Fourier Transform Infrared Imaging Analysis Research Articles

Fourier Transform Infrared Imaging Analysis of Interactions Between Polypropylene Grafted with Maleic Anhydride and Silica Spheres Using Two-Trace Two-Dimensional Correlation Mapping.

A technique for analyzing infrared imaging data based on two-trace two-dimensional (2T2D) correlation analysis is presented to extract pertinent information underlying spectroscopic imaging data. In 2T2D correlation mapping, each spectrum in hyperspectral data is individually compared with a reference spectrum to generate 2T2D asynchronous correlation intensity at the x- and y-coordinates on a 2T2D correlation map. Asynchronous correlation intensity develops only when the signal contribution from a certain species becomes even more significant in the sample spectrum compared with the reference spectrum. This feature can be advantageously utilized to examine molecular interaction or an intermediate form of the component present in a system of interest. 2T2D correlation mapping is examined using Fourier transform infrared imaging data of polymer composites based on polypropylene grafted with maleic anhydride melt-mixed with silica spheres. Infrared images derived by using conventional visualization based on a single wavenumber (i.e., 1713 cm-1) are dominated with the overwhelming infrared absorbance induced by the normal maleic anhydride species, making the identification of subtle but pertinent changes in the composite system difficult. A 2T2D correlation map derived from the maleic anhydride/silica spheres composite developed a significant asynchronous correlation intensity between the infrared bands at 1695 and 1713 cm-1 around a specific region on the map where the maleic anhydride and silica spheres coexist. On the other hand, such a correlation pattern becomes less acute when the silica spheres is modified with the octadecyldimethyl group to prevent the hydrogen bonding with the maleic anhydride. It thus revealed that the silanol groups on the surface of the silica spheres substantially interact with the maleic anhydride via the development of the hydrogen bonding.

Multiscale Synchrotron-Based Imaging Analysis for the Transfer of PEGylated Gold Nanoparticles In Vivo.

High spatial resolution imaging analysis is urgently needed to explore the biodistribution, transfer and clearance profiles, and biological impact of nanoparticles in the body, which will be helpful to clarify the efficacy of nanomedicine in clinical applications. Herein, by combination with multiscale synchrotron-based imaging techniques, including X-ray fluorescence (XRF) spectrometry, Fourier transform infrared (FTIR) spectroscopy, and micro X-ray phase contrast computed tomography (micro-XPCT), we visually displayed the transfer patterns and site-specific distribution of PEGylated gold nanoparticles (PEG-GNPs) in the suborgans of the liver, spleen, and kidney after an intravenous injection in mice. A combination of XRF and FTIR imaging analysis showed that the PEG bands presented similar distribution patterns with Au in the intraorgans, suggesting the stability of PEGylation on GNPs. We show that the PEG-GNPs presented heterogeneous distribution in the hepatic lobules with a large amount around the portal vein zone and then a gradient decrease in the sinusoidal region and the CV zone; in the spleen, it gradually accumulated in the splenic red pulp over time; and in the kidney, it quickly transported via the bloodstream to the renal pyramids and renal pelvis, and parts of PEG-GNPs finally accumulated in the renal medulla and renal cortex. Multidimensional micro-XPCT images further show that the PEG-GNP transfer in the liver induced hepatic blood vessel dilatation while they transferred in the liver, providing evidence of GNP transport across the blood vessel endothelial barrier.

Fourier-Transform Infrared Spectroscopy of Epiretinal Membranes and Internal Limiting Membranes after Pars Plana Vitrectomy with Membrane Peeling

