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ZOOLOGISCHER ANZEIGER · 2023 · IF 1.4

Location of olfactory organs and architecture of gustatory organs in the poultry red mite, Dermanyssus gallinae (Acari: Dermanyssidae)

Xiaoxiao Qi,Huan Li,Xin Liu,Bohan Wang,Jiali Meng,Qi Liu,Weiwei Sun,Baoliang Pan

Dermanyssus gallinae is a hematophagous ectoparasitic mite in the poultry industry worldwide. Its current control mainly relies on spraying acaricides with many deficiencies. It's urgently needed to develop novel control approaches, such as pheromones. The pheromones are detected by chemoreceptors , which are not well investigated in D. gallinae . In the current study, Y-tube olfactometer bioassays revealed that extracts of feces of mites could attract D. gallinae , indicating aggregation pheromones existed in feces. After varnishing the tips of the foreleg tarsi, the female mites' response to feces extracts disappeared in Y-tube olfactometer bioassays. Still, their response to guanine (a non-volatile compound acting as a potential arrestment pheromone) remained in filter paper contact bioassays. These results suggested that the sensilla at tips of the foreleg tarsi had olfactory function, and the sensilla at the tips of the pedipalpal tarsi could have gustatory function and the gustatory organs were located in other body parts of female mites. Through scanning electron microscopy (SEM), it was found that adults and nymphs possess a cluster of 8 peg-like sensilla as well as 2 blunt, peg-like sensilla at the tip of each pedipalpal tarsus. Nevertheless, the larvae had only a cluster of 5 blunt peg-type sensilla. Each sensillum has a terminal pore or depression, suggesting it functions as gustatory organ. The present study confirmed the location and explored the architecture of gustatory organs of D. gallinae , which would facilitate the development of novel control method based on pheromones .

CAS / MDL: 73-40-5
研究领域: 昆虫学 · 寄生虫学
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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A · 2025 ·Vol. 113 ·期 3 ·e37892 · IF 3.9

3D Bioprinting Inner Ear Organ of Corti Organoids Induce Hair Cell Regeneration

Yingjie Wang,Haobo Li,Junming Zhang,Mengyu Chen,Yiyin Pan,Xiangxin Lou

Hearing loss is often regarded as “invisible disability” which seriously affects the quality of life. The majority of hearing loss cases are caused by the damage to inner ear hair cells or connected spiral ganglion cells, and there is a lack of effective treatment measures. In recent years, significant progress has been made in the use of two-dimensional (2D) culture systems to induce the regeneration of auditory cells. However, the regenerated hair cells cannot form effective functional ciliary bundles under the 2D system, let alone establish synaptic contact with spiral ganglion cells, so they cannot truly achieve physiological repair of hearing. In this study, our aim is to construct a three-dimensional (3D) organ of Corti organoid through 3D bioprinting, which combines “3D culture scaffold + multiple induction signals + inner ear stem cells.” Then we evaluate the effects of the organoids on the differentiation of inner ear stem cells into auditory cells. We found that the organoids promoted adhesion and growth of inner ear stem cells, as well as the production of hair cells and nerve cells. The research may develop a novel approach for studying auditory cell regeneration and hearing loss repair.

CAS / MDL: 760-93-0
研究领域: 再生医学 · 听力科学 · 组织工程学
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BIOSENSORS & BIOELECTRONICS · 2025 · IF 10.5

Determining the Optimal Transplantation Window in Hepatic Organoids via Real-Time Biosensing of Vascularization and Metabolic Maturation Utilizing the Integrated Organoid-on-a-Chip Platform

Chenwei Sun,Guohua Wu,Di Wu,Lin Wu,Qingrui Lu,Wenqi Hu,Qijun Du,Jiashu Wang,Ao Xie,Mengjiao Xia,Haijie Hu,Bangchuan Hu,Jian Huang,Shuqi Wang

