GEP, a local growth factor, is critical for odontogenesis and amelogenesis

Granulin epithelin precursor (GEP) is a new growth factor that functions in brain development, chondrogenesis, tissue regeneration, tumorigenesis, and inflammation. The goal of this study was to study whether GEP was critical for odontogenesis and amelogenesis both in vivo and in vitro. The in situ hybridization and immunohistochemistry data showed that GEP was expressed in both odontoblast and ameloblast cells postnatally. Knockdown of GEP by crossing U6-ploxPneo-GEP and Sox2-Cre transgenic mice led to a reduction of dentin thickness, an increase in predentin thickness, and a reduction in mineral content in enamel. The in vitro application of recombinant GEP up-regulated molecular markers important for odontogenesis (DMP1, DSPP, and ALP) and amelogenesis (ameloblastin, amelogenin and enamelin). In conclusion, both the in vivo and the in vivo data support an important role of GEP in tooth formation during postnatal development.     

The role of invasive trophoblast in implantation and placentation of primates

We here review the evolution of invasive placentation in primates towards the deep penetration of the endometrium and its arteries in hominoids. The strepsirrhine primates (lemurs and lorises) have non-invasive, epitheliochorial placentation, although this is thought to be derived from a more invasive type. In haplorhine primates, there is differentiation of trophoblast at the blastocyst stage into syncytial and cellular trophoblast. Implantation involves syncytiotrophoblast that first removes the uterine epithelium then consolidates at the basal lamina before continuing into the stroma. In later stages of pregnancy, especially in Old World monkeys and apes, cytotrophoblast plays a greater role in the invasive process. Columns of trophoblast cells advance to the base of the implantation site where they spread out to form a cytotrophoblastic shell. In addition, cytotrophoblasts advance into the lumen of the spiral arteries. They are responsible for remodelling these vessels to form wide, low-resistance conduits. In human and great apes, there is additional invasion of the endometrium and its vessels by trophoblasts originating from the base of the anchoring villi. Deep trophoblast invasion that extends remodelling of the spiral arteries to segments in the inner myometrium evolved in the common ancestor of gorilla, chimp and human.     

Runx2条件性敲除小鼠釉质缺陷的部分挽救

该研究旨在探讨外源性Runx2过表达对小鼠成釉细胞Runx2敲除导致的釉质缺陷的挽救作用。采用免疫组化验证Runx2在Runx2条件性敲除且人源性Runx2过表达小鼠成釉细胞中的表达。HE染色观察成熟期成釉细胞形态及釉质基质蛋白残余。用体视显微镜和扫描电镜观察小鼠牙齿表面形态和釉柱结构。结果显示,RUNX2蛋白在出生后10天龄Tg;cKO小鼠成熟早期成釉细胞中成功表达。15天龄Tg;cKO小鼠与cKO小鼠相比,成熟晚期成釉细胞形态及排列未见明显改善,但釉质基质蛋白残余量明显减少。3月龄Tg;cKO小鼠与cKO小鼠相比,釉质磨耗减轻,釉柱间孔隙减少,釉柱排列更规则。该研究结果表明,人源性Runx2过表达可部分挽救小鼠成釉细胞Runx2敲除导致的釉质缺陷。     

An encyclopaedia of sexuality

Primate Sexuality. Comparative Studies of the Prosimians, Monkeys, Apes and Human Beings by Alan F. Dixson, Oxford University Press, 1998. £75.00 hbk, £32.50 pbk (656 pages) ISBN 0 19 850183 8/0 19 850182 X     

Copulatory patterns of primates as viewed in broad mammalian perspective

The goals of this review are to classify the patterns of copulatory behavior displayed by various species of primates, to compare them to the patterns of nonprimate mammalian species, and to search for correlates of the various patterns. Copulatory patterns are classified in relation to the presence or absence of four defining attributes: a lock, thrusting during intromissions, multiple intromissions, and multiple ejaculations. Literature on copulation in 67 primate species is reviewed, and a tentative classification is proposed for 33 primate species. Although neither social organization nor genital morphology provides a fully satisfactory relationship, there are indications that variations in copulatory behavior are related to variations in genital morphology.     

