaling status between normal ECM-based substrates and E-cadherin-based substrates are still unknown.

8. Endogenous ECM Protein Production in hPSCs

Regarding the endogenous extracellular matrix production of hPSCs, an earlier study using immunostaining methods indicated that all the ECM proteins tested in the study (i.e., firbronectin, laminin, collagen I, collagen IV, or vitronectin) were produced by only feeders or differentiated hPSCs, but not by undifferentiated hPSCs [35]. However, Miyazaki et al. showed that laminin-511 and/or laminin-521 were the most abundant laminin subtype expressed in hPSCS, using immunostaining and RT-PCR methods [29]. Another study showed that undifferentiated hESCs expressed a specific subtype of laminin-511, nidogen-1, and type IV collagen, using immunostaining and RT-PCR methods [61]. To our knowledge, the physiological roles of endogenous nidogen-1 and type IV collagen in hPSCs are still unknown. A recent study examined the production of laminin α5 subunit, type I collagen, fibronectin, or vitronectin in undifferentiated hPSCs and showed that only laminin α5 subunit was produced, using immunostaining method [62]. Taken together, undifferentiated hPSCs surely produce laminin-511 and/or laminin-521, and the production of other ECM proteins is doubtful or unexamined.

A recent study also showed that the disruption of endogenous α5 laminin subunit expression dramatically impaired self-renewal and increased apoptosis and that the impaired self-renewal and survival were restored by culturing on exogenous laminin-521, but not on Synthemax or vitronectin [62]. Another study also showed that the knocking down of laminin α5 in hESCs resulted in the reduction of integrin α6 (ITGA6) and Sox2 mRNA expression and OCT4 protein expression [63]. During differentiation, the expression pattern of laminin isoforms in hPSCs dramatically changes [64]. Together, these studies demonstrated that the endogenous laminin α5 expression, which forms laminin-511 or laminin-521 complexes, was specific and crucial in hPSC self-renewal and survival and that the endogenous laminin production could be substituted by the exogenous deposition of laminin-511 or laminin-521, but not by the other ECM proteins. The requirement of endogenous laminin production in hPSCs implied that the laminin could be functional to support hPSC self-renewal and survival even when other ECM proteins or other materials were used as culture substrates.

9. Expression Patterns and Physiological Roles of Integrin Receptors in hPSCs

Integrins are the major receptors for cell adhesion to ECM proteins, consisting of the heterodimers of the α and β subunits. Each heterodimer attaches to specific ECM proteins differently [65]. Integrin expression patterns in hPSCs have been examined in several studies. The first report of feeder-free culture conditions showed that hESCs expressed high levels of α6 and β1, moderate levels of α2, and low levels of α1, α3, and β4 integrin subunits [9]. These results suggested that the laminin-specific receptor (i.e., α6β1 integrin complex) was important for interacting hESCs with laminin. Consistent with this report, several studies, which used laminin or its fractions as culture substrates, showed that α6β1 integrin complex majorly mediates hPSC adhesion onto laminin [30, 35, 61, 66]. Another report, which used vitronectin as culture substrates, showed that αVβ5 integrin, not α6β1 integrin, mediated hPSC adhesion to vitronectin [35]. Another study showed that αVβ5 integrin was required for initial attachment onto vitronectin, but the inhibition of both αVβ5 and β1 subunits was required to decrease iPSC proliferation significantly [37]. Another report, which used Matrigel as culture substrates, showed that αVβ3, α6, β1, and α2β1 integrins played a significant role in the initial adhesion of the hESCs [67]. Another study showed that hiPSCs grown on the Synthemax surface primarily utilize αVβ5 integrin to mediate attachment to the substrate, whereas multiple integrins were involved in cell attachment to Matrigel [68]. A recent study showed that the knockdown of integrin α6 in hESCs led to a reduction in NANOG, OCT4, and SOX2 levels, suggesting that integrin signaling may be crucial for maintaining hPSC self-renewal and the expression of pluripotency transcription factors [63]. Together, the laminin-specific integrin α6β1 complex must be crucial for hPSC self-renewal and survival. Other integrin complexes, such as αVβ5, αVβ3, and α2β1, which interact with vitronectin, fibronectin, or collagens, may be used for hPSC attachment; however, their physiological roles in hPSC self-renewal remain elusive. It will be interesting and important to examine the role of each integrin subunit in undifferentiated hPSCs by disrupting these genes.

