Raman spectroscopy detects melanoma and the tissue surrounding melanoma using tissue-engineered melanoma models

Invasion of melanoma cells from the primary tumor involves interaction with adjacent tissues and extracellular matrix. The extent of this interaction is not fully understood. In this study Raman spectroscopy was applied to cryo-sections of established 3D models of melanoma in human skin. Principal component analysis was used to investigate differences between the tumor and normal tissue and between the peri-tumor area and the normal skin. Two human melanoma cells lines A375SM and C8161 were investigated and compared in 3D melanoma models. Changes were found in protein conformations and tryptophan configurations across the entire melanoma samples, in tyrosine orientation and in more fluid lipid packing only in tumor dense areas, and in increased glycogen content in the peri-tumor areas of melanoma. Raman spectroscopy revealed changes around the perimeter of a melanoma tumor as well as detecting differences between the tumor and the normal tissue.     

Magnetic resonance imaging of the penis: normal anatomy

This study was undertaken to investigate the magnetic resonance anatomy of the normal penis, by means of the use of a new designed surface coil specific for the study of male external genital organs. The combined evaluation of T1- and T2-weighted images obtained by choosing different repetition and echo time values together with an appropriate selection of scanning planes oriented according to various angles of incidence strongly contributed to perform a complete morphological analysis of the penis and constantly revealed fine anatomical details of diagnostic and clinical significance. Among these, the magnetic resonance examination (data referred to a 0.5 T apparatus) allowed a precise morphological differentiation of the penile covering tissues, such as outer skin, dartos tunica and hypodermal connective; the vascular characterization of cavernous tissue, belonging to corpora cavernosa and spongiosum urethrae, of deep arteries and superficial dorsal vein(s); the resolution of the albuginea and the identification of the urethral lumen. Such a capability of magnetic resonance imaging in providing accurate demonstration of penile structures without technical artifacts and use of ionizing radiations makes the actual technology able to cooperate efficaciously with computerized tomography and diagnostic sonography for an efficient clinical assessment of penis diseases.     

Strategies and results of atomic force microscopy in the study of cellular adhesion

Atomic Force Microscopy (AFM) provides a range of strategies for investigating living cell adhesion to the extracellular matrix, other cells or biomaterials in their native environment. This review surveys the results obtained from major studies using AFM for mechanical force evaluation in the cell, morphological visualization of the cell and studies of the cell's response to chemical or mechanical stress. Recently, the use of AFM has been broadened to obtain experimental information about cell adhesion molecules. Quantitative measurements of binding forces between adhesion proteins and their ligands in the cell or on a surface are presented. These analyses provide data on individual molecules and their resulting collective behaviour at the cell level. They significantly contribute to the characterisation of cellular adhesion with physical principles relating to biochemistry.     

Differentiating keloids from normal and hypertrophic scar based on multiophoton microscopy

We use a novel nonlinear optical technique, multiphoton microscopy, to differentiate keloids from hypertrophic and normal scars through the morphological and quantitative analysis of collagen and elastin in superficial dermis of scar tissues and boundary between normal skin and scar tissue.     

Picrosirius-polarization staining method as an efficient histopathological tool for collagenolysis detection in vesical prolapse lesions

The Picrosirius-polarization method has been indicated as a selective histochemical stain for collagen detection in tissue sections. This method can also be of value for studying collagen degradation given that, under polarized light, collagen displays birefringence due to its molecular order. The aim of this study is to highlight this staining method as an additional instrument for a rapid and excellent confirmatory diagnosis of the presence of collagenolysis in connective tissue in the vaginal wall with vesical prolapse lesion, in tissue sections. Dramatic changes in collagen morphology were found in vaginal mucosa in vesical prolapse disorder: they were weakly stained by Sirius red and under polarized light appeared as thin, pale (weakly birefringent), greenish, and with fibers more scattered, while the histoarchitecture of the organ showed a disrupted appearance. Thus, in the present study, we showed in vaginal mucosa in the vesicle prolapse that corroded collagenous framework appears as fragmentary and irregularly separated collagenous structures, that are weakly birefringent, corresponding to a molecular disorganization of these fibers caused by collagenolysis.     

