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胎儿及新生期骨硬化(op/op)小鼠造血功能的发育与建立

The development and establishment of hemopoiesis in fetal and newborn osteopetrotic (op/op) mice.

作者信息

Nilsson S K, Bertoncello I

机构信息

Cell Biology Group, Peter MacCallum Cancer Institute, Melbourne, Victoria, Australia.

出版信息

Dev Biol. 1994 Aug;164(2):456-62. doi: 10.1006/dbio.1994.1215.

Abstract

Previous studies of young CSF-1-less osteopetrotic (op/op) mice demonstrate a severe deficiency of both macrophages and osteoclasts, resulting in excessive bone formation, occlusion of the marrow cavity, and reduced hemopoietic activity. The accompanying splenomegaly and prolonged splenic hemopoiesis observed in these mice suggests that osteopetrosis may perturb the normal progression of fetal hemopoietic development and obstruct the seeding of hemopoietic precursors into the bone marrow. This study demonstrates that the absence of CSF-1 does not affect the progression of hemopoietic development in fetal op/op mice until after colonization of the bone marrow. Significant deficiencies in marrow cellularity and progenitor cell content in the long bones of op/op mice were not evident prior to Day 2 postnatal, suggesting that the altered hemopoietic state of young op/op mice is not a consequence of abnormal fetal hemopoietic development, but is primarily due to the lack of functional osteoclasts in op/op fetuses and hence, impaired remodeling of the marrow cavity after birth.

摘要

先前对缺乏集落刺激因子-1(CSF-1)的年轻骨石化(op/op)小鼠的研究表明,巨噬细胞和破骨细胞均严重缺乏,导致骨形成过多、骨髓腔闭塞以及造血活性降低。在这些小鼠中观察到的伴随脾肿大和脾脏造血延长表明,骨石化可能扰乱胎儿造血发育的正常进程,并阻碍造血前体细胞植入骨髓。本研究表明,在骨髓定植之前,CSF-1的缺失并不影响胎儿op/op小鼠的造血发育进程。op/op小鼠长骨中骨髓细胞数量和祖细胞含量的显著不足在出生后第2天之前并不明显,这表明年轻op/op小鼠造血状态的改变不是胎儿造血发育异常的结果,而是主要由于op/op胎儿中功能性破骨细胞的缺乏,因此出生后骨髓腔的重塑受损。

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