SD大鼠与巴马小型猪的皮肤组织学比较

目的研究及观察SD大鼠和巴马小型猪皮肤的正常比较组织学。方法取SD大鼠和巴马小型猪不同部位的皮肤进行石蜡切片、HE染色,光学显微镜观察。结果两种动物的皮肤组织学结构在以下方面存在着显著差异：1.SD大鼠的毛囊成簇分布,平均3～9成群,而巴马小型猪的毛囊较稀少;2.SD大鼠表皮较薄,没有透明层,基底细胞缺乏异质性,真皮与表皮连接面平坦,没有皮钉;而在巴马小型猪皮肤表皮和真皮连接区,有上下交错的表皮皮钉和真皮乳头;3.SD大鼠的真皮结构相对松散,真皮血管系统不发达,而巴马小型猪皮肤的真皮网织层和乳头层交界的地方,水平分布着很多的浅表小静脉和小动脉丛,这种血管分布的方式与人类皮肤中的血管分布极为类似;4.SD大鼠的汗腺只局限于足垫的皮肤,汗腺上皮只有一种细胞类型,腺细胞呈立方形或矮柱状,胞核圆形,导管短而弯曲,由两层上皮细胞组成。而巴马小型猪皮肤的汗腺是顶泌汗腺,分布于真皮和脂肪相接的真皮深层,分泌部为粗管,管腔大,盘曲成团。腺细胞呈立方形或扁平,胞核圆形或长梭形。腺细胞与基膜之间也有肌上皮细胞。导管较细而直,开口于毛囊上段。     

无毛小鼠不同年龄皮肤结构的比较研究

采用组织学方法对１月龄、２月龄、老龄豫医无毛小鼠皮肤结构进行了比较,结果发现,各年龄段表皮均有一层角化过度的角质层,毛干消失,毛球结构不正常,毛囊被一些角化物质充填。但真皮层差别很大。１月龄皮肤为肉色偏红,切片可见表皮层较厚,真皮内没有包囊;２月龄皮肤为肉色,表皮层较１月龄薄,毛囊腔大,真皮深层及皮下组织内有一些大小不等的包囊;老龄鼠皮肤为淡黄色,头部和体侧形成特别皱纹和褶痕,皮肤脆性大,易撕裂,表皮层薄,角化严重,真皮层被包囊扩张。包囊直径约为２月龄的４倍,内含一些角化物和脂肪样物质     

角蛋白15在大鼠皮肤发育中表达的研究

目的研究角蛋白15(K15)在大鼠皮肤发育中的表达状况,定位表皮干细胞.方法以不同年龄大鼠背部皮肤为标本,用组织学方法,观察出生后大鼠皮肤的形态发育变化;以K15单克隆抗体为一抗,进行免疫组织化学染色,观察K15在大鼠皮肤中的表达状况.结果(1)组织学方法显示,随着年龄的增长,大鼠背部表皮细胞层数逐渐变少;在毛囊的生长周期中,以隆突区为界,毛囊上段为恒定区,下段呈周期性变化(2)免疫组化染色显示,毛囊隆突区细胞胞浆表达K15,随年龄的增长,K15阳性细胞出现在毛母质细胞区、毛囊外根鞘和表皮基底层.结论表皮干细胞位于毛囊隆突区,与表皮的更新和毛囊的周期性变化有关.     

皮肤表皮干细胞的研究进展

成体的皮肤一生都在不断的自我更新,其中的毛囊还是保证毛发进行生长-脱落周期循环的细胞组织学基础。存在于表皮内的干细胞维持了成体皮肤的自我平衡及毛发再生。表皮是由构体分子组成。每个构体分子包含毛皮脂单位（毛囊和皮脂腺）及其周围的毛囊间表皮。毛囊间表皮具有祖细胞,损伤时能自我更新;毛囊具有多能干细胞,在新毛发周期开始或者损伤时能够启动干细胞功能,为毛囊的生长或表皮的修复提供细胞来源。本文概述了当前对表皮干细胞的认识,着重阐明毛囊间表皮内有祖细胞的证据,毛囊间表皮干细胞在体外的自我更新能力,毛囊膨突部内干细胞的特征和一些相关基因的表达等。     