Texture analysis of multiple sclerosis: a comparative study

The difficulty of using magnetic resonance imaging (MRI) to support early diagnosis of multiple sclerosis (MS) stems from the subtle pathological changes in the central nervous system (CNS). In this study, texture analysis was performed on MR images of MS patients and normal controls and a combined set of texture features were explored in order to better discriminate tissues between MS lesions, normal appearing white matter (NAWM) and normal white matter (NWM). Features were extracted from gradient matrix, run-length (RL) matrix, gray level co-occurrence matrix (GLCM), autoregressive (AR) model and wavelet analysis, and were selected based on greatest difference between different tissue types. The results of the combined set of texture features were compared with our previous results of GLCM-based features alone. The results of this study demonstrated that (1) with the combined set of texture features, classification was perfect (100%) between MS lesions and NAWM (or NWM), less successful (88.89%) among the three tissue types and worst (58.33%) between NAWM and NWM; (2) compared with GLCM-based features, the combined set of texture features were better at discriminating MS lesions and NWM, equally good at discriminating MS lesions and NAWM and at all three tissue types, but less effective in classification between NAWM and NWM. This study suggested that texture analysis with the combined set of texture features may be equally good or more advantageous than the commonly used GLCM-based features alone in discriminating MS lesions and NWM/NAWM and in supporting early diagnosis of MS.     

Characteristics of light scattering by normal and modified areas of skin tissue

Results from numerical calculations and experimental studies of the optical backscattering coefficients and changes in the polarization characteristics of normal and modified (birthmark, scar) skin tissue structures are presented. It is shown that determining the Mueller matrix is an effective way of detecting changes in the structure of skin tissue in vivo which reflects changes in the depolarization of light by an object for different polarization parameters of the incident (probe) radiation. The depolarization of light is found to be symmetric for normal areas of skin and antisymmetric for skin tissue with a modified structure. It is proposed that the polarization characteristics of scattered radiation be used in detecting damaged areas of skin tissue.     

Monitoring of mechanical properties of serially passaged bovine articular chondrocytes by atomic force microscopy

Atomic force microscopy (AFM) is a powerful tool in imaging cells and tissues and probing their mechanical properties. Articular chondrocytes, the cells responsible for the production and maintenance of cartilaginous extracellular matrix in the knee joint, change their morphology and dedifferentiate during in vitro expansion culture. It was unclear if the mechanical properties of chondrocytes change accompanying phenotype variation. The elasticity of in vitro serially cultured bovine articular chondrocytes was investigated using AFM. The chondrocytes changed their morphology from round to spindle-like. The freeze-dried P0 chondrocytes showed significantly higher modulus than did the serially passaged (P1–P4) chondrocytes. The change of chondrocyte morphology was accompanied with a decrease of elastic modulus.     

Fibrillin-rich microfibrils of the extracellular matrix: ultrastructure and assembly.

Fibrillin-rich microfibrils are a unique class of extensible connective tissue macromolecules. Their critical contribution to the establishment and maintenance of diverse extracellular matrices was underlined by the linkage of their principal structural component fibrillin to Marfan syndrome, a heritable connective tissue disorder with pleiotropic manifestations. Microscopy and preparative techniques have contributed substantially to the understanding of microfibril structure and function. The supramolecular organisation of microfibrillar assemblies in tissues has been examined by tissue sectioning and X-ray diffraction methods. Published findings are discussed and new information reported on the organisation of microfibrils in the ciliary zonular fibrils by environmental scanning electron microscopy. This review summarises microscopy and X-ray diffraction studies that are informing current understanding of the ultrastructure of fibrillin-rich microfibrils.     

