Department of Materials Science and Engineering, University of Delaware, 210 South College Avenue, Newark, Delaware 19716, United States.
Department of Otolaryngology-Head & Neck Surgery, Thomas Jefferson University, 1020 Walnut Street, Philadelphia, Pennsylvania 19107, United States.
ACS Biomater Sci Eng. 2021 Dec 13;7(12):5749-5761. doi: 10.1021/acsbiomaterials.1c00745. Epub 2021 Nov 15.
engineering of salivary glands relies on the availability of synthetic matrices presenting essential cell-instructive signals to guide tissue growth. Here, we describe a biomimetic, hyaluronic acid (HA)-based hydrogel platform containing covalently immobilized bioactive peptides derived from perlecan domain IV (TWSKV), laminin-111 (YIGSR, IKVAV), and fibronectin (RGDSP). The HA network was established by the thiol/acrylate reaction, and bioactive peptides were conjugated to the network with high efficiency without significantly altering the mechanical property of the matrix. When encapsulated as single cells in peptide-modified HA hydrogels, human salivary gland stem/progenitor cells (hS/PCs) spontaneously organized into multicellular spheroids with close cell-cell contacts. Conjugation of RGDSP and TWSKV signals in HA gels significantly accelerated cell proliferation, with the largest spheroids observed in RGDSP-tagged gels. Peptide conjugation did not significantly alter the expression of acinar (), ductal (), and progenitor () markers at the mRNA level. Characterization of three-dimensional (3D) cultures by immunocytochemistry showed positive staining for keratin-5 (K5), keratin-14 (K14), integrin-β1, and α-amylase under all culture conditions, confirming the maintenance of the secretory progenitor cell population. Two-dimensional (2D) adhesion studies revealed that integrin-β1 played a key role in facilitating cell-matrix interaction in gels with RGDSP, IKVAV, and TWSKV signals. Overall, conjugation of the RGDSP peptide to HA gels improved cell viability, accelerated the formation of epithelial spheroids, and promoted the expansion of the progenitor cell population in 3D. This work represents an essential first step toward the development of an engineered salivary gland.
唾液腺的工程依赖于具有指导组织生长的必需细胞指令信号的合成基质的可用性。在这里,我们描述了一种仿生的、基于透明质酸(HA)的水凝胶平台,其中包含共价固定的源自 Perlecan 结构域 IV(TWSKV)、层粘连蛋白-111(YIGSR、IKVAV)和纤连蛋白(RGDSP)的生物活性肽。HA 网络通过巯基/丙烯酰胺反应建立,生物活性肽与网络高效结合,而不会显著改变基质的机械性能。当作为单细胞包封在肽修饰的 HA 水凝胶中时,人唾液腺干/祖细胞(hS/PCs)自发地形成具有紧密细胞间接触的多细胞球体。在 HA 凝胶中缀合 RGDSP 和 TWSKV 信号显著加速了细胞增殖,在 RGDSP 标记的凝胶中观察到最大的球体。肽缀合在 mRNA 水平上没有显著改变腺泡()、导管()和祖细胞()标志物的表达。通过免疫细胞化学对三维(3D)培养物进行的表征显示,在所有培养条件下,角蛋白-5(K5)、角蛋白-14(K14)、整合素-β1 和α-淀粉酶的染色均为阳性,证实了分泌祖细胞群体的维持。二维(2D)粘附研究表明,整合素-β1 在具有 RGDSP、IKVAV 和 TWSKV 信号的凝胶中促进细胞-基质相互作用中发挥关键作用。总体而言,将 RGDSP 肽缀合到 HA 凝胶中提高了细胞活力,加速了上皮球体的形成,并促进了 3D 中祖细胞群体的扩增。这项工作是开发工程化唾液腺的重要的第一步。