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通过投影立体光刻技术快速制造水凝胶微图案,用于研究自组织发育模式。

Rapid fabrication of hydrogel micropatterns by projection stereolithography for studying self-organized developmental patterning.

机构信息

Department of Bioengineering, Rice University, Houston, Texas, United States of America.

Department of Biosciences, Rice University, Houston, Texas, United States of America.

出版信息

PLoS One. 2021 Jun 2;16(6):e0245634. doi: 10.1371/journal.pone.0245634. eCollection 2021.

Abstract

Self-organized patterning of mammalian embryonic stem cells on micropatterned surfaces has previously been established as an in vitro platform for early mammalian developmental studies, complimentary to in vivo studies. Traditional micropatterning methods, such as micro-contact printing (μCP), involve relatively complicated fabrication procedures, which restricts widespread adoption by biologists. Here, we demonstrate a rapid method of micropatterning by printing hydrogel micro-features onto a glass-bottomed culture vessel. The micro-features are printed using a projection stereolithography bioprinter yielding hydrogel structures that geometrically restrict the attachment of cells or proteins. Compared to traditional and physical photomasks, a digitally tunable virtual photomask is used in the projector to generate blue light patterns that enable rapid iteration with minimal cost and effort. We show that a protocol that makes use of this method together with LN521 coating, an extracellular matrix coating, creates a surface suitable for human embryonic stem cell (hESC) attachment and growth with minimal non-specific adhesion. We further demonstrate that self-patterning of hESCs following previously published gastrulation and ectodermal induction protocols achieves results comparable with those obtained with commercially available plates.

摘要

哺乳动物胚胎干细胞在微图案化表面上的自组织模式已被确立为早期哺乳动物发育研究的体外平台,与体内研究相辅相成。传统的微图案化方法,如微接触印刷(μCP),涉及相对复杂的制造过程,这限制了生物学家的广泛采用。在这里,我们展示了一种通过将水凝胶微特征打印到玻璃底培养皿上来进行微图案化的快速方法。微特征使用投影立体光刻生物打印机进行打印,从而产生几何上限制细胞或蛋白质附着的水凝胶结构。与传统和物理光掩模相比,数字可调虚拟光掩模在投影仪中用于生成蓝光图案,从而以最小的成本和精力实现快速迭代。我们表明,利用这种方法和 LN521 涂层(一种细胞外基质涂层)的方案一起,可创建适合人类胚胎干细胞(hESC)附着和生长的表面,同时最小化非特异性附着。我们进一步证明,遵循先前发表的原肠胚形成和外胚层诱导方案的 hESC 自组织模式可实现与市售平板相当的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf9/8172057/99f282e5d633/pone.0245634.g001.jpg

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