小鼠皮肤及其毛囊早期发育的组织学观察

目的探讨小鼠皮肤及其毛囊的早期发育规律。方法采用常规石蜡切片和H-E染色技术,观察昆明系小鼠出生前后皮肤及其毛囊的形态发育。结果(1)孕龄16 d胎鼠的皮肤表面形成凹凸不平的深褶皱,但在生后3 d~5 d不仅皱褶的数量减少,而且凹陷变浅;(2)胎鼠孕龄16 d至19 d,其皮肤的表皮、真皮及皮肤总厚度呈现平稳增厚。但是,出生后,其表皮、真皮和皮肤总厚度急剧降低;在生后第1天至第9天,表皮呈现平稳增厚,而真皮则在生后快速厚度,第7天达到最高值(1861.50μm);(3)孕龄16 d的胎鼠皮肤中可观察到初级毛囊,至生后第7天其密度呈现平稳增长;与其相比,次级毛囊从18 d胎鼠开始出现,其密度增长非常迅速,出生后第7天达到1257.14/mm;毛囊的总密度与次级毛囊呈现相似的变化趋势。出生第7天后,由于毛囊的数量急剧增加,无法观察初级毛囊和次级毛囊的变化规律;(4)初级毛囊和次级毛囊的长度与深度变化在出生前后的相对缓慢,与其相比在第3天以后至第7天呈现迅速变化趋势。结论小鼠皮肤及其毛囊的生长性发育发生在胎儿晚期和生后的早期,而其周期性变化可能从出生后的第9天以后开始出现;在孕期16 d至生后第7天可能是检测毛囊特异性基因表达的最佳期。     

版纳鱼螈幼体和成体皮肤的结构

采用光镜和扫描电镜,对我国特有的珍稀濒危两栖动物版纳鱼螈Ichthyophis bannanicus幼体和成体的皮肤进行形态学和组织学观察.版纳鱼螈幼体和成体的皮肤均可分为表皮、真皮疏松层和真皮致密层;皮肤中含有粘液腺和颗粒腺;在不同发育阶段或同一个体的不同部位,其皮肤的各种组成成分在结构和厚度上存在着差异:成体和幼体都是头部的表皮最厚,尾部的最薄;幼体表皮各层细胞分化不明显,几无角化现象,成体表皮的各层细胞分化明显,表层细胞明显角化;成体躯干部皮肤最厚,头部最薄,幼体则是头部皮肤最厚,尾部最薄;幼体和成体的头部皮肤都分布有大量的粘液腺,颗粒腺分布较少;幼体的躯干部皮肤则主要分布着大量颗粒腺,尾部只有颗粒腺,未见粘液腺;成体躯干部和尾部皮肤均分布有大量的颗粒腺和粘液腺.     

麝鼠皮肤的显微结构特点

本文对４只成年野生麝鼠皮肤的显微结构进行了研究。其背、体侧皮厚于腹皮。体部针毛和绒毛呈簇分布，毛囊为复合笥，皮脂腺多沿毛囊群上部的周围分布，在观察的标本内未见汗朱分布。真皮下方紧贴一层皮肌。尾皮覆有鳞片，真皮较薄。     

石磺科3种贝类皮肤显微结构比较

应用石蜡切片和H.E染色技术,对石磺科(Onchidiidae)3个属的代表物种:瘤背石磺(Onchidium struma)、平疣桑椹石磺(Platevindex mortoni)和里氏拟石磺(Paraoncidium reevesii)的皮肤进行了组织学观察及参数测量比较。结果表明,3种石磺的皮肤虽然厚度不一,但基本结构相似,均由角质膜、表皮和真皮构成。角质膜是一层覆盖于表皮角质层上的蛋白质薄膜;表皮由多层上皮细胞构成,包括角质层、颗粒层和生发层;真皮包括疏松层和致密层,疏松层中嵌有颗粒腺和黏液腺两种腺体。3种石磺的皮肤厚度、各组织相对厚度及腺体数量等均存在差异。将结构差异与石磺的栖息环境进行比较分析后得到:陆栖为主的瘤背石磺皮肤表皮角质化程度高,颗粒腺发达;以水栖为主的里氏拟石磺表皮角质化程度相对低,黏液腺发达;而水陆两栖的平疣桑椹石磺,皮肤角质化程度介于前述二者之间,颗粒腺与黏液腺均不发达。研究结果体现了三者不同的生态适应特征,也为深入探讨海洋无脊椎动物从海洋向陆地进化的研究提供形态学依据。     