Other than integrins, one study demonstrated that blockage of CD44, which interacts with hyaluronic acid, inhibited cell attachment in 21% O₂ culture conditions [69]. The expression patterns and the physiological roles of other nonintegrin receptors for ECM (e.g., syndecan interacted with fibronectin and other proteins, dystroglycan interacted with laminin, or urokinase-type plasminogen activator receptor interacted with vitronectin) remain elusive.

10. Integrin Signaling on hPSC Self-Renewal

Molecular mechanisms mediating these culture substrates and hPSC self-renewal have been recently started to be uncovered. Generally, integrins transmit their signals via intracellular signaling proteins, such as integrin-linked kinase (ILK) and focal adhesion kinase (FAK). ILK was shown to mediate integrin signals to AKT signaling pathway, and this signaling pathway had an antagonistic effect on endoderm differentiation [70]. Other several studies showed that the activating AKT signaling promoted self-renewal and survival of hPSCs [31, 71–74]. Another study showed that soluble angiopoeitin-1 (Ang-1-) derived peptide QHREDGSQHREDGS, which interacted with β1 integrin, decreased hPSC apoptosis after the single-cell dissociation and that the interaction of the peptide increased ILK expression [75]. On the other hand, a recent study showed that the integrin-FAK signaling pathway was not active in undifferentiated hPSCs [63]. FAK was not phosphorylated at Y397 and was localized in the nuclei of hPSCs, interacting with OCT4 and SOX2. During differentiation, however, integrin α6 levels diminished, and Y397 FAK was phosphorylated. Together, these findings suggested that the integrin-ILK signaling pathway was active in order to maintain hPSC self-renewal and survival through the activation of AKT signaling pathways and that integrin-FAK signaling pathway was not active. The role of the unphosphorylated, nuclear FAK in hPSC on self-renewal should be uncovered in future.

hPSC survival from single cell is usually hard without specific chemical treatment, such as ROCK inhibitors or genetic modification [76, 77]. A recent study showed that the disruption of endogenous α-5 laminin production caused hPSC apoptosis and that the treatment of the laminin α5-deficient cells with blebbistatin or a Rho-associated kinase (ROCK) inhibitor partially restored their self-renewal and diminished apoptosis [62]. These findings implied that ECM-integrin signaling might modulate the status of the Rho-ROCK-Myosin pathway, which was considered as a major player in antiapoptosis of single-cell dissociated hPSCs [78–81]. It will be interesting to reveal the cross-talk effect of ECM-integrin signaling with these antiapoptosis pathways in hPSCs. Together, we illustrate the possible schemes of integrin signaling on self-renewal and single-cell survival of hPSCs from the recent studies described above (Figure 1).

11. Toward Naïve Pluripotent Stem Cells: Perspectives from Mouse Pluripotent Stem Cells

Although conventional hPSCs in bFGF-dependent culture conditions have been widely used, an alternative pluripotent state with different signal dependence has attracted much attention. The derivation of mouse epiblast stem cells (mEpiSCs) clarified that pluripotency contained two developmental stages [82, 83]. mESCs derived from preimplantation inner cell mass represent the “naïve” stage, and mEpiSCs derived from the postimplantation epiblast represent the “primed” stage. mESC self-renewal has been achieved through exposure to the leukemia inhibitory factor (LIF) [84, 85]. We also confirmed the effect of LIF on mESC self-renewal in defined culture conditions [86]. The addition of extracellular signal-regulated kinase (MEK) and glycogen synthase kinase 3 (GSK3) inhibitors (2i) in defined medium allowed the cells to attain a homogeneous ground state [87]. On the other hand, mEpiSCs are cultured in a medium containing bFGF and Activin/Nodal/TGFβ, which is similar to hESCs culture medium. Although some early studies used LIF in feeder-free media for undifferentiated hESCs [11, 88], LIF and its downstream STAT3 signaling pathway were shown to be dispensable for maintaining primed human and primate PSC self-renewal in several independent studies [89–91]. Thus, defined hPSC culture media today usually do not contain LIF; however, reported media for naïve hPSC contain LIF, not bFGF [92–94]. STAT3 activation was reported to be crucial in reprogramming human PSCs to naïve state [95]. A recent study also showed that LIF promoted X chromosome reactivation, which was one of the characteristics of naïve pluripotency in female hPSCs [96]. These studies indicated that naïve hPSCs required different culture conditions and signaling activation status from primed hPSCs. From the similarity of the cytokine requirement and signal dependence, conventional hPSCs represent primed state, similar to mEpiSCs.