Hepatic organoid transplantation is hypothesized to achieve maximal therapeutic benefit when vascular integration coincides with peak metabolic function. However, conventional endpoint-based evaluation methods cannot dynamically track these processes in real time, limiting precise determination of the optimal transplantation window. To address this challenge, we developed a biosensor-integrated organoid-on-a-chip. This platform enables simultaneous, real-time monitoring of vascularization through nitric oxide (NO) and hepatic metabolic function through urea. Under controlled flow conditions, the biosensor-integrated organoid-on-a-chip revealed that flow-induced mechanostimulation synchronizes endothelial and hepatocyte maturation. The biosensors integrated chip further identified a critical day-5 inflection point, corresponding to maximal biomarker levels and defining the optimal transplantation window. Transplantation at this window restored approximately 93% of liver function and lobular architecture in cirrhotic mice, whereas grafts transplanted before or after this window showed 50–70% lower therapeutic efficacy. These findings validate the transplantation window hypothesis and provide a real-time, quantitative framework for quality control in organoid-based regenerative therapies.

研究领域: 再生医学 · 肝脏病学 · 生物医学工程 · 类器官技术 · 转化医学 · 代谢生物学 · 组织工程
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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY · 2018 · IF 3.974

Molybdenum and Cadmium exposure influences the concentration of trace elements in the digestive organs of Shaoxing duck (Anas platyrhyncha)

Zhiyue Liao,Huabin Cao,Xueyan Dai,Chenghong Xing,Xiongwei Xu,Gaohui Nie,Caiying Zhang

To investigate the toxic effects of Molybdenum (Mo) and Cadmium (Cd) on trace elements in digestive organs of Shaoxing duck ( Anas platyrhyncha ), 120 Shaoxing ducks were randomly divided into control group and 5 treatment groups which were treated with a commercial diet containing different dosages of Mo and Cd. On the 60th and 120th days, the beak, esophagus, glandular stomach, muscular stomach, small intestine, large intestine and feces were collected to determine contents of Mo, Cd, copper (Cu), iron (Fe), zinc (Zn) and selenium (Se), then correlation analysis was performed. The results showed that Cd content in digestive organs significantly increased in co-treated groups compared to single treated groups and Mo concentration increased in Mo-treated groups compared to control group, whereas Cu, Fe, Zn and Se concentrations in digestive organs decreased in co-treated groups. Furthermore, Cd and Mo were mainly accumulated in the small intestine and esophagus, respectively. There was a strongly positive correlation between Cd and Mo while they had negative correlation with Cu, Fe, Zn and Se, respectively. In feces, Mo and Fe contents in high dose of Mo group and high Mo combined with Cd group were significantly higher than those in control group, and Cu content in all treated groups significantly increased and Cd, Zn and Se concentrations had no difference. The results indicated that dietary Mo or/and Cd might disturb homeostasis of trace elements in digestive organs of Shaoxing duck. Moreover, the two elements presented a synergistic relationship.

研究领域: 动物生理学 · 环境毒理学 · 营养学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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ANALYTICA CHIMICA ACTA · 2021 · IF 6.558

Investigation on selenium and mercury interactions and the distribution patterns in mice organs with LA-ICP-MS imaging

Jinhui Liu,Jiasen Cui,Xing Wei,Weitao Li,Chunran Liu,Xuewen Li,Mingli Chen,Yu Fan,Jianhua Wang

It is the first time to investigate local distribution patterns of mercury (Hg) in mice organs after Hg and Se exposure with detection of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Two batch of adult mice were employed to be exposed to inorganic mercury (iHg) and methylmercury (MeHg) with or without Se at the dose of 55 μmol kg −1 . Tissue sections of brain, kidney, liver, and spleen from one batch mice were prepared to get local imaging of Hg by LA-ICP-MS. Tissues from another batch mice were used to quantify Hg and Se in tissues with ICP-MS after acid digestion . The results indicated that, for mice exposed to iHg, Hg mainly distributed in kidney, a little in liver, and hardly in brain and spleen; for mice exposed to MeHg, lower amount of Hg was found in kidney, liver and spleen, and almost no Hg was found in brain. It was interesting that for Hg and Se co-administration groups, higher level of Hg was observed in kidney, liver, spleen and even in brain than single Hg administration groups. In addition, Se level in organ tissues increased obviously not only in Se exposure group but also in MeHg exposure group, while the phenomenon was not observed in iHg exposure group. HepG2 cells were employed to investigate Se and Hg interactions in single cell level, similar bioaccumulation behavior of Hg was found between cells and mice organs. Higher level of Hg was observed in cells cultured with Se and Hg medium than cells cultured with single Hg medium. The results are expected to provide new insight to investigate Hg and Se interactions in animal bodies and in-vitro cells.