SD雌性大鼠性发育早期性器官等脏器和性激素的动态变化

目的探讨正常SD雌性大鼠性成熟前不同日龄段的脏器与促黄体生成素（LH）、促卵泡素（FSH）、雌二醇（E2）等性激素的变化及其关系。方法从生产群中取出60窝密度状态一致的SD大鼠,在不同日龄随机选取雌性大鼠,检测15、25、32、40日龄时大鼠体重、主要脏器指数,子宫、卵巢组织变化和15、25、32、40、60日龄大鼠血清LH、FSH、E2水平。结果记录了SD雌性大鼠性成熟前各脏器指数和卵巢、子宫组织变化,结果显示大鼠卵巢、子宫的增长速度大于体重的增长,而其他脏器增速大都小于体重的增长。本研究还记录了血清LH、FSH、E2水平在不同日龄段的变化规律,表明血清LH、E2浓度在32日龄时出现较为明显升高。结论不同日龄大鼠脏器指数的动态变化提示大鼠性器官在性发育早期得到机体的优先发育。血清LH、E2水平在32日龄时有了明显升高,提示性腺轴功能已经激活。60日龄大鼠血清性激素水平的波动类似于动情周期的规律性变化,推测大鼠在60日龄前即已进入性成熟,这些结果将为大鼠性发育的相关研究提供重要的参考数据。     

金佛拟小鲵幼体皮肤的显微结构观察

采用光镜和扫描电镜对金佛拟小鲵(Pseudohynobius jinfo)幼体皮肤进行组织学和形态学观察。金佛拟小鲵幼体皮肤由表皮和真皮构成。不同部位皮肤厚度不同,头部背侧皮肤最薄,其厚度为(45.99±12.77)μm,尾部腹侧的皮肤最厚,其厚度为(95.21±42.72)μm。表皮角质层仅躯干背部和尾部明显,由仍具有一定生理活性的复层扁平上皮细胞构成。皮肤腺体包括黏液腺和颗粒腺。黏液腺广泛分布于身体各个部位的皮肤,颗粒腺呈区域性分布,仅见躯干部和尾部皮肤,其体积大于黏液腺。毛细血管多分布于真皮疏松层腺体周围,与表皮层紧密接触并凸向表皮。色素细胞主要分布于表皮和疏松层的交界处,呈多细胞聚集的状态,形成厚度不一的色素层。     

Sparse and wavy hair: a new model for hypoplasia of hair follicle and mammary glands on rat chromosome 17

Mutant animals in the skin and hair have been used to identify important genes in biomedical research. We describe a new mutant rat, sparse and wavy hair (swh), that spontaneously arose in a colony of inbred WTC rats. The mutant phenotype was characterized by sparse and wavy hair, which was most prominent at age 3-4 weeks, and was inherited in an autosomal recessive manner. The swh/swh rats showed impaired gain of body weight, and their hair follicles were reduced both in number and size, associated with hypoplasia of the sebaceous glands and the subcutaneous fat tissue. Female swh/swh rats were unable to suckle their offspring. Their mammary glands were hypoplastic, and differentiation of mammary epithelial and myoepithelial cells was impaired. Linkage analysis of 579 backcross rats localized the swh locus to a .35-cM region between D17Rat131 and D17Rat50 in the distal end of rat Chr 17. The swh locus spanned the 3.7-Mb genomic region where 24 genes have been mapped and corresponded to the centromere region of the mouse Chr 2 or the region of the human Chr 10p11.1-p14. None of the genes or loci described in mouse or human hair and skin diseases mapped to these regions. These findings suggest that the rat swh is a novel mutation associated with impaired development of the skin appendages, such as hair follicles, sebaceous glands, and mammary glands, and will provide an experimental model to clarify a gene and mechanisms for development of skin appendages.     