Introduction: Fourier-transform infrared imaging (FTIRI) enables examination of protein secondary structure in the analyzed tissues. The aim of our study was to examine the distribution of secondary structures in epiretinal membranes (ERMs) and internal limiting membranes (ILMs), and to explore possible associations to other diagnostic variables. Methods: This prospective pilot study included patients scheduled for pars plana vitrectomy with membrane peeling. ERMs and ILMs were harvested during surgery and placed on a BaF₂ window for postsurgical FTIRI analysis. Infrared hyperspectral images were subjected to second and fourth derivative analysis to obtain information of the protein secondary structures present in the tissues. Results: Samples of 43 patients were analyzed, with the triple helical domain showing the highest prevalence in the examined tissues. The other secondary structures (beta-sheet, random coil, and beta-turn) showed a heterogenous distribution in the examined samples, without specific associations to indication of surgery, comorbidities, outcomes from optical coherence tomography, and intrasurgical findings. Conclusions: FTIRI enables analysis of the spatial distribution of protein secondary structures in the examined tissues; thus, it is a useful analytical technique for the analysis of ERMs and ILMs.

Molecular-Scale Deformation of Polypropylene/Silica Composites Probed by Rheo-Optical Fourier-Transform Infrared (FTIR) Imaging Analysis Combined with Disrelation Mapping.

We have developed a novel rheo-optical Fourier-transform infrared (FTIR) imaging technique that can probe the molecular-scale deformation behavior of a polymer matrix in composite materials. This rheo-optical FTIR imaging is based on in situ-polarized FTIR imaging of a polymer sample while it is being deformed by mechanical force. This imaging technique readily captures the orientation of the polymer molecules resulting from the applied strain. Analysis of the resulting FTIR imaging data by disrelation mapping makes it possible to further elucidate subtle but pertinent spectral variations arising from changes in the state of molecules within the spectroscopic images. In this study, the rheo-optical FTIR imaging is applied to analysis of the deformation behaviors of a composite composed of polypropylene containing hydroxyl groups (PPOH) and silica spheres (SS) to investigate matrix-filler adhesion of the composite. Our rheo-optical FTIR imaging analysis revealed selective inhibition of PPOH orientation at the matrix-filler interface during tensile deformation due to high matrix-filler adhesion via hydrogen bonding. The strong link between the PPOH matrix and SS filler efficiently restricts mobility of the matrix, resulting in the reinforcement of PPOH by addition of SS. Rheo-optical FTIR imaging is an effective tool for probing localized deformation behavior at the matrix-filler interface as well as achieving a better understanding of the correlation between matrix-filler adhesion and the effective reinforcement of composites.

Study of matrix-filler interaction of polypropylene/silica composite by combined infrared (IR) spectroscopic imaging and disrelation mapping

We demonstrate a Fourier transform infrared (FTIR) spectroscopic imaging combined with two-dimensional (2D) correlation analysis to elucidate matrix-filler interaction of polymer composites. Composite of maleic anhydride grafted polypropylene (MAPP) and silica sphere (SS) was fabricated. The FTIR image and disrelation map derived from sets of FTIR spectra suggest that the maleic anhydride groups in MAPP surround the SS surface and interact with the silanol on the surfaces of SS via hydrogen bonding. This clear link between MAPP and SS indicates that MAPP can be utilized as a suitable amphiphilic compatibilizer for an SS filler when it is mixed with hydrophobic polymer. FTIR imaging analysis was then further extended to categorize the interfacial states of more complicated polymer composites consisting of polypropylene (PP)/SS containing MAPP as a compatibilizer. Probing the interfacial chemical state using FTIR imaging revealed the interaction between MAPP and SS to contribute to improved elastic modulus of PP/MAPP/SS.

Dietary diisononylphthalate contamination induces hepatic stress: a multidisciplinary investigation in gilthead seabream (Sparus aurata) liver.