CAS / MDL: 22967-92-6
研究领域: 环境科学 · 毒理学 · 分析化学
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Polymers · 2021 ·Vol. 13 ·期 22 ·4028 · IF 4.329

The Effect of Agarose on 3D Bioprinting

Chi Gong,Zhiyuan Kong,Xiaohong Wang

In three-dimensional (3D) bioprinting, the accuracy, stability, and mechanical properties of the formed structure are very important to the overall composition and internal structure of the complex organ. In traditional 3D bioprinting, low-temperature gelatinization of gelatin is often used to construct complex tissues and organs. However, the hydrosol relies too much on the concentration of gelatin and has limited formation accuracy and stability. In this study, we take advantage of the physical crosslinking of agarose at 35–40 °C to replace the single pregelatinization effect of gelatin in 3D bioprinting, and printing composite gelatin/alginate/agarose hydrogels at two temperatures, i.e., 10 °C and 24 °C, respectively. After in-depth research, we find that the structures manufactured by the pregelatinization method of agarose are significantly more accurate, more stable, and harder than those pregelatined by gelatin. We believe that this research holds the potential to be widely used in the future organ manufacturing fields with high structural accuracy and stability.Keywords:3D bioprinting;agarose;pregelatinization;organ manufacturing

研究领域: 生物工程 · 再生医学
✓ 已验证 DOI PubMed 高影响因子
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IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-PLANT · 2020 ·Vol. 57 ·期 1 ·39-47 · IF 1.814

Organogenesis and high-frequency plant regeneration in Caryopteris terniflora Maxim. using thidiazuron

Wu Qinggui,Yang Honglin,Sun Yuxi,Hu Jinyao,Zou Lijuan

In vitro culture is employed as a means of producing plant materials from medicinal plants to meet the increasing demands of the market. Herein, we focused on an efficient protocol for organogenesis through two pathways in six explant types from Caryopteris terniflora Maxim ( C. terniflora ), a medicinal and ornamental plant. For direct organogenesis, the maximum number of shoots per internode explant (62.5) was achieved on Murashige and Skoog (MS) medium containing 3.0 mg L −1 thidiazuron (TDZ) and the maximum number of shoot tips per explant (45.5) was obtained by 1.5 mg L −1 TDZ, with 100% response. A protocol was also developed for indirect organogenesis from leaf, leaf-petiole, petiole, and root explants on MS basal medium containing a range of TDZ concentrations. Leaf-petiole explants induced more adventitious shoots (57.6 per explant) and leaves (31.4 per explant) than petioles (37.5 per explant) or roots (25.0 per explant), and the differentiation rate ranged from 87.2 to 100%. The regenerated shoots were elongated on MS medium containing 0.3 mg L −1 α-naphthaleneacetic acid (NAA) and 1.0 mg L −1 gibberellic acid (GA 3 ). The elongated shoots developed roots on ½ MS medium containing 0.3 mg L −1 NAA. Successful acclimatization of rooted plantlets in a greenhouse was achieved with 100% survival. Furthermore, the embryogenic-like structure was observed and the morphological characteristics of C. terniflora assessed at different stages of in vitro development. Our protocol offers, for the first time, an efficient, scalable propagation procedure for C. terniflora useful for large-scale cultivation for the purposes of conservation and genetic manipulation.

研究领域: 植物学 · 药用植物研究
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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-23 · IF 15.7

Divide-and-conquer strategy with engineered ossification center organoids for rapid bone healing through developmental cell recruitment

Zhang Xianzhu,Jiang Wei,Wu Xinyu,Xie Chang,Zhang Yi,Li Liying,Gu Yuqing,Hu Zihao,Zhai Xinrang,Liang Renjie,Zhang Tao,Sun Wei,Ye Jinchun,Wei Wei,Wang Xiaozhao,Hong Yi,Zhang Shufang,Cai Youzhi,Zou Xiaohui,Hu Yihe,Ouyang Hongwei

