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生长因子及生长因子受体在人类腭裂相关组织中的表达

Expression of growth factors and growth factor receptors in human cleft-affected tissue.

作者信息

Krivicka Benita, Pilmane Mara, Akota Ilze

机构信息

Institute of Anatomy and Anthropology of Riga Stradins University, Dzirciema street 16, Riga, LV-1007, Latvia.

出版信息

Stomatologija. 2013;15(4):111-8.

Abstract

OBJECTIVE. To investigate cleft disordered tissue in children with cleft palate and cleft lip with or without alveolar clefting for detection of local tissue growth factors and growth factor receptors and compare findings. Design. Morphological analysis of human tissue. Patients. Three groups were studied: 14 patients with cleft palate at the age from eight months to 18 years and two months, 12 patients with cleft lip with or without alveolar clefting in the age from four months to 15 years and four months and 11 control patients. RESULTS. In general, cleft palate disordered tissue showed more prominent expression of BMP2/4 (z=3.574; p=0.0004) and TGFβ (z=2.127; p=0.033), while expression of TGFBR3 significantly higher was only in connective tissue (z=3.822; p=0.0001). Cleft lip affected tissue showed significantly pronounced expression of FGFR1 in general as well as separately in epithelium. CONCLUSIONS. The marked and statistically significant expression of BMP 2/4 in cleft palate disordered soft tissue probably is delayed, but still proliferation and differentiation as well as tissue, especially, bone remodeling contributing signal. Cleft palate affected tissue show more prominent expression of TGFβ, still the weak regional expression of TGFβ type III receptors prove the disordered tissue growth and changed TGFβ signalling pathway in postnatal pathogenesis. In general, expression of TGFβ, BMP 2/4 and FGFR1 is significantly different, giving evidence to the involvement of these mentioned factors in the cleft severity morphopathogenesis.

摘要

目的。研究患有唇腭裂(伴或不伴牙槽裂)的儿童的腭裂紊乱组织,以检测局部组织生长因子和生长因子受体,并比较研究结果。设计。人体组织的形态学分析。患者。研究了三组:14例年龄在8个月至18岁零2个月的腭裂患者,12例年龄在4个月至15岁零4个月的唇裂(伴或不伴牙槽裂)患者,以及11例对照患者。结果。总体而言,腭裂紊乱组织中骨形态发生蛋白2/4(BMP2/4)(z = 3.574;p = 0.0004)和转化生长因子β(TGFβ)(z = 2.127;p = 0.033)的表达更为显著,而转化生长因子β受体3(TGFBR3)仅在结缔组织中的表达显著更高(z = 3.822;p = 0.0001)。唇裂受累组织总体上以及在上皮组织中分别显示出成纤维细胞生长因子受体1(FGFR1)的显著表达。结论。腭裂紊乱软组织中BMP 2/4的显著且具有统计学意义的表达可能延迟,但仍是增殖、分化以及组织(尤其是骨重塑)的促成信号。腭裂受累组织显示出TGFβ的更显著表达,然而TGFβ III型受体的弱区域表达证明了出生后发病机制中组织生长紊乱和TGFβ信号通路改变。总体而言,TGFβ、BMP 2/4和FGFR1的表达存在显著差异,证明这些上述因子参与了腭裂严重程度的形态发病机制。

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