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人内耳囊骨细胞的活力和空间分布:基于向量体视学的定量研究。

The viability and spatial distribution of osteocytes in the human labyrinthine capsule: a quantitative study using vector-based stereology.

机构信息

Rigshospitalet, University of Copenhagen, Department of Otorhinolaryngology, Blegdamsvej 9, 2100 Copenhagen, Denmark.

出版信息

Hear Res. 2010 Dec 1;270(1-2):65-70. doi: 10.1016/j.heares.2010.09.007. Epub 2010 Sep 27.

Abstract

BACKGROUND

Bone remodeling is highly inhibited around the labyrinthine space, most likely by the action of the anti-resorptive cytokine osteoprotegerin (OPG). Inner ear OPG may enter the bony otic capsule through the lacuno-canalicular porosity (LCP). The aim of the study was to investigate the patency of this extracellular signaling pathway by exploring the viability, age dependency and spatial distribution of capsular osteocytes.

METHODS

Sixty-five bulk-stained undecalcified human temporal bones were selected to span the ages from 30th gestational week to 95 years. Osteocytes within 1000 μm wide iso-concentric perilabyrinthine zones of bone were identified by 3-D vector calculations and the number of cells per unit of bone volume estimated within each zone by optical dissectors.

RESULTS

From a high initial numerical density and a centripetal distribution of viable osteocytes, the density declined over time. This effect was higher towards the inner ear space and shifted viable osteocytes into to a centrifugal distribution with age. Contrary to this, non-viable osteocytes accumulated centripetally around the inner ear space and accounted for 50% of all lacunae at 80 years of age. Non-viable osteocytes were heterogeneously distributed forming islets of varying size surrounded by the intact and viable parts of the LCP.

CONCLUSION

The simultaneous presence of high numbers of non-viable osteocytes within a dense network of viable osteocytes is unique for the bony otic capsule. Viable osteocytes may sustain a life-long anti-resorptive signaling pathway for inner ear OPG. Clustering of non-viable osteocytes may locally impede the effect of OPG leaving the ghost regions unprotected against focal bone remodeling, as in human otosclerosis.

摘要

背景

骨重塑在迷路区域受到高度抑制,这很可能是抗吸收细胞因子骨保护素(OPG)的作用。内耳 OPG 可能通过腔隙管孔隙(LCP)进入骨性耳囊。本研究旨在通过探索囊状成骨细胞的活力、年龄依赖性和空间分布,来研究这种细胞外信号通路的通畅性。

方法

选择 65 个未经脱钙的整块染色的人颞骨,跨越从 30 孕周到 95 岁的年龄范围。通过 3-D 向量计算,在骨的 1000μm 宽等同心迷路区范围内识别成骨细胞,并通过光学切割器在每个区域内估计单位骨体积的细胞数。

结果

从初始高数量的有活力的成骨细胞和向心分布,密度随时间降低。这种效应在内耳空间方向更高,并随着年龄的增长将有活力的成骨细胞推向离心分布。与此相反,无活力的成骨细胞在内耳空间周围向心聚集,并在 80 岁时占所有腔隙的 50%。无活力的成骨细胞呈不均匀分布,形成大小不一的胰岛,周围是完整和有活力的 LCP 部分。

结论

在密集的有活力的成骨细胞网络中同时存在大量无活力的成骨细胞,这是骨性耳囊的独特特征。有活力的成骨细胞可能维持着对内耳 OPG 的抗吸收信号通路的终生作用。无活力的成骨细胞的聚集可能会局部阻碍 OPG 的作用,使鬼区不受局灶性骨重塑的保护,就像在人类耳硬化症中一样。

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