乳腺组织形态基元共焦显微拉曼光谱的研究

利用共焦显微拉曼方法,测定了乳腺组织切片的Mapping拉曼谱,光谱采样体积达到μm尺度.通过对这些共焦拉曼谱与商业提纯肌动蛋白、胶原等生化物质做出的谱的分析比较,分离出了来自细胞质、细胞间质、脂肪以及乳腺沉积物这些组织形态基元的拉曼谱;用K阶簇分析方法,还获得了细胞核基元谱;基元谱与提纯化学物质谱的相关分析印证了组织形态基元谱的来源.还分析总结了这些组织形态基元谱的特征.这些工作为深入理解组织形态与其拉曼谱的关系以及乳腺组织形态拉曼模型的建立奠定了基础.     

ICP-MS法研究重度烧伤患者创面肉芽组织中微量元素的亚细胞分布

利用八极杆碰撞反应池(ORS)技术的电感耦合等离子体质谱(ICP-MS)法研究了Cr,Mn,Fe,Co,Cu,Zn,Se,Cd等元素在重度烧伤患者创面肉芽组织中的亚细胞分布。采用差速分级离心技术将样品分离获得细胞核、线粒体、溶酶体、微粒体和细胞上清液等亚细胞组分,使用混合酸HNO₃+H₂O₂并结合密闭微波消解对各亚细胞组分进行消解,分别选用ORS的氦碰撞模式和氢反应模式校正了质谱分析过程中的多原子离子干扰,以Rh为内标元素校正了基本效应和信号漂移现象。各待测元素的检出限在0.72～33.05 ng·L-1之间,相对标准偏差(RSD)小于8.4%。采用ORS-ICP-MS法可实现重度烧伤患者创面肉芽组织中微量元素亚细胞分布的准确分析,并可广泛应用于其他生物样品的分析,多数元素在创面肉芽组织和正常皮肤组织亚细胞组分的分布中存在显著性差异。     

Raman analysis of proteoglycans simultaneously in bone and cartilage

Bone and cartilage are connective tissues with distinct organic matrix (collagen and non‐collagenous proteins) composition facilitating their biological function. Proteoglycans (PGs), a member of the non‐collagenous proteins fulfill functions that are determined by both their core protein and their glycosaminoglycan chains. The purpose of the present study was to identify Raman bands that are representative of PG concentration and may be used in both bone and cartilage tissues. To achieve this goal, we analyzed a series of reference PGs and collagens, as well as turkey leg tendon to verify the laser polarization independency of the identified bands. Additionally, the applicability of these bands in both cartilage and bone tissue simultaneously was tested in a healthy femoral head by Raman imaging and hierarchical cluster analysis to describe the distribution of PGs at the micron level from articular cartilage to subchondral bone. The results of the study show that the Raman band ~1375 cm⁻¹ can be used as a PGs marker band in both cartilage and bone. Moreover, articular cartilage has a lower content of organic matrix (mostly type II collagen), while the middle and deep transitional zone haves a higher concentration of PGs. The calcified cartilage is characterized by a lower content of PGs and total organic matrix (estimated from the integrated area of the amide III band). Copyright © 2014 John Wiley & Sons, Ltd.     

Interaction of human gingival fibroblasts with PVA/gelatine sponges

Tissue engineering scaffolds should be able to reproduce optimal microenvironments in order to support cell attachment, three-dimensional growth, migration and, regarding fibroblasts, must also promote extracellular matrix production. Various bioactive molecules are employed in the preparation of spongy scaffolds to obtain biomimetic matrices by either surface-coating or introducing them into the bulk composition of the biomaterial. The biomimetic properties of a spongy matrix composed of PVA combined with the natural component gelatine were evaluated by culturing human gingival fibroblasts on the scaffold. Cell adhesion, morphology and distribution within the scaffold were assessed by histology and electron microscopy; viability and metabolic activity as well as extracellular matrix production were analyzed by MTT assay, cytochemistry and immunocytochemistry. Fibroblasts interacted positively with PVA/gelatine. They adhered to the PVA/gelatine matrix in which they had good spreading activity and active metabolism; fibroblasts were also able to produce extracellular matrix molecules (type I collagen, fibronectin and laminin) compared to bi-dimensionally grown cells. The in situ creation of a biological matrix by human fibroblasts together with the ability to produce growth factor TGF-beta1 and the intracellular signal transduction molecule RhoA, suggests that this kind of PVA/gelatine sponge may represent a suitable support for in vitro extracellular matrix production and connective tissue regeneration.     

