微尺度化学
下丘脑
垂体
互惠的
生物
串扰
内分泌学
神经科学
激素
语言学
物理
光学
数学教育
哲学
数学
作者
Se-Ra Park,Myung Geun Kook,Soo‐Rim Kim,Jin Woo Lee,Young Soo Yu,Chan Hum Park,Soyi Lim,Byung‐Chul Oh,YunJae Jung,In‐Sun Hong
出处
期刊:Biofabrication
[IOP Publishing]
日期:2024-01-26
卷期号:16 (2): 025011-025011
被引量:9
标识
DOI:10.1088/1758-5090/ad22f1
摘要
Abstract Conventional 2D or even recently developed 3D in vitro culture models for hypothalamus and pituitary gland cannot successfully recapitulate reciprocal neuroendocrine communications between these two pivotal neuroendocrine tissues known to play an essential role in controlling the body’s endocrine system, survival, and reproduction. In addition, most current vitro culture models for neuroendocrine tissues fail to properly reflect their complex multicellular structure. In this context, we developed a novel microscale chip platform, termed the ‘hypothalamic–pituitary (HP) axis-on-a-chip,’ which integrates various cellular components of the hypothalamus and pituitary gland with biomaterials such as collagen and hyaluronic acid. We used non-toxic blood coagulation factors (fibrinogen and thrombin) as natural cross-linking agents to increase the mechanical strength of biomaterials without showing residual toxicity to overcome drawbacks of conventional chemical cross-linking agents. Furthermore, we identified and verified SERPINB2 as a reliable neuroendocrine toxic marker, with its expression significantly increased in both hypothalamus and pituitary gland cells following exposure to various types of toxins. Next, we introduced SERPINB2-fluorescence reporter system into loaded hypothalamic cells and pituitary gland cells within each chamber of the HP axis on a chip, respectively. By incorporating this SERPINB2 detection system into the loaded hypothalamic and pituitary gland cells within our chip platform, Our HP axis-on-chip platform can better mimic reciprocal neuroendocrine crosstalk between the hypothalamus and the pituitary gland in the brain microenvironments with improved efficiency in evaluating neuroendocrine toxicities of certain drug candidates.
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