Xue Wen, Lee Donghee, Kong Yunfan, Kuss Mitchell, Huang Ying, Kim Taesung, Chung Soonkyu, Dudley Andrew T, Ro Seung-Hyun, Duan Bin
College of Biological Science and Medical Engineering, Donghua University, Shanghai 201620, China.; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.; Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.
Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.; Department of Surgery, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.
Adv Funct Mater. 2023 Aug 29;33(35). doi: 10.1002/adfm.202214129. Epub 2023 Jun 2.
Porous alginate hydrogels possess many advantages as cell carriers. However, current pore generation methods require either complex or harsh fabrication processes, toxic components, or extra purification steps, limiting the feasibility and affecting the cellular survival and function. In this study, a simple and cell-friendly approach to generate highly porous cell-laden alginate hydrogels based on two-phase aqueous emulsions is reported. The pre-gel solutions, which contain two immiscible aqueous phases of alginate and caseinate, are crosslinked by calcium ions. The porous structure of the hydrogel construct is formed by subsequently removing the caseinate phase from the ion-crosslinked alginate hydrogel. Those porous alginate hydrogels possess heterogeneous pores around 100 μm and interconnected paths. Human white adipose progenitors (WAPs) encapsulated in these hydrogels self-organize into spheroids and show enhanced viability, proliferation, and adipogenic differentiation, compared to non-porous constructs. As a proof of concept, this porous alginate hydrogel platform is employed to prepare core-shell spheres for coculture of WAPs and colon cancer cells, with WAP clusters distributed around cancer cell aggregates, to investigate cellular crosstalk. This efficacious approach is believed to provide a robust and versatile platform for engineering porous-structured alginate hydrogels for applications as cell carriers and in disease modeling.
多孔海藻酸盐水凝胶作为细胞载体具有许多优点。然而,目前的造孔方法要么需要复杂或苛刻的制造工艺、有毒成分,要么需要额外的纯化步骤,这限制了其可行性,并影响细胞的存活和功能。在本研究中,报道了一种基于双相水乳液制备高度多孔且负载细胞的海藻酸盐水凝胶的简单且对细胞友好的方法。预凝胶溶液包含海藻酸盐和酪蛋白酸盐两种不混溶的水相,通过钙离子交联。水凝胶构建体的多孔结构是通过随后从离子交联的海藻酸盐水凝胶中去除酪蛋白酸盐相而形成的。那些多孔海藻酸盐水凝胶具有约100μm的异质孔和相互连接的通道。与无孔构建体相比,封装在这些水凝胶中的人白色脂肪祖细胞(WAP)自组织成球体,并显示出增强的活力、增殖和成脂分化能力。作为概念验证,该多孔海藻酸盐水凝胶平台用于制备用于WAP和结肠癌细胞共培养的核壳球体,WAP簇分布在癌细胞聚集体周围,以研究细胞间相互作用。据信,这种有效的方法为工程化多孔结构的海藻酸盐水凝胶提供了一个强大且通用的平台,用于细胞载体应用和疾病建模。