Biophysical characteristics of cells cultured on cholesteryl ester liquid crystals

This study aimed at examining the biophysical characteristics of human derived keratinocytes (HaCaT) cultured on cholesteryl ester liquid crystals (CELC). CELC was previously shown to improve sensitivity in sensing cell contractions. Characteristics of the cell integrin expressions and presence of extracellular matrix (ECM) proteins on the liquid crystals were interrogated using various immunocytochemical techniques. The investigation was followed by characterization of the chemical properties of the liquid crystals (LC) after immersion in cell culture media using Fourier transform infrared spectroscopy (FTIR). The surface morphology of cells adhered to the LC was studied using atomic force microscopy (AFM). Consistent with the expressions of the integrins α2, α3 and β1, extracellular matrix proteins (laminin, collagen type IV and fibronectin) were found secreted by the HaCaT onto CELC and these proteins were also secreted by cells cultured on the glass substrates. FTIR analysis of the LC revealed the existence of spectrum assigned to cholesterol and ester moieties that are essential compounds for the metabolizing activities of keratinocytes. The immunostainings indicated that cell adhesion on the LC is mediated by self-secreted ECM proteins. As revealed by the AFM imaging, the constraint in cell membrane spread on the LC leads to the increase in cell surface roughness and thickness of cell membrane. The biophysical expressions of cells on biocompatible CELC suggested that CELC could be a new class of biological relevant material.     

Investigation of the influence of cell density of human fibroblasts cryopreserved inside collagen sponges at various cooling rates

The influence of cell density of cells cryopreserved inside a collagen matrix at various cooling rates was investigated. Human fibroblasts were three-dimensionally cultured for 2 days in a collagen sponge (20 mm in diameter and 1 mm in thickness) as an extracellular matrix to imitate biological tissue (artificial tissue). Different cell densities for the artificial tissue were used, from 10(5) to 10(7) cells/cm(3). Four artificial tissues were first stacked in a test chamber, frozen at a cooling rate of 0.3 to 50 degrees C/min in a solution of Dulbecco's Modified Eagle Medium, 20% fetal bovine serum and 10% dimethylsulfoxide, kept frozen below -185 degrees C for 2 hours, and then finally thawed. Membrane integrity of fibroblasts using a trypan blue exclusion assay was evaluated as an index for post-thaw cellular viability. Results show that with increasing cell density, the post-thaw membrane integrity decreased. Therefore, in the cryopreservation of biological tissue, it seems high cell density is one factor which causes a decline in viability.     

Histochemistry of skin glands of Trachycephalus aff. venulosus Laurenti, 1768 (Anura, Hylidae)

The skin of the adult tree frog, Trachycephalus aff. venulosus, was investigated by light microscopy. Histochemistry was carried out using various stain techniques and showed the basic integument morphology of the skin with squamous epithelium in the epidermis and connective tissue in the dermis, subdivided into spongy and compact layers. The integument observed contains two types of gland; the mucous glands and granular glands. The mucous glands are small and located in the upper layer of the stratum spongiosum of the connective tissue and contain neutral and acid sulfated glycoproteins. The granular glands are large and form a syncytial secretory compartment within the acinus, which is surrounded by smooth muscle cells. Histochemical analyses demonstrated the presence of collagen proteins in both types of gland. An unusual finding was the different densities of the granules in the granular glands. The morphological characteristics of the integument in Trachycephalus aff. venulosus was also compared with others species of Anura.     