Current approaches for bone repair predominantly target localized delivery of growth factors that are aimed at the coupling of angiogenesis and osteogenesis. However, delayed revascularization and regeneration of critical-sized bone defects are still challenging. In this study, we engineer an ossification center-like organoid (OCO) that consist of an inner-core bone morphogenetic and neurotrophic spheroid generated via MSCs-loaded 3D printing, alongside the interstitially distributed outer-shell proangiogenic neurotrophic phase. Our results demonstrate that collective implantation of OCOs achieves rapid bone bridging with successive OC-like bone ossicles formation across the bone defect in a “divide-and-conquer” way. Single-cell RNA sequencing analysis unveils a developmentally mimicking stem cell community that dominated with Krt8 + skeletal stem cells (SSCs) is uniquely recruited by the pro-regenerative in-situ organoid fusion and maturation. Particularly noteworthy is the specific expansion of Krt8 + SSCs concomitant with the simultaneous reduction of Has1 + migratory fibroblasts (MFs) post-OCO implantation. Furthermore, cross-species comparisons employing machine learning reveal high resemblance of the relative Krt8 + SSCs/Has1 + MFs composition in bone regeneration with that in public data from developmental bone tissues. Our findings advocate an approach akin to “divide-and-conquer” utilizing engineered OC-like organoids for prompt regeneration of large-sized bone defects.

CAS / MDL: 7550-35-8
研究领域: 生物医学工程 · 再生医学 · 发育生物学 · 组织工程
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CURRENT MOLECULAR MEDICINE · 2025 ·Vol. 25 ·期 3 ·343-352 · IF 2.5

Study on the Mechanism of Notch Pathway Mediates the Role of Lenvatinib-resistant Hepatocellular Carcinoma Based on Organoids

Weiqing Feng,Haixiong Zhang,Qing Yu,Hao Yin,Xiaowei Ou,Jie Yuan,Liang Peng

Background The emergence of treatment resistance has hindered the efficacy of targeted therapies used to treat patients with hepatocellular carcinoma (HCC). Objective This study aimed to explore the mechanism of organoids constructed from lenvatinib-resistant HCC cells. Methods Hep3B cell and human HCC organoids were cultured and identified using hematoxylin and eosin staining and Immunohistochemistry. Lenvatinib-sensitive/ resistant Hep3B cells were constructed using lenvatinib (0, 0.1, 1, and 10 μM) and lenvatinib (0, 1, 10, and 100 μM). qRT-PCR and flow cytometry were utilized to deter-mine HCC stem cell markers CD44, CD90, and CD133 expressions. Transcriptome sequencing was performed on organoids. Western blot evaluated Notch pathway-related proteins (NOTCH1 and Jagged) expressions. Furthermore, DAPT, an inhibitor of the Notch pathway, was used to investigate the effects of lenvatinib on resistance or stemness in organoids and human HCC tissues. Results The organoids were successfully cultivated. With the increase of lenvatinib concentration, sensitive cell organoids were markedly degraded and ATP activity was gradually decreased, while there was no significant change in ATP activity of resistant cell organoids. CD44 expressions were elevated after lenvatinib treatment compared with the control group. KEGG showed that lenvatinib treatment of organoids constructed from Hep3B cells mainly activated the Notch pathway. Compared with the control group, NOTCH1 and Jagged expressions elevated, and ATP activity decreased after lenvatinib treatment. However, ATP activity was notably decreased after DAPT treatment. Moreover, DAPT inhibited lenvatinib resistance and the increase in the expressions of CD44 caused by lenvatinib. Besides, 100 μM lenvatinib significantly inhibited the growth and ATP activity of human HCC organoids, and DAPT increased the inhibitory effect of lenvatinib. Conclusion Lenvatinib regulated resistance and stemness in organoids via the Notch pathway.