The effect of culture substrates on establishing and maintaining naïve hPSC self-renewal is still ill-defined since most of the studies still used feeder cells [92, 93]. Since the colony morphologies of naïve and primed hPSCs are considerably different (i.e., primed hPSCs form flattened colonies, whereas naïve hPSCs form dome-like 3D colonies as mESCs do), the effect of culture substrates in primed and naïve hPSCs might be different. In order to predict the respective effect of different substrates on naïve versus primed state PSCs, we introduce the findings of our previous study using mESCs in defined culture conditions [86]. We revealed that type I collagen, gelatin, or suspension were suitable to maintain mESC self-renewal and that the integrin signaling was inactivated in these conditions [97]. Conversely, laminin or fibronectin induced mEpiSC-like properties, which was featured by altered morphologies, the decreased activity of alkaline phosphatase, increased Fgf5 expression, and decreased Nanog expression. mESC expressed integrins against laminin and fibronectin, and the ECM-integrin signaling promoted differentiation into the primed state from mESCs. From the similarity between mESCs and naïve hPSCs, our findings suggest that type I collagen, gelatin, or suspension, but not laminin or fibronectin, could support naïve hPSC self-renewal and that the suppression of ECM-integrin signaling might also support the features of naïve hPSCs. It will be interesting to test the effect of different ECM proteins on human naïve pluripotency in defined culture conditions.

Examining endogenous ECM and integrin expression in naïve hPSCs and their effect on inducing and maintaining naïve pluripotency should be also interesting. As mentioned above, primed hPSCs express laminin-511 and/or laminin-521 and their receptors, integrin α6β1. However, unlike the mouse equivalent, human ICM cells lacked appreciable laminin expression [98]. Thus, there will be a possibility that naïve hPSCs might have different expression patterns of ECM proteins and integrins from primed hPSCs.

12. Culture Substrates Enable Controlled hPSC Differentiation

Specific culture substrates should be useful to establish efficient and robust differentiation methods. However, the effect of each material on the differentiation into specific cell types has been largely unknown yet. We introduce some of the studies to enhance the utility of specific culture substrates for inducing and maintaining specific cell types.

12.1. The Effect of Culture Substrates on Neural Differentiation from hPSCs

A study used defined adherent culture system to examine the effect of ECM molecules on neural differentiation of hESCs. hESC-derived differentiating embryoid bodies were plated on Poly-D-Lysine (PDL), PDL/fibronectin, PDL/laminin, type I collagen, or Matrigel in neural differentiation medium [99]. They found that neural progenitor, neuronal generation, and neurite outgrowth were significantly greater on PDL/laminin and Matrigel substrates than on other three substrates. The laminin/PDL-induced neural progenitor expansion was partially blocked by the antibody against integrin α6 or β1 subunits. Another study showed that vitronetin was expressed in the ventral part of the developing human spinal cord and profoundly promoted the derivation of oligodendrocyte progenitors that proliferated and differentiated into oligodendrocytes in response to mitogenic and survival factors [100]. These results supported the beneficial effect of vitronectin on oligodendrocytic differentiation of hESCs. Several study showed that specific synthetic polymers or peptides enhanced the proliferation and differentiation of hPSC-derived neural precursors or neurons. Polydopamine coating facilitated highly efficient, simple immobilization of neurotrophic growth factors and adhesion peptides onto polymer substrates. The growth factor or peptide-immobilized substrates greatly enhanced the differentiation and proliferation of human neural stem cells (NSCs: human fetal brain-derived NSCs and human induced pluripotent stem cell-derived NSCs) [101]. Polycaprolactone fiber matrices of different diameter (i.e., nanofibers and microfibers) and orientation (i.e., aligned and random) coated with poly-L-ornithine/laminin were developed to support the adhesion, viability, and differentiation of NSCs [102]. A synthetic polymer, poly(4-vinyl phenol) (P4VP) supported the long-term proliferation and self-renewal of hNPCs [103]. Another study showed that compliant polyacrylamide (PA) hydrogels (~0.7 kPa) functionalized with a glucosaminoglycan-binding peptide inhibited promoted highly efficient differentiation from hPSCs into postmitotic neurons even in the presence of soluble pluripotency factors [104]. Similarly, the neural induction and caudalization of hPSCs were accelerated by a synthetic microengineered substrate, consisting of soft poly-dimethylsiloxane micropost arrays (PMAs) [105].

