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潜伏性转化生长因子β结合蛋白3缺陷小鼠中的类骨硬化表型

Osteopetrosis-like phenotype in latent TGF-beta binding protein 3 deficient mice.

作者信息

Dabovic B, Levasseur R, Zambuto L, Chen Y, Karsenty G, Rifkin D B

机构信息

Department of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.

出版信息

Bone. 2005 Jul;37(1):25-31. doi: 10.1016/j.bone.2005.02.021.


DOI:10.1016/j.bone.2005.02.021
PMID:15878314
Abstract

LTBPs are extracellular matrix proteins resembling fibrillins. LTBP-1, 3, and 4 covalently bind latent TGF-beta and modulate tissue levels of this potent cytokine through regulation of its secretion, localization, and/or activation. To address LTBP function in vivo, we generated Ltbp-3 null mice. Ltbp-3-/- animals developed craniofacial abnormalities due to early ossification of the skull base synchondroses and displayed reduced body size. In addition, histological examination of Ltbp-3-/- skeletons revealed an increase in bone mass. The osteoblast numbers and mineral apposition rates were decreased in Ltbp-3-/- mice, whereas the osteoclast numbers were similar in null and wild type mice. Histological examination revealed persistence of cartilage remnants in Ltbp-3-/- trabecular bone. Taken together, these results indicate that the Ltbp-3-/- high bone mass phenotype was due to a defect in bone resorption. We hypothesize that lack of Ltbp-3 results in decreased levels of TGF-beta in bone and cartilage, which leads to compromised osteoclast function and decreased bone turnover.

摘要

潜伏性TGF-β结合蛋白(LTBPs)是类似于原纤蛋白的细胞外基质蛋白。LTBP-1、3和4与潜伏性转化生长因子-β(TGF-β)共价结合,并通过调节其分泌、定位和/或激活来调节这种强效细胞因子的组织水平。为了研究LTBP在体内的功能,我们培育了Ltbp-3基因敲除小鼠。Ltbp-3基因敲除小鼠由于颅底软骨结合过早骨化而出现颅面异常,并且体型减小。此外,对Ltbp-3基因敲除小鼠骨骼的组织学检查显示骨量增加。Ltbp-3基因敲除小鼠的成骨细胞数量和矿物质沉积率降低,而破骨细胞数量在基因敲除小鼠和野生型小鼠中相似。组织学检查显示Ltbp-3基因敲除小鼠的小梁骨中存在软骨残余物。综上所述,这些结果表明Ltbp-3基因敲除小鼠的高骨量表型是由于骨吸收缺陷所致。我们推测,缺乏Ltbp-3会导致骨骼和软骨中TGF-β水平降低,从而导致破骨细胞功能受损和骨转换减少。

相似文献

[1]
Osteopetrosis-like phenotype in latent TGF-beta binding protein 3 deficient mice.

Bone. 2005-7

[2]
Disruption of LTBP-4 function reduces TGF-beta activation and enhances BMP-4 signaling in the lung.

J Cell Biol. 2004-10-11

[3]
Latent TGF-beta binding proteins (LTBPs)-1 and -3 coordinate proliferation and osteogenic differentiation of human mesenchymal stem cells.

Bone. 2008-10

[4]
Parathyroid hormone stimulation and PKA signaling of latent transforming growth factor-beta binding protein-1 (LTBP-1) mRNA expression in osteoblastic cells.

J Cell Biochem. 2005-8-1

[5]
Bone defects in latent TGF-beta binding protein (Ltbp)-3 null mice; a role for Ltbp in TGF-beta presentation.

J Endocrinol. 2002-10

[6]
Disruption of the gene encoding the latent transforming growth factor-beta binding protein 4 (LTBP-4) causes abnormal lung development, cardiomyopathy, and colorectal cancer.

Genes Dev. 2002-9-1

[7]
Severe developmental bone phenotype in ClC-7 deficient mice.

Dev Biol. 2010-6-22

[8]
Growth retardation as well as spleen and thymus involution in latent TGF-beta binding protein (Ltbp)-3 null mice.

J Cell Physiol. 2003-8

[9]
Sequential deposition of latent TGF-beta binding proteins (LTBPs) during formation of the extracellular matrix in human lung fibroblasts.

Exp Cell Res. 2005-11-1

[10]
Bone abnormalities in latent TGF-[beta] binding protein (Ltbp)-3-null mice indicate a role for Ltbp-3 in modulating TGF-[beta] bioavailability.

J Cell Biol. 2002-1-21

引用本文的文献

[1]
The roles and regulatory mechanisms of TGF-β and BMP signaling in bone and cartilage development, homeostasis and disease.

Cell Res. 2024-2

[2]
Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients.

Heliyon. 2023-12-14

[3]
Multi-organ phenotypes in mice lacking latent TGFβ binding protein 2 (LTBP2).

Dev Dyn. 2024-2

[4]
Genetic/Protein Association of Atopic Dermatitis and Tooth Agenesis.

Int J Mol Sci. 2023-3-17

[5]
Frameshift Variant in British Shorthair Cats with Complex Skeletal Dysplasia.

Genes (Basel). 2021-11-29

[6]
Novel LTBP3 mutations associated with thoracic aortic aneurysms and dissections.

Orphanet J Rare Dis. 2021-12-14

[7]
A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in .

Genes (Basel). 2021-9-12

[8]
LTBP4 in Health and Disease.

Genes (Basel). 2021-5-23

[9]
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.

Am J Hum Genet. 2021-6-3

[10]
Acromelic dysplasias: how rare musculoskeletal disorders reveal biological functions of extracellular matrix proteins.

Ann N Y Acad Sci. 2021-4

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