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tich小鼠生长板内的细胞增殖。

Cell proliferation within the growth plate of the tich mouse.

作者信息

Ahmed Z, Archer J R, Brown R A

机构信息

Department of Plastic and Reconstructive Surgery, University College London Medical School, Rayne Institute, England.

出版信息

Bone. 1995 Apr;16(4 Suppl):305S-310S. doi: 10.1016/8756-3282(95)00025-9.

DOI:10.1016/8756-3282(95)00025-9
PMID:7626319
Abstract

The pattern of chondrocyte proliferation was studied in the proximal tibial growth plate of tich mice (gene symbol tch), a recessive mouse mutant, which is coisogenic with the A.TL strain. Specimens were qualitatively studied at time points of 2, 3, 4, 6, and 8 weeks of age by bromodeoxyuridine labeling of cell division and routine histology. At 2 weeks, when the lesion appeared as a full-width thickening of the growth plate, a greater proportion of cells appeared positively labeled in the proliferative zone. This concavity in the central portion of the growth plate became progressively more focal between 3 and 4 weeks to give a "tongue" of unresorbed, noncalcified cartilage in the central region of the tich growth plate. BrdUrd labeling indicated that the appearance of the cartilage tongue corresponded with increased cell division in the central region of the growth plate. At the same time, a "second" zone of cell division formed, within the zone of hypertrophy, such that labeled cells appeared to be set among chondrocytes with hypertrophic morphology. At stages after 4 weeks of age the focal feature disappeared as the growth plate returned to more normal morphology by maturity. It seems that this unique "second" zone of dividing cells may contribute to formation of an elongation of the nonresorbed tongue of cartilage. However, it is not likely to be the primary defect since growth plate changes were apparent at earlier stages.

摘要

在隐性小鼠突变体(基因符号tch)的胫骨近端生长板中研究了软骨细胞增殖模式,该突变体与A.TL品系同基因。通过细胞分裂的溴脱氧尿苷标记和常规组织学,在2、3、4、6和8周龄的时间点对标本进行定性研究。在2周龄时,当病变表现为生长板全宽增厚时,增殖区中出现阳性标记的细胞比例更高。在3至4周龄之间,生长板中央部分的这种凹陷逐渐变得更加局限,从而在tich生长板的中央区域形成一个未吸收、未钙化软骨的“舌状”结构。BrdUrd标记表明,软骨舌的出现与生长板中央区域细胞分裂增加相对应。与此同时,在肥大区内形成了一个“第二”细胞分裂区,使得标记细胞似乎分布在具有肥大形态的软骨细胞之间。在4周龄后的阶段,随着生长板在成熟时恢复到更正常的形态,局灶性特征消失。似乎这个独特的分裂细胞“第二”区可能有助于形成未吸收软骨舌的延长。然而,它不太可能是主要缺陷,因为生长板的变化在更早阶段就很明显。

相似文献

1
Cell proliferation within the growth plate of the tich mouse.tich小鼠生长板内的细胞增殖。
Bone. 1995 Apr;16(4 Suppl):305S-310S. doi: 10.1016/8756-3282(95)00025-9.
2
Cartilage calcification and limb bud growth in the developing tich mouse embryo.发育中的tich小鼠胚胎中的软骨钙化和肢芽生长。
Calcif Tissue Int. 1997 Jun;60(6):561-6. doi: 10.1007/s002239900280.
3
Growth plate abnormalities in a new dwarf mouse model: tich.一种新型侏儒小鼠模型——tich中的生长板异常
Bone Miner. 1994 Mar;24(3):235-44. doi: 10.1016/s0169-6009(08)80140-7.
4
Kinetic studies on epiphyseal growth cartilage in the normal mouse.
Bone. 1998 Apr;22(4):331-9. doi: 10.1016/s8756-3282(97)00286-x.
5
Cell cycle analysis of proliferative zone chondrocytes in growth plates elongating at different rates.不同生长速率下生长板中增殖区软骨细胞的细胞周期分析。
J Orthop Res. 1996 Jul;14(4):562-72. doi: 10.1002/jor.1100140410.
6
BMP-5 deficiency alters chondrocytic activity in the mouse proximal tibial growth plate.骨形态发生蛋白-5(BMP-5)缺乏会改变小鼠胫骨近端生长板中的软骨细胞活性。
Bone. 1999 Mar;24(3):211-6. doi: 10.1016/s8756-3282(98)00171-9.
7
Determination of proliferative characteristics of growth plate chondrocytes by labeling with bromodeoxyuridine.通过溴脱氧尿苷标记法测定生长板软骨细胞的增殖特性
Calcif Tissue Int. 1993 Feb;52(2):110-9. doi: 10.1007/BF00308319.
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Cell proliferation within the growth plate of long bones assessed by bromodeoxyuridine uptake and its relationship to glucose 6-phosphate dehydrogenase activity.
Bone Miner. 1990 Aug;10(2):121-30. doi: 10.1016/0169-6009(90)90087-v.
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Proliferation of the hypertrophic chondrocytes of the growth plate after physeal distraction. An experimental study in rabbits.骨骺牵张后生长板肥大软骨细胞的增殖。一项在兔子身上的实验研究。
Clin Orthop Relat Res. 1993 Dec(297):7-11.
10
End labeling studies of fragmented DNA in the avian growth plate: evidence of apoptosis in terminally differentiated chondrocytes.鸟类生长板中片段化DNA的末端标记研究:终末分化软骨细胞凋亡的证据
J Bone Miner Res. 1995 Dec;10(12):1960-8. doi: 10.1002/jbmr.5650101216.

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