In this study, adult gilthead seabream (Sparus aurata) were exposed for 21days to Di-iso-nonylphthalte (DiNP at 15 and 1500μgkg-1bwday-1) via the diet. This plastic additive has been recently introduced to replace the di-(2-ethylhexyl)phthalate, the toxicity of which has been demonstrated conclusively both in vivo and in vitro trials. An analysis of a set of biomarkers involved in stress and immune response provides evidence of hepatic toxicity by DiNP in the present study. Both hsp70 and gr mRNA levels were upregulated significantly by DiNP, while plasma cortisol increased only in fish fed with the lowest DiNP dose. The oxidative stress markers g6pdh, glut red, gpx1 and CAT were upregulated by DiNP; gst mRNA was induced by the high dose and gck mRNA was downregulated significantly by the low dose. The mRNA levels of genes involved in the immune response, such as pla2, 5-lox, tnfa and cox2, were upregulated significantly only by the high dose of DiNP, while il1 mRNA increases in both doses. These molecular evidences were complemented with features obtained by Fourier Transform Infrared Imaging (FTIRI) analysis regarding the hepatic distribution of the main biological macromolecules. The FTIRI analysis showed an alteration of biochemical composition in DiNP samples. In particular, the low dose of DiNP induced an increase of saturated and unsaturated lipids and phosphorylated proteins, and a decrease of glycogen levels. The levels of caspase did not change significantly in the study, suggesting that DiNP does not activate apoptosis. Finally, the results also suggested the onset of hepatic oxidative stress and the activation of immune response, adding new knowledge to the already described hepatic DiNP toxicity.

FTIR imaging analysis of cell content in sea-ice diatom taxa during a spring bloom in the lower Northwest Passage of the Canadian Arctic

MEPS Marine Ecology Progress Series Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout the JournalEditorsTheme Sections MEPS 569:77-88 (2017) - DOI: https://doi.org/10.3354/meps12088 FTIR imaging analysis of cell content in sea-ice diatom taxa during a spring bloom in the lower Northwest Passage of the Canadian Arctic Nicole M. Pogorzelec1, C. J. Mundy1,*, Catherine R. Findlay2, Karley Campbell1, Aura Diaz1, Jens K. Ehn1, Søren Rysgaard1, Kathleen M. Gough2,* 1Centre for Earth Observation Science (CEOS), and 2Department of Chemistry, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada *Corresponding authors: cj.mundy@umanitoba.ca, kathleen.gough@umanitoba.ca ABSTRACT: During their vernal bloom, ice algae respond to variable light and nutrient availability by changing their production of cellular lipids and proteins. Fourier transform infrared (FTIR) spectrochemical imaging was used to quantify relative amounts of saturated lipids and proteins within algal cells from high and low light conditions, i.e. thin and thick snow cover, respectively. Samples were collected within the lower Northwest Passage, near Cambridge Bay, Nunavut, Canada during the 2014 ICE-CAMPS field campaign. Diatom taxa analyzed included Nitzschia frigida, pennate ribbon colonies, and Attheya spp. Saturated lipid content and lipid to protein ratios were significantly greater under thin snow covers relative to those under thick; cell protein content remained relatively stable throughout the study under both snow covers. Results have been interpreted relative to a concurrent, related study wherein under-ice nutrients were concluded to be limited throughout the study. Taxa responses reported herein differed according to size, with N. frigida exhibiting the earliest and most dramatic changes. The increase in lipid to protein ratio highlighted the transitioning allocation of carbon from protein to lipid algal biomass through the spring bloom progression, with increasing light under nutrient limiting conditions in this location. KEY WORDS: Arctic diatom · FTIR · Sea-ice algae · Light and nutrient limitation · Biomass composition · Proteins · Saturated lipids Full text in pdf format Supplementary material PreviousNextCite this article as: Pogorzelec NM, Mundy CJ, Findlay CR, Campbell K and others (2017) FTIR imaging analysis of cell content in sea-ice diatom taxa during a spring bloom in the lower Northwest Passage of the Canadian Arctic. Mar Ecol Prog Ser 569:77-88. https://doi.org/10.3354/meps12088 Export citation RSS - Facebook - Tweet - linkedIn Cited by Published in MEPS Vol. 569. Online publication date: April 07, 2017 Print ISSN: 0171-8630; Online ISSN: 1616-1599 Copyright © 2017 Inter-Research.