Determination of Ca,Fe, Cu and Zn and their correlations in breast cancer and normal adjacent tissues

An experimental procedure using monoenergetic Synchrotron Radiation x‐ray Fluorescence (SR‐XRF) method was studied, justified and applied to determine trace elements concentrations of normal and neoplastic human breast tissues in the same individual. Scattered radiation from each sample was used as an internal standard in x‐ray emission spectroscopy in order to construct calibration curves used to determine Ca, Fe, Cu and Zn concentrations in 52 breast tissue specimens (26 neoplastic and 26 adjacent normal tissues). This work showed that this experimental alternative is approximately matrix independent and also allows a reduction in instrumental variables. Our results showed, as expected, that Ca, Fe, Cu and Zn concentrations levels were significantly higher in neoplastic than in healthy breast tissues (all p < 0.001). It was also observed that Fe and Cu levels are correlated in malignant breast tissues as well as Ca and Zn levels, indicating that these elements' concentrations are related, in agreement with the hypothesis that there is a connection between Fe and Cu with both increased cellular activity and blood supply in the formation of neoplasies in breast tissue, and between Ca and Zn as regulators of neoplasies growth, since these metals are present in active matrix metalloproteinases (MMPs). Copyright © 2008 John Wiley & Sons, Ltd.     

Atomic Force Microscopy of bulk tendon samples: affect of location and fixation on tissue ultrastructure

Atomic Force Microscopy (AFM) is a surface characterisation technique which analyses topology. To date, AFM studies of tissue ultrastructure have focussed on single collagen fibrils extracted from different tissues prior to analysis. Using sample preparation techniques used in electron microscopy studies, this work uses AFM to analyse the collagen ultrastructure of bulk samples from bovine deep digital flexor tendons (DDFTs). DDFT ultrastructure in regions of the tendon which experience different loading conditions are compared. Samples are analysed post-freezing and post-aldehyde fixation with either 10% formalin or 4% glutaraldehyde in order to investigate the affect of tissue preservation on tissue ultrastructure. The results demonstrate that both fibril diameter and repeat unit of the tendon vary between different regions in the dorsoventral plane, with regions subjected to both tensile and compressive forces exhibiting smaller fibril diameter and repeat unit compared to regions subjected to tensile forces alone. These differences are detectable regardless of the tissue preservation technique used. However these measured differences do vary with preservation techniques with aldehyde-fixed samples exhibiting smaller fibril diameters and larger repeat units compared to frozen samples. These results demonstrate that AFM is a highly suitable technique for the characterisation of different ultrastructures in bulk samples but that it is important to be consistent in the choice of preservation technique.     

结直肠组织中脂类的拉曼光谱研究

利用共聚焦显微拉曼光谱系统,检测了结直肠癌组织及邻近正常组织的拉曼光谱234例,从分子水平探讨结直肠癌变的原因。实验结果表明：在900～2 100 cm-1频移范围内,与正常组织比较,归属于结直肠癌组织中脂类伸缩振动的1 067和1 133 cm-1 拉曼峰强度相对较弱,扭转振动的1 299 cm-1与CH面内变形振动的1 264 cm-1拉曼峰的强度比值减少,应用SPSS16.0统计学软件进行平均值计算与比较,正常组织中的1 299和1 264 cm-1的强度比值平均值为3.17,癌变组织的为1.33; 二者的分界值为1.96,以此判别结直肠癌组织和正常组织符合率为94%。研究表明,结直肠癌组织中脂类的链内纵向有序性下降,不饱和度增加。可推测结直肠癌组织中脂类的能量储存增加是引起这些变化的原因,而这些变化将导致细胞膜的流动性增强,从而改变细胞膜的物质运输、能量传递和信号传导,终将引起DNA 结构的变化。因此,脂类的能量分布变化可能是导致细胞癌变的原因之一。