Localization of sex steroid receptors in human skin

Sex steroid hormones are involved in regulation of skin development and functions as well as in some skin pathological events. To determine the sites of action of estrogens, androgens and progestins, studies have been performed during the recent years to accurately localize receptors for each steroid hormone in human skin. Androgen receptors (AR) have been localized in most keratinocytes in epidermis. In the dermis, AR was detected in about 10% of fibroblasts. In sebaceous glands, AR was observed in both basal cells and sebocytes. In hair follicles, AR expression was restricted to dermal papillar cells. In eccrine sweat glands, only few secretory cells were observed to express AR. Estrogen receptor (ER) alpha was poorly expressing, being restricted to sebocytes. In contrast, ERbeta was found to be highly expressed in the epidermis, sebaceous glands (basal cells and sebocytes) and eccrine sweat glands. In the hair follicle, ERbeta is widely expressed with strong nuclear staining in dermal papilla cells, inner sheath cells, matrix cells and outer sheath cells including the buldge region. Progesterone receptors (PR) staining was found in nuclei of some keratinocytes and in nuclei of basal cells and sebocytes in sebaceous glands. PR nuclear staining was also observed in dermal papilla cells of hair follicles and in eccrine sweat glands. This information on the differential localization of sex steroid receptors in human skin should be of great help for future investigation on the specific role of each steroid on skin and its appendages.     

Characterization of Hair Follicle Development in Engineered Skin Substitutes

Generation of skin appendages in engineered skin substitutes has been limited by lack of trichogenic potency in cultured postnatal cells. To investigate the feasibility and the limitation of hair regeneration, engineered skin substitutes were prepared with chimeric populations of cultured human keratinocytes from neonatal foreskins and cultured murine dermal papilla cells from adult GFP transgenic mice and grafted orthotopically to full-thickness wounds on athymic mice. Non-cultured dissociated neonatal murine-only skin cells, or cultured human-only skin keratinocytes and fibroblasts without dermal papilla cells served as positive and negative controls respectively. In this study, neonatal murine-only skin substitutes formed external hairs and sebaceous glands, chimeric skin substitutes formed pigmented hairs without sebaceous glands, and human-only skin substitutes formed no follicles or glands. Although chimeric hair cannot erupt readily, removal of upper skin layer exposed keratinized hair shafts at the skin surface. Development of incomplete pilosebaceous units in chimeric hair corresponded with upregulation of hair-related genes, LEF1 and WNT10B, and downregulation of a marker of sebaceous glands, Steroyl-CoA desaturase. Transepidermal water loss was normal in all conditions. This study demonstrated that while sebaceous glands may be involved in hair eruption, they are not required for hair development in engineered skin substitutes.     

Cidea Control of Lipid Storage and Secretion in Mouse and Human Sebaceous Glands

Sebaceous glands are skin appendages that secrete sebum onto hair follicles to lubricate the hair and maintain skin homeostasis. In this study, we demonstrated that Cidea is expressed at high levels in lipid-laden mature sebocytes and that Cidea deficiency led to dry hair and hair loss in aged mice. In addition, Cidea-deficient mice had markedly reduced levels of skin surface lipids, including triacylglycerides (TAGs) and wax diesters (WDEs), and these mice were defective in water repulsion and thermoregulation. Furthermore, we observed that Cidea-deficient sebocytes accumulated a large number of smaller-sized lipid droplets (LDs), whereas overexpression of Cidea in human SZ95 sebocytes resulted in increased lipid storage and the accumulation of large LDs. Importantly, Cidea was highly expressed in human sebaceous glands, and its expression levels were positively correlated with human sebum secretion. Our data revealed that Cidea is a crucial regulator of sebaceous gland lipid storage and sebum lipid secretion in mammals and humans.     

