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  • A day-55 iLung organoids presented airway-like and bronchi-like structure, alveoli-like structures. Scale bar = 500 μm.
  • Immunofluorescence staining of a day-60 iLung demonstrated the presence of both proximal airway and distal alveolar cell types, including ciliated cells (AcTUB), basal cells (NGFR), club cells (CC), goblet cell (MUC1), neuroendocrine cells (CHGA), type I cells (PDPN), type II cells (SP-B, SP-C), resident macrophages (CD68) and fibroblasts (VIM). Scale bar = 200 μm.
  • An iLung treated with 30-d bleomycin manifested increased dead cells, reduced bronchi/alveoli space, and collapsed architecture. Scale bar= 200 μm. Compared with control that treated with PBS only, 30-d bleomycin induction resulted in significant ECM accumulation in iLung, identified by the increased staining area of Collagen I and Fibronectin with immunofluorescence. Scale bar = 200 μm.

即用型 iPSC 肺类器官,3d0110

  • 使用 “人多能干细胞向肺类器官分化系统 (Ca. 3d0010) ” 诱导分化产生

  • 呈现出多级分叉结构与早期肺泡样结构,其中至少包含了肺泡 I-II 型细胞、基底细胞、棒状细胞、 纤毛细胞、肺神经内分泌细胞、巨噬细胞、间充质细胞、成纤维细胞等肺泡及气道生理相关的谱系类型

  • 经过肺纤维化、病毒感染、细菌感染等验证

  • 该研究肺脏发育、呼吸疾病及药物筛选的精准人源工具


产品规格

  • 12个 iLungs
  • 24个 iLungs
  • 48个 iLungs
  • 96个 iLungs
  • 定制 iLung

简介

“ 即用型 iPSC 源肺类器官 ” 呈现出多级分叉结构与早期肺泡样结构,其中至少包含了肺泡 I-II 型细胞、基底细胞、棒状细胞、 纤毛细胞、肺神经内分泌细胞、巨噬细胞、间充质细胞、成纤维细胞等肺泡及气道生理相关的谱系类型。支持肺脏发育机制的探索、呼吸道疾病的模拟与病理解析、药物开发、以及体内定植等研究。

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遗传信息






 • 类器官类型:• 来源:   • 性别:

   肺类器官  成纤维细胞  男

• 捐助者状态: • 年龄:

   健康  32

性能数据

Characteristics

即用型iPSC肺类器官, 3d0110(图1)


A day-55 iLung organoids presented airway-like and bronchi-like structure,  alveoli-like structures. Scale bar = 500 μm.




Characteristics


即用型iPSC肺类器官, 3d0110(图2)


Immunofluorescence staining of a day-60 iLung demonstrated the presence of both proximal airway and distal alveolar cell types, including ciliated cells (AcTUB+), basal cells (NGFR+), club cells (CC+), goblet cell (MUC1+), neuroendocrine cells (CHGA+), type I cells (PDPN+), type II cells (SP-B+, SP-C+), resident macrophages (CD68+) and fibroblasts (VIM+). Scale bar = 200 μm.




Application of iLung organoids

即用型iPSC肺类器官, 3d0110(图3)


An iLung treated with 30-d bleomycin manifested increased dead cells, reduced bronchi/alveoli space, and collapsed architecture. Scale bar = 200 μm.

Compared with control that treated with PBS only, 30-d bleomycin induction resulted in significant ECM accumulation in iLung, identified by the increased staining area of Collagen I and Fibronectin with immunofluorescence. Scale bar = 200 μm.

参考文献

  • Liu W, Zhao Y, Fan J, et al. Smoke and Spike: Benzo [a] pyrene Enhances SARS‐CoV‐2 Infection by Boosting NR4A2‐Induced ACE2 and TMPRSS2 Expression[J]. Advanced Science, 2023, 10(26): 2300834.

  • Hein R F C, Conchola A S, Fine A S, et al. Stable iPSC-derived NKX2-1+ lung bud tip progenitor organoids give rise to airway and alveolar cell types[J]. Development, 2022, 149(20): dev200693.

  • Han Y, Duan X, Yang L, et al. Identification of SARS-CoV-2 inhibitors using lung and colonic organoids[J]. Nature, 2021, 589(7841): 270-275.

  • Strikoudis A, Cieślak A, Loffredo L, et al. Modeling of fibrotic lung disease using 3D organoids derived from human pluripotent stem cells[J]. Cell reports, 2019, 27(12): 3709-3723. e5.

  • Porotto M, Ferren M, Chen Y W, et al. Authentic modeling of human respiratory virus infection in human pluripotent stem cell-derived lung organoids[J]. MBio, 2019, 10(3): 10.1128/mbio. 00723-19.

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