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软骨和骨形成过程中介软骨骨化中细胞和结构细节的液相 ASEM 成像:Keap1 缺陷性佝偻病。

Liquid-phase ASEM imaging of cellular and structural details in cartilage and bone formed during endochondral ossification: Keap1-deficient osteomalacia.

机构信息

Division of Dental Pharmacology, Department of Developmental and Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8588, Japan.

Health and Medical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 6, Higashi 1-1-1, Tsukuba, Ibaraki, 305-8566, Japan.

出版信息

Sci Rep. 2021 Mar 11;11(1):5722. doi: 10.1038/s41598-021-84202-z.

Abstract

Chondrogenesis and angiogenesis drive endochondral ossification. Using the atmospheric scanning electron microscopy (ASEM) without decalcification and dehydration, we directly imaged angiogenesis-driven ossification at different developmental stages shortly after aldehyde fixation, using aqueous radical scavenger glucose solution to preserve water-rich structures. An embryonic day 15.5 mouse femur was fixed and stained with phosphotungstic acid (PTA), and blood vessel penetration into the hypertrophic chondrocyte zone was visualised. We observed a novel envelope between the perichondrium and proliferating chondrocytes, which was lined with spindle-shaped cells that could be borderline chondrocytes. At postnatal day (P)1, trabecular and cortical bone mineralisation was imaged without staining. Additional PTA staining visualised surrounding soft tissues; filamentous connections between osteoblast-like cells and osteocytes in cortical bone were interpreted as the osteocytic lacunar-canalicular system. By P10, resorption pits had formed on the tibial trabecular bone surface. The applicability of ASEM for pathological analysis was addressed using knockout mice of Keap1, an oxidative-stress sensor. In Keap1 femurs, we observed impaired calcification and angiogenesis of epiphyseal cartilage, suggesting impaired bone development. Overall, the quick ASEM method we developed revealed mineralisation and new structures in wet bone tissue at EM resolution and can be used to study mineralisation-associated phenomena of any hydrated tissue.

摘要

软骨生成和血管生成驱动软骨内骨化。我们使用未经脱钙和脱水的大气扫描电子显微镜(ASEM),使用富含水的自由基清除剂葡萄糖溶液在醛固定后不久直接对血管生成驱动的骨化进行成像,以保存富含水的结构。我们固定并染色了胚胎第 15.5 天的小鼠股骨,并用磷钨酸(PTA)染色,观察血管穿透肥大软骨细胞区。我们观察到一个新的围绕软骨膜和增殖软骨细胞的包膜,其内衬着梭形细胞,这些细胞可能是边缘型软骨细胞。在出生后第 1 天(P1),我们对未染色的小梁和皮质骨进行了矿化成像。额外的 PTA 染色显示了周围的软组织;皮质骨中类成骨细胞和骨细胞之间的丝状连接被解释为骨细胞陷窝-管系统。在 P10,胫骨小梁骨表面形成了吸收窝。我们使用 Keap1 的基因敲除小鼠(一种氧化应激传感器)来解决 ASEM 用于病理分析的适用性。在 Keap1 的股骨中,我们观察到骺软骨的钙化和血管生成受损,表明骨发育受损。总的来说,我们开发的快速 ASEM 方法以 EM 分辨率揭示了湿骨组织中的矿化和新结构,可用于研究任何含水组织的矿化相关现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/096d/7952587/0b2a2092ad00/41598_2021_84202_Fig1_HTML.jpg

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