Fourier Transform Infrared Imaging analysis of dental pulp inflammatory diseases

Fourier Transform Infrared microspectroscopy let characterize the macromolecular composition and distribution of tissues and cells, by studying the interaction between infrared radiation and matter. Therefore, we hypothesize to exploit this analytical tool in the analysis of inflamed pulps, to detect the different biochemical features related to various degrees of inflammation. IR maps of 13 irreversible and 12 hyperplastic pulpitis, together with 10 normal pulps, were acquired, compared with histological findings and submitted to multivariate (HCA, PCA, SIMCA) and statistical (one-way ANOVA) analysis. The fit of convoluted bands let calculate meaningful band area ratios (means±s.d., P<0.05). The infrared imaging analysis pin-pointed higher amounts of water and lower quantities of type I collagen in all inflamed pulps. Specific vibrational markers were defined for irreversible pulpitis (Lipids/Total Biomass, PhII/Total Biomass, CH2 /CH3 , and Ty/AII) and hyperplastic ones (OH/Total Biomass, Collagen/Total Biomass, and CH3 Collagen/Total Biomass). The study confirmed that FTIR microspectroscopy let discriminate tissues' biological features. The infrared imaging analysis evidenced, in inflamed pulps, alterations in tissues' structure and composition. Changes in lipid metabolism, increasing amounts of tyrosine, and the occurrence of phosphorylative processes were highlighted in irreversible pulpitis, while high amounts of water and low quantities of type I collagen were detected in hyperplastic samples.

FTIR imaging detects diet and genotype-dependent chemical composition changes in wild type and mutant C. elegans strains.

This study focuses on the use of Fourier Transform Infrared (FTIR) microspectroscopy to determine chemical changes induced in the nematode Caenorhabditis elegans by supplementation of C. elegans maintenance media (CeMM) by Eicosapentaenoic acid (EPA). Wild-type C. elegans (N2) and mutant strains (tub-1 and fat-3) were grown in CeMM alone, and CeMM supplemented with EPA at 25 or 100 μM. Feeding was performed for 72 h. FTIR imaging was performed in transmission mode on individual worms. The FTIR imaging analysis of wild-type animals revealed the presence of vibrations assigned to unsaturated fatty acids, specifically bands at 3008 cm-1 ([double bond, length as m-dash]C-H, olefinic stretch) and 1744 cm-1 (C[double bond, length as m-dash]O, unsaturated fatty acids). It confirmed previously reported synthesis of unsaturated fatty acids in wild-type C. elegans. For the FTIR spectra of mutant strains, these vibrations were absent or present only as very small shoulder, which indicates that tub-1 and fat-3 synthesize essentially saturated fatty acids as indicated by the presence of -CH2 and C[double bond, length as m-dash]O vibrations. These results are in agreement with previous studies which reported that these mutants have altered lipid compositions. Principal component analysis showed differences in chemical composition between wild-type and mutant strains as well as between mutant strains cultured in normal CeMM and those cultured in CeMM supplemented with EPA. This study demonstrated the usefulness of FTIR microspectroscopy to investigate fat metabolism in C. elegans.

Bone mineral properties in growing Col1a2+/G610C mice, an animal model of osteogenesis imperfecta