A study in situ of the effect of metallo- and serine proteinase inhibitors on the birefringence of the secretory stage enamel organic extracellular matrix

Abstract

Dental enamel formation occurs extracellularly and establishment of an ordered enamel organic extracellular matrix (ECM) seems to be crucial for proper construction of the enamel mineral phase. Polarizing microscopy shows that the ordered supramolecular structure of the secretory stage enamel organic ECM exhibits strong birefringence. We reported earlier that this birefringence is lost in unfixed specimens, probably due to extensive proteolytic cleavage of enamel proteins. Therefore, we investigated the association between enamel proteinase activities by analyzing the effects of metallo- and serine proteinase inhibitors in situ on the birefringence of the secretory stage enamel organic ECM. Male rats were used in the present study. After sacrifice, distal 10 mm fragments of upper incisors were removed and immersed for 15 h under continuous shaking at 37°C in one of the following solutions: 1) 10 mM Tris, pH 8.0; 150 mM NaCl (negative control, n = 8); 2) 2% paraformaldehyde and 0.5% glutaraldehyde in 0.2 M phosphate-buffered saline (PBS), pH 7.2 (positive control, n = 5); 3) 10 mM Tris, pH 8.0; 150 mM NaCl; 2 mM 1,10-phenanthroline (n = 9); 4) 10 mM Tris, pH 8.0; 150 mM NaCl; 2 mM phenylmethyl-sulfonyl fluoride (PMSF) (n = 8); 5) 10 mM Tris, pH 8.0; 150 mM NaCl; 2 mM 1,10-phenanthroline; 2 mM PMSF (n = 9). Samples then were immersed in fixative solution for 24 h and processed to obtain 5 μm thick longitudinal sections of the secretory stage enamel organic ECM. The sections were immersed in 80% glycerin for 30 min and analyzed by transmitted polarizing light microscopy. 1,10-Phenanthroline (inhibitor of metalloproteinases) and 1,10-phenanthroline + PMSF (inhibitor of serine proteinases) clearly prevented a decrease in the optical retardation of birefringence brightness from the tissue. PMSF alone promoted a slight preservation of the birefringence exhibited by the secretory stage enamel organic ECM. Rapid loss of birefringence in secretory stage enamel organic ECM that is not fixed immediately is caused by enamel proteinases and the activity of metalloproteinases seems to lead to preliminary degradation of the enamel organic ECM, which in turn facilitates subsequent serine proteinase activity.     

不同年龄组修复性牙本质生成情况探讨

目的观察不同年龄段人的牙齿在受到龋损刺激后,修复性牙本质的生成情况。方法收集5组不同年龄组含有牙本质浅层龋的离体牙,每组各5颗牙齿。制作标本切片,HE染色,显微镜下观察。测量修复性牙本质厚度,作统计学检验。结果5组不同年龄牙齿的修复性牙本质平均厚度分别为:3.36、2.6、2.8、4.2、3.36,统计学检验无明显差异。结论受龋损刺激后,不同年龄牙齿的修复性牙本质生成情况无明显差异。     

Odontoblast physiology

Odontoblasts are post-mitotic cells organized as a layer of palisade cells along the interface between the dental pulp and dentin. They are responsible for the formation of the physiological primary and secondary dentins. They synthesize the organic matrix of type I collagen and actively participate to its mineralization by secreting proteoglycans and non-collagenous proteins that are implicated in the nucleation and the control of the growth of the mineral phase. They also participate to the maintenance of this hard tissue throughout the life of the tooth by synthesizing reactionary dentin in response to pathological conditions (caries, attrition, erosion…).     

察干鼠、始壮鼠门齿釉质结构的立体分析

应用扫描电镜,观察阿尔泰察干鼠、始壮鼠门齿不同切面的釉质结构特征,通过分析得到下列结果。1．同一门齿的不同部位,其釉质形态虽有不同的表现形式,但反映釉质结构模式的两个主要特征不变,如HSB宽度和内外釉质层厚度比稳定．因此应用这些特征时,可以在不定位取样条件下比较．2．同一门齿的不同部位,内层HSB的倾斜度以及外层中放射状釉柱的倾斜度均有变化,变化范围可达0°—20°,但是,在通过门齿中心的各不同纵切面上,上述两个特征是稳定的,因此应用这些特征时,取样的定位范围要明确通过门齿的中心．3同一门齿的不同部位,其釉质层厚度、釉柱截面直径大小、釉柱形态等有变化,有时随外形的变化很大,因此应用这些特征时须要定位比较．4阿尔泰察干鼠为典型的多系结构,始壮鼠为典型的单系结构。