12.2. The Effect of Culture Substrates on Endodermal Differentiation from hPSCs

A study examined the effect of ECM combinations and concentrations on the differentiation from several hPSC lines into definitive endoderm (DE), an early embryonic cell population fated to give rise to internal organs, such as the lung, liver, pancreas, stomach, and intestine [106]. From this screen, they identified fibronectin and vitronectin as ECM components that promoted DE differentiation. Analysis of integrin expression revealed that differentiation toward DE led to an increase in fibronectin-binding integrin α5 (ITGA5) and vitronectin-binding integrin αV (ITGAV). Another study also showed that DE highly expresses the integrins αV and β5, which have the ability to bind to vitronectin, whilst the expression of the pluripotency related laminin-binding integrin α3, α6, and β4 subunits was downregulated [107]. These studies indicated that ECM compatibility and integrin expression patterns changed dynamically during hPSC differentiation. During later differentiation stages toward hepatocytes, another study showed that hPSC-derived hepatoblast-like cells were maintained for more than 3 months with the ability to differentiate into both hepatocyte-like cells and cholangiocyte-like cells by culturing on the laminin-111-coated dishes [108]. On the other hand, laminin-411 and laminin-511 promoted the cholangiocyte differentiation from hepatoblast-like cells derived from hiPSCs [109]. These results showed that the difference of laminin isoforms distinguished stem cell behaviors and that specific culture substrates enabled controlling stem cell maintenance and differentiation precisely.

13. Application of Culture Substrates from Microfabrication to Scalable Culture Systems

Defined culture conditions with specific culture substrates should be useful to establish various scale culture technologies with specific research purposes. Indeed, a study showed that defined culture conditions enabled microfluidic perfusion culture system for hiPSCs that uses a microchamber array chip under defined ECM proteins and culture medium conditions and that fibronectin and laminin were appropriate for microfluidic devices made out of the most popular material, polydimethylsiloxane (PDMS), by screening various ECM proteins [110]. The same group also demonstrated that the differences of vitronectin and γ-globulin adsorption enabled patterning a PDMS surface with hPSCs [111]. Conversely, toward the development of scalable culture system of hPSCs for regenerative medicine or large-scale drug development, cost-effective, defined, and reproducible culture systems must be required. In these culture systems, the development of suitable culture substrates is critical. Compared with extracted ECM proteins, recombinant proteins and synthetic polymers have advantages in the application of these scalable culture systems.

14. Conclusions

As the clinical application and industrial usage of hPSCs have been advanced, numerous culture media and substrates are now being actively developed. However, some of these culture media and substrates lack the studies of the effect on cellular physiology including cellular signal status, genomic integrity, gene expression profile, or epigenetic status. So far, recombinant laminin-511 or laminin-521 proteins (or their fragments) as the culture substrates and their integrin α6β1 receptor complex seem to be most examined and to have critical roles in maintaining hPSC self-renewal. As the downstream signaling of integrin, ILK activation must be critical in maintaining hPSC self-renewal; however, the molecular mechanisms in general remain elusive. To establish reproducible and stable culture conditions to maintain hPSC self-renewal toward safe clinical application or robust drug screening from hPSCs, detailed studies on molecular mechanisms should be required to control hPSC behavior precisely. After accomplishing these studies, various culture applications from microfabrication to scalable culture of hPSC should be achieved.

Disclosure

The funding bodies had no role in study design, data collection and analysis, decision to publish, or preparation of the paper.

Competing Interests

Yohei Hayashi declares that there are no competing interests regarding the publication of this paper. Miho Kusuda Furue is an inventor of ESF7 and hESF9, which are defined medium for mouse and human pluripotent stem cells, respectively.

Acknowledgments

This work was supported in part by grants from the Ministry of Health, Labor, and Welfare of Japan and Japan Agency for Medical Research and Development (AMED) to Miho Kusuda Furue and the Ministry of Education, Culture, Sports, Science and Technology of Japan to Miho Kusuda Furue (JSPS KAKENHI).

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