The Col1a2+/G610C knock-in mouse, models osteogenesis imperfecta in a large old order Amish family (OOA) with type IV OI, caused by a G-to-T transversion at nucleotide 2098, which alters the gly-610 codon in the triple-helical domain of the α2(I) chain of type I collagen. Mineral and matrix properties of the long bones and vertebrae of male Col1a2+/G610C and their wild-type controls (Col1a2+/+), were characterized to gain insight into the role of α2-chain collagen mutations in mineralization. Additionally, we examined the rescuability of the composition by sclerostin inhibition initiated by crossing Col1a2+/G610C with an LRP+/A214V high bone mass allele. At age 10-days, vertebrae and tibia showed few alterations by micro-CT or Fourier transform infrared imaging (FTIRI). At 2-months-of-age, Col1a2+/G610C tibias had 13% fewer secondary trabeculae than Col1a2+/+, these were thinner (11%) and more widely spaced (20%) than those of Col1a2+/+ mice. Vertebrae of Col1a2+/G610C mice at 2-months also had lower bone volume fraction (38%), trabecular number (13%), thickness (13%) and connectivity density (32%) compared to Col1a2+/+. The cortical bone of Col1a2+/G610C tibias at 2-months had 3% higher tissue mineral density compared to Col1a2+/+; Col1a2+/G610C vertebrae had lower cortical thickness (29%), bone area (37%) and polar moment of inertia (38%) relative to Col1a2+/+. FTIRI analysis, which provides information on bone chemical composition at ~7μm-spatial resolution, showed tibias at 10-days did not differ between genotypes. Comparing identical bone types in Col1a2+/G610C to Col1a2+/+ at 2-months-of-age, tibias showed higher mineral-to-matrix ratio in trabeculae (17%) and cortices (31%). and in vertebral cortices (28%). Collagen maturity was 42% higher at 10-days-of-age in Col1a2+/G610C vertebral trabeculae and in 2-month tibial cortices (12%), vertebral trabeculae (42%) and vertebral cortices (12%). Higher acid-phosphate substitution was noted in 10-day-old trabecular bone in vertebrae (31%) and in 2-month old trabecular bone in both tibia (31%) and vertebrae (4%). There was also a 16% lower carbonate-to-phosphate ratio in vertebral trabeculae and a correspondingly higher (22%) carbonate-to-phosphate ratio in 2month-old vertebral cortices. At age 3-months-of-age, male femurs with both a Col1a2+/G610C allele and a Lrp5 high bone mass allele (Lrp5+/A214V) showed an improvement in bone composition, presenting higher trabecular carbonate-to-phosphate ratio (18%) and lower trabecular and cortical acid-phosphate substitutions (8% and 18%, respectively). Together, these results indicate that mutant collagen α2(I) chain affects both bone quantity and composition, and the usefulness of this model for studies of potential OI therapies such as anti-sclerostin treatments.

The effect of layered double hydroxides dispersion on thermal and mechanical properties of poly(vinyl chloride)/poly(methyl methacrylate) blends

AbstractPoly(vinyl chloride) (PVC)/layered double hydroxide (LDH) composites and PVC/poly(methyl methacrylate) (PMMA)/LDH composites were prepared via solution intercalation into PVC using both unmodified and organo‐modified LDHs and variable‐molecular‐weight PMMA as additional components. The LDH dispersion was investigated using X‐ray diffraction analysis and electron microscopy in scanning and transmission modes. Spotlight fourier transform infrared (FTIR) chemical imaging analysis was also used to obtain a deeper insight into the dispersion of polymer phases and LDH segregation. Thermal properties were determined using thermogravimetric analysis and differential scanning calorimetry; moreover, a preliminary investigation of mechanical properties in tensile mode and evaluation of the Vicat softening temperature were carried out. The morphological analysis of PVC/LDH and PVC/PMMA/LDH composites evidenced in both cases the presence of disordered micro‐aggregates with loss of the LDH crystallographic symmetry depending on the amount and molecular weight of PMMA. In particular, in the case of PVC/PMMA/LDH composites, the FTIR imaging analysis showed that PMMA mostly segregated in the LDH phase. However, even if the degree of LDH dispersion was not elevated (micro‐aggregates with disordered structures and size ranging from 0.5 up to 11 µm were evidenced), thermal stability and mechanical properties of the composites were improved with a synergic effect of PMMA and LDH. © 2013 Society of Chemical Industry

Fourier transform infrared imaging analysis in discrimination studies of squamous cell carcinoma

