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软骨内成骨过程中骺板肥大软骨细胞“命运”的新形态学证据。

New morphological evidence of the 'fate' of growth plate hypertrophic chondrocytes in the general context of endochondral ossification.

机构信息

DSMC, University of Brescia, Brescia, Italy.

DMC University of Insubria, Varese, Italy.

出版信息

J Anat. 2020 Feb;236(2):305-316. doi: 10.1111/joa.13100. Epub 2019 Dec 9.

Abstract

The 'fate' of growth plate hypertrophic chondrocytes has been long debated with two opposing theories: cell apoptosis or survival with transformation into osteogenic cells. This study was carried out on the proximal tibial growth plate of rabbits using light microscopy, scanning and transmission electron microscopy. We focused particularly on the orientation of the specimens included in order to define the mineral deposition and the vascular invasion lines and obtain histological and ultrastructural images at the corresponding height of the plate. Chondrocyte morphology transformation through the maturation process (characterized by vesicles and then large cytoplasmic lacunae before condensation, fragmentation and disappearance of the nuclear chromatin) did not correspond to that observed in the 'in vitro' apoptosis models. These findings rather suggested the passage of free water from the cartilage matrix into a still live cell (swelling). The level of these changes suggested a close relationship with the mineral deposition line. Furthermore, the study provided evidence that the metaphyseal capillaries could advance inside the columns of stacked hypertrophic chondrocytes (delimited by the intercolumnar septa) without the need for calcified matrix resorption because the thin transverse septa between the stacked chondrocyte (below the mineral deposition line) were not calcified. The zonal distribution of cell types (hypertrophic chondrocytes, osteoblasts, osteoclasts and macrophages) did not reveal osteoclasts or chondroclasts at this level. Morphological and morphometric analysis recorded globular masses of an amorphous, necrotic material in a zone 0-70 μm below the vascular invasion line occasionally surrounded by a membrane (indicated as 'hypertrophic chondrocyte ghosts'). These masses and the same material not bound by a membrane were surrounded by a large number of macrophages and other blood cell precursors, suggesting this could be the cause of macrophage recall and activation. The most recent hypotheses based on genetic and lineage tracing studies stating that hypertrophic chondrocytes can survive and transform into osteoblasts and osteocytes (trans-differentiation) were not confirmed by the ultrastructural morphology or by the zonal comparative counting and distribution of cell types below the vascular invasion line.

摘要

骺板肥大软骨细胞的“命运”一直存在两种对立的理论:细胞凋亡或存活并转化为成骨细胞。本研究采用光镜、扫描电镜和透射电镜对兔胫骨近端骺板进行了研究。我们特别关注标本的取向,以便确定矿化沉积和血管侵入线,并在板的相应高度获得组织学和超微结构图像。通过成熟过程(以小泡为特征,然后是大细胞质腔,然后核染色质浓缩、碎裂和消失),软骨细胞形态的转变与“体外”凋亡模型中观察到的形态转变不一致。这些发现更表明自由水从软骨基质进入仍然存活的细胞(肿胀)。这些变化的程度表明与矿化沉积线密切相关。此外,该研究还提供了证据表明,骺板毛细血管可以在堆积的肥大软骨细胞柱内推进(由柱间间隔限定),而不需要矿化基质吸收,因为堆积软骨细胞之间的薄横向间隔(低于矿化沉积线)未矿化。细胞类型(肥大软骨细胞、成骨细胞、破骨细胞和巨噬细胞)的分区分布在该水平未显示破骨细胞或软骨母细胞。形态和形态计量分析记录了在血管侵入线以下 0-70μm 范围内的无定形、坏死物质的球形团块,偶尔被膜包围(表示为“肥大软骨细胞幽灵”)。这些团块和未被膜结合的相同物质被大量巨噬细胞和其他血细胞前体包围,表明这可能是巨噬细胞召回和激活的原因。基于遗传和谱系追踪研究的最新假说表明,肥大软骨细胞可以存活并转化为成骨细胞和成骨细胞(转分化),但超微结构形态或血管侵入线以下细胞类型的分区比较计数和分布并未证实这一假说。

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本文引用的文献

2
Fate of growth plate hypertrophic chondrocytes: death or lineage extension?
Dev Growth Differ. 2015 Feb;57(2):179-92. doi: 10.1111/dgd.12203. Epub 2015 Feb 24.
3
Chondrocytes transdifferentiate into osteoblasts in endochondral bone during development, postnatal growth and fracture healing in mice.
PLoS Genet. 2014 Dec 4;10(12):e1004820. doi: 10.1371/journal.pgen.1004820. eCollection 2014 Dec.
4
Hypertrophic chondrocytes can become osteoblasts and osteocytes in endochondral bone formation.
Proc Natl Acad Sci U S A. 2014 Aug 19;111(33):12097-102. doi: 10.1073/pnas.1302703111. Epub 2014 Aug 4.
6
NIH Image to ImageJ: 25 years of image analysis.
Nat Methods. 2012 Jul;9(7):671-5. doi: 10.1038/nmeth.2089.
7
C2C12 myoblast sensitivity to different apoptotic chemical triggers.
Micron. 2010 Dec;41(8):966-73. doi: 10.1016/j.micron.2010.07.002. Epub 2010 Jul 17.
9
Apoptotic DNA fragmentation can be revealed in situ: an ultrastructural approach.
Microsc Res Tech. 2009 Dec;72(12):913-23. doi: 10.1002/jemt.20735.
10
Integrin and cytoskeleton behaviour in human neuroblastoma cells during hyperthermia-related apoptosis.
Apoptosis. 2004 Sep;9(5):635-48. doi: 10.1023/B:APPT.0000038043.03799.6f.

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