CAS / MDL: 96949-21-2
研究领域: 肿瘤学 · 分子生物学 · 转化医学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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SCIENCE OF THE TOTAL ENVIRONMENT · 2025 · IF 8

Spatial metabolomics revealed multi-organ toxicity and visualize metabolite changes induced by borneol in zebrafish

Bin Li,Chenglong Sun,Yanan Yang,Chenqinyao Li,Te Zheng,Jiashuo Zhou,Yun Zhang

This study focuses on the potential hazards of borneol (BO) to aquatic organisms and human health. BO has antibacterial, anti-inflammatory and antioxidant activities, and is widely used in medicine, cosmetics, and detergents. In this study, zebrafish was used as a model organism to systematically evaluate the effects of BO on the heart, liver, kidney, and nervous system. The effects of BO on metabolites of zebrafish were studied using MALDI-MSI. The results showed that a high concentration of BO (500 μM) could induce morphological abnormalities (swim-bladder loss, spinal curvature, body-length shortening), cardiotoxicity (decreased heart rate, increased SV-BA distance), hepatotoxicity (reduced liver area index), and neurotoxicity (impaired behavioral ability, and dopamine neuron development deficits), but there was no renal toxicity observed in zebrafish. Additionally, MALDI-MSI analysis showed that BO exposure significantly altered the levels of metabolites, including phospholipids, fatty acids, choline, and amino acids. The contents of PC-34:1, PC-34:2, PI-36:4, PE-36:1, LysoPE-22:5, LysoPC-18:1, FA-18:2, phenylalanine, lysine and glutathione were significantly increased, while the contents of PC-38:6 and PC-40:6 were significantly decreased. Notably, BO elicited a significant alteration in the mRNA expression levels of genes associated with phospholipid metabolism, fatty acid metabolism, choline metabolism, and amino acid metabolism (such as elovl5 , chpt1 , chka , setd7 , hgd ). This study revealed that BO exerted toxicity on multiple organs and demonstrated that BO causes metabolic dysregulation in zebrafish. These findings provide a novel insight into the toxicity of BO.

CAS / MDL: 2243-62-1
研究领域: 毒理学 · 环境科学 · 代谢组学
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Bioengineering & Translational Medicine · 2022 ·Vol. 8 ·期 1 ·e10327 · IF 10.684

Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative

Zi-Yan Xu,Jin-Jian Huang,Ye Liu,Can-Wen Chen,Gui-Wen Qu,Ge-Fei Wang,Yun Zhao,Xiu-Wen Wu,Jian-An Ren

Organoids hold inestimable therapeutic potential in regenerative medicine and are increasingly serving as an in vitro research platform. Still, their expanding applications are critically restricted by the canonical culture matrix and system. Synthesis of a suitable bioink of bioactivity, biosecurity, tunable stiffness, and printability to replace conventional matrices and fabricate customized culture systems remains challenging. Here, we envisaged a novel bioink formulation based on decellularized extracellular matrix (dECM) from porcine small intestinal submucosa for organoids bioprinting, which provides intestinal stem cells (ISCs) with niche-specific ECM content and biomimetic microstructure. Intestinal organoids cultured in the fabricated bioink exhibited robust generation as well as a distinct differentiation pattern and transcriptomic signature. This bioink established a new co-culture system able to study interaction between epithelial homeostasis and submucosal cells and promote organoids maturation after transplantation into the mesentery of immune-deficient NODSCID-gamma (NSG) mice. In summary, the development of such photo-responsive bioink has the potential to replace tumor-derived Matrigel and facilitate the application of organoids in translational medicine and disease modeling.

CAS / MDL: 9004-61-9 85073-19-4
研究领域: 再生医学 · 组织工程 · 干细胞生物学 · 生物材料科学
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STAR Protocols · 2024 · IF 1.3

Protocol to encapsulate cerebral organoids with alginate hydrogel shell to induce volumetric compression

Zitian Wang,Xiaowei Tang,Davit Khutsishvili,Gan Sang,Edgar A. Galan,Jie Wang,Shaohua Ma

Summary In vitro organoids, including cerebral organoids, are usually developed without mechanical compression, which may contribute to a delay in maturation. Here, we present a protocol for encapsulating cerebral organoids with a thin shell of low-concentration alginate hydrogel. We describe steps for organoid generation, microfluidic chip culture, Matrigel coating, expansion culture, and alginate encapsulation. We then detail procedures for maturation culture and organoid characterization. The moderate compressive stimulation that the shell provides promotes cell proliferation and neuronal maturation. For complete details on the use and execution of this protocol, please refer to Tang et al. 1

CAS / MDL:
研究领域: 神经科学 · 组织工程 · 生物医学工程 · 细胞生物学
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