Oral squamous cell carcinoma (OSCC) of the oral cavity and oropharynx represents more than 95% of all malignant neoplasms in the oral cavity. Histomorphological evaluation of this cancer type is invasive and remains a time consuming and subjective technique. Therefore, novel approaches for histological recognition are necessary to identify malignancy at an early stage. Fourier transform infrared (FTIR) imaging has become an essential tool for the detection and characterization of the molecular components of biological processes, such as those responsible for the dynamic properties of tumor progression. FTIR imaging is a modern analytical technique enabling molecular imaging of a complex biological sample and is based on the absorption of IR radiation by vibrational transitions in covalent bonds. One major advantage of this technique is the acquisition of local molecular expression profiles, while maintaining the topographic integrity of the tissue and avoiding time-consuming extraction, purification, and separation steps. With this imaging technique, it is possible to obtain unique images of the spatial distribution of proteins, lipids, carbohydrates, cholesterols, nucleic acids, phospholipids, and small molecules with high spatial resolution. Analysis and visualization of FTIR imaging datasets are challenging and the use of chemometric tools is crucial in order to take advantage of the full measurement. Therefore, methodologies for this task based on the novel developed algorithm for multivariate image analysis (MIA) are often necessary. In the present study, FTIR imaging and data analysis methods were combined to optimize the tissue measurement mode after deparaffinization and subsequent data evaluation (univariate analysis and MIAs). We demonstrate that it is possible to collect excellent IR spectra from formalin-fixed paraffin-embedded (FFPE) tissue microarrays (TMAs) of OSCC tissue sections employing an optimised analytical protocol. The correlation of FTIR imaging to the morphological tissue features obtained by histological staining of the sections demonstrated that many histomorphological tissue patterns can be visualized in the colour images. The different algorithms used for MIAs of FTIR imaging data dramatically increased the information content of the IR images from squamous cell tissue sections. These findings indicate that intra-operative and surgical specimens of squamous cell carcinoma tissue can be characterized by FTIR imaging.

Fourier Transform Infrared Imaging Analysis of Cancellous Bone in Alendronate- and Raloxifene-Treated Osteopenic Sheep

Fourier transform infrared imaging spectroscopy (FTIRI)-assessed bone composition parameters (mineral content, collagen maturity, crystal size and perfection, and carbonate content) describe bone quality and correlate to bone fracture risk. The challenge with studying bone quality in patients treated with antiresorptive drugs such as bisphosphonates (e.g., alendronate) and selective estrogen receptor modulators (SERMs) (e.g. raloxifene) is being able to test bone mechanical performance and material properties pre- and posttreatment. The purpose of this study was to evaluate the FTIRI changes in a large animal model of osteoporosis (female sheep with dietary induced metabolic acidosis; MA). Previous studies have investigated the relationship between bone material properties and bone strength in humans and smaller animals and have shown that changes in compositional properties influence fracture risk. Here we characterize the MA model at 6 and 12 months, demonstrate the loss of bone and changes in compositional properties, and show that 6 months of treatment with both antiresorptives ameliorate the bone loss as assessed by bone mineral density and FTIRI. This preliminary data suggest that the MA sheep model allows investigation of whether drug treatments preserve bone properties that exist at the time of treatment or if they induce further beneficial changes.

Bone Quality determined by Fourier Transform Infrared Imaging Analysis in Mild Primary Hyperparathyroidism

Mild primary hyperparathyroidism (PHPT) is characterized by asymptomatic hypercalcemia, most commonly in the absence of classical signs and symptoms. Hence, there is need to characterize this disorder with particular attention to the skeleton. We determined the ratio of pyridinium and dehydrodihydroxylysinonorleucine collagen cross-links in 46 iliac crest bone biopsies from patients with PHPT (14 men, aged 28-68 yr; 32 women, aged 26-74 yr) by Fourier transform infrared imaging. The results were compared with previously reported collagen cross-links ratio determined in iliac crest biopsies from normal subjects. PHPT patients exhibited significantly lower pyridinium to dehydrodihydroxylysinonorleucine collagen cross-links ratio, compared with normal controls. Parathyroidectomy restored values to those comparable with normal controls. Moreover, the differences among PHPT subjects were gender dependent, with female PHPT patients having a statistically significant lower ratio, compared with either male PHPT patients or normal controls. Comparison of the obtained outcomes with histomorphometry showed that the collagen cross-link ratio was strongly correlated with rate of bone formation, and mineralizing surface, in individual patients. This ratio was also correlated with bone mineralization density distribution parameters obtained in the same patients. The strongest correlations were with bone mineralization density distribution variables reflecting heterogeneity of mineralization and primary mineralization parameters. The results are consistent with the high turnover state manifested in PHPT patients. Reduced collagen cross-link ratio in patients with PHPT would be expected to reduce the stiffness of bone tissue. These observations provide a more complete assessment of bone material properties in this disorder.