Microscopic observations of skin and lymphoid organs in the hairless dog derived from the Mexican hairless

The skin and lymphoid organs of Mexican hairless dogs and their hairless offspring were examined histologically. The hairless dogs lacked most hairs except for sparse hairs on the head, tail and feet. The skin of newborn pups consisted of a thick epidermis with epidermal ingrowths forming the rudiments of hair follicles. In older dogs more than 2 months of age, however, the epidermis was thin and the ingrowths were few. Neither hair follicles nor skin glands were present. The hairy skin of the head and tail had hair follicles with sebaceous glands. Regarding the lymphoid organs, the newborn pups possessed a thymus like haired pups. But in the older dogs more than 2 months of age, the thymus was atrophied and the lymphocyte population was too sparse to demarcate the cortex and the medulla. Lymphocyte accumulation in older dogs was also poor in the spleen and mesenteric lymph nodes. The present findings indicate that the hairlessness of the Mexican hairless dogs and their descendants is accompanied by early atrophy of the thymus after birth, and is followed by poor accumulation of lymphocytes in the thymus-dependent area of the spleen and the mesenteric lymph nodes. The defect of the thymus in the hairless dog seems to be different from that in athymic nude mice and rats. Further studies are needed to elucidate the immunological response and function in hairless dogs.     

Smad7-induced beta-catenin degradation alters epidermal appendage development

To assess whether Smad signaling affects skin development, we generated transgenic mice in which a Smad antagonist, Smad7, was induced in keratinocytes, including epidermal stem cells. Smad7 transgene induction perturbed hair follicle morphogenesis and differentiation, but accelerated sebaceous gland morphogenesis. Further analysis revealed that independent of its role in anti-Smad signaling, Smad7 bound beta-catenin and induced beta-catenin degradation by recruiting an E3 ligase, Smurf2, to the Smad7/beta-catenin complex. Consequently, Wnt/beta-catenin signaling was suppressed in Smad7 transgenic hair follicles. Coexpression of the Smurf2 and Smad7 transgenes exacerbated Smad7-induced abnormalities in hair follicles and sebaceous glands. Conversely, when endogenous Smad7 was knocked down, keratinocytes exhibited increased beta-catenin protein and enhanced Wnt signaling. Our data reveal a mechanism for Smad7 in antagonizing Wnt/beta-catenin signaling, thereby shifting the skin differentiation program from forming hair follicles to sebaceous glands.     

Innervation and cholinesterase activity in the skin of albino and desert rats

The distribution of nerves and cholinesterase activity in the skin of the desert and albino rats has been studied using both histological and histochemical techniques. In the desert rat, the skin was richly innervated. Specific cholinesterase was concentrated in the nervous network of the dermis and around the hair follicles, in the nerve bundles of the dermis, in perivascular nerves, in fine intra-epithelial nerves and in sensory end organs in the junctional area between the dermis and epidermis. In the albino rat, specific cholinesterase was concentrated in the sebaceous glands. The positive cholinesterase activity that was seen in the desert rat in intra-epithelial nerves, and in dermal and hair follicle networks could not be demonstrated.     

Cellular dynamics of the outer layers of the hair follicle of fine-wool sheep during the phase of stable hair growth

The structure, origin, and migration of outer sheath cells of the hair follicles of domestic sheep were studied by electron microscopic, autoradiographic, and histochemical (glycogen) methods in order to understand the role of this layer in hair morphogenesis. We demonstrated that the cells of the outer layers of the outer sheath interpose into the inner “companion” layer of the outer sheath. Although this process takes place all along the hair follicle from the lower bulb up to the sebaceous glands orifices, it mainly takes place over the bulb. Labeled cells interposed into the companion layer reach sebaceous glands orifices more than 24 h faster than labeled cells of the inner sheath and hair, because these cells included the label not in the bulb cambium (as hair and inner sheath) but over the bulb, and from this point they start movement. Interposition of cells into the companion layer must cause increase of its volume and additional volume supposed to be led away into the pillar canal around the hair near the sebaceous glands orifices. This can provide the mechanism of the hair and inner sheath promotion to sebaceous gland orifices.     

The skin of primates. XXIX. The skin of the pigmy bushbaby (Galago demidovii)

The skin of the pigmy bushbaby (Galago demidovii), the smallest existing prosimian, is largely similar to that of the other African Lorisidae, although this animal has certain peculiar features. The very thin epidermis contains alkaline phosphatase-reactive dendritic cells which resemble those in the other bushbabies and the potto. The hair follicles of this animal are similar to those of the lesser bushbaby, while the sebaceous glands are different from those of the other bushbabies in being reactive for alkaline phosphatase. The histological and histochemical properties of the sweat glands are similar to those of the other bushbabies.