A Fourier transform infrared microspectroscopic imaging investigation into an animal model exhibiting glioblastoma multiforme

Glioblastoma multiforme (GBM) is a highly malignant human brain tumour for which no cure is available at present. Numerous clinical studies as well as animal experiments are under way with the goal being to understand tumour biology and develop potential therapeutic approaches. C6 cell glioma in the adult rat is a frequently used and well accepted animal model for the malignant human glial tumour. By combining standard analytical methods such as histology and immunohistochemistry with Fourier Transform Infrared (FTIR) microspectroscopic imaging and multivariate statistical approaches, we are developing a novel approach to tumour diagnosis which allows us to obtain information about the structure and composition of tumour tissues that could not be obtained easily with either method alone. We have used a “Stingray” FTIR imaging spectrometer to analyse and compare the compositions of coronal brain tissue sections of a tumour-bearing animal and those from a healthy animal. We have found that the tumour tissue has a characteristic chemical signature, which distinguishes it from tumour-free brain tissue. The physical-chemical differences, determined by image and spectral comparison are consistent with changes in total protein absorbance, phosphodiester absorbance and physical dispersive artefacts. The results indicate that FTIR imaging analysis could become a valuable analytic method in brain tumour research and possibly in the diagnosis of human brain tumours.

Effects of transforming growth factor-β deficiency on bone development: A Fourier Transform-Infrared imaging analysis

Transforming growth factor-beta 1 (TGF-β1) is a cytokine member of the TGF-β superfamily involved in the control of proliferation and differentiation of various cell types. TGF-β1 plays an important role in bone formation and resorption. To determine the effect of TGF-β1 deficiency on bone mineral and matrix, tibias from mice in which TGF-β1 expression had been ablated (TGF-β1 null) were analyzed and compared with background- and age-matched wild-type (WT) control animals by Fourier transform-infrared imaging (FTIRI) and histochemistry. FTIRI allows the characterization of nondemineralized thin tissue sections at the ultrastructural level with a spatial resolution of ∽7 μm. The spectroscopic parameters calculated were: mineral-to-matrix ratio (previously shown to correspond to ash weight); mineral crystallinity (related to the crystallographically determined crystallite size and perfection in the apatite c-axis direction); and collagen maturity (related to the ratio of pyridinoline:deH-DHLNL collagen cross-links). Several fields were selected to represent different stages of bone development within the same specimen from the secondary ossification center to the distal diaphysis. Anatomically equivalent areas were compared as a function of age and genotype. The spectroscopic results were expressed both as color-coded images and as pixel population distributions for each of the three parameters monitored. Based on comparisons of histochemistry and FTIRI, there were distinctive age and genotype variations. At all ages examined, in the TGF-β1 null mice growth plates, alkaline phosphatase (ALP) activity and collagen maturity were reduced, but no effect on mineral content or crystallinity was noted. In the TGF-β1 null mice metaphyses, there was a persistence of trabeculae, but no significant alterations in mineral content or crystallinity. In contrast, mineral content, mineral crystallinity, and collagen maturity were reduced in the secondary ossification center and cortical bone of the TGF-β1 null mice. These results, consistent with a mechanism of impaired bone maturation in the TGF-β1 null mice, may be directly related to TGF-β1 deficiency and indirectly to increased expression of inflammatory cytokines in the TGFβ1 null mice.