Orcein-Alcian Blue Staining: a New Technique for Demonstrating Acid Mucins in Gastrointestinal Epithelium

Total Page:16

File Type:pdf, Size:1020Kb

Orcein-Alcian Blue Staining: a New Technique for Demonstrating Acid Mucins in Gastrointestinal Epithelium J Clin Pathol: first published as 10.1136/jcp.42.8.881 on 1 August 1989. Downloaded from J Clin Pathol 1989;42:881-884 Orcein-alcian blue staining: a new technique for demonstrating acid mucins in gastrointestinal epithelium R SINGH, A W P GORTON Department ofHistopathology, Manor Hospital, Walsall, West Midlands SUMMARY Orcein-alcian blue staining, a new method for the simultaneous demonstration of sulphated and sialomucins in gastrointestinal epithelium was compared with the standard high iron diamine-alcian blue technique. Sections were oxidised with potassium permanagate and decolourised in oxalic acid. They were stained with orcein for four hours, differentiated for a few seconds in acid alcohol, and then counterstained with alcian blue for halfto one minute. There was a good correlation of results between the two methods. Orcein-alcian blue is a safer, cheaper, and quicker method than high iron diamine-alcian blue which can be safely introduced into routine laboratories for the study of acid mucins in the gastrointestinal diseases. Orcein, a naturally occurring vegetable dye, has been Table used for staining elastic fibres for many years. It is also used for the demonstration of hepatitis B antigen and Histological diagnosis No ofcases copper-associated proteins in chronic liver diseases.'2 copyright. Recently, the orcein technique has been studied for Normal mucosa (stomach, ileum, appendix, large bowel) 25 Intestinal metaplasia of stomach 5 showing the presence of sulphated mucin in gastroin- Adenomas (stomach, appendix, large bowel) 6 testinal epithelium.34 It has also been reported to be Adenocarcinomas (stomach, appendix, ileum, large bowel) II selectively positive for mucin-producing adenocarcin- Total 47 omas of the lower gastrointestinal tract; therefore, adenocarcinomas in sites other than the colon and rectum are negative for orcein staining.5 We report our BDH Poole, Dorset) in 100 ml 70% alcohol and then http://jcp.bmj.com/ findings of combining a modified orcein staining adding 1-0 ml concentrated hydrochloric acid. Sec- method with alcian blue to show the presence of tions were washed well in tap water and differentiated sulphated and sialomucins in normal, non-neoplastic, for a few seconds in acid-alcohol. Sections were again and neoplastic gastrointestinal epithelium. washed in water and stained in 1% alcian blue in 3% acetic acid (pH 2-5) for one minute. This was followed Material and methods by dehydration, clearing and mounting. The details of the 47 cases studied are shown in the CONTROL STUDY on September 28, 2021 by guest. Protected table. The resected surgical specimens were fixed in To establish that orcein stained sulphomucins in the 10% formol-saline and routinely processed for paraf- goblet cells and not sulphur-containing amino acids, fin wax embedding. Serial sections, 5 um thick, were control sections of keratinised skin, normal stomach, stained with haematoxylin and eosin, orcein, orcein- colon and rectum were subjected to a two stage alcian blue, high iron-diamine and high iron-diamine- blocking technique before orcein-alcian blue staining, alcian blue (modifications of Spicer's method).6 using sodium dithionite and mercuric chloride which Shikata's orcein method was used with a slight effectively block any S-S and S-H groups which might modification.' The sections were taken to water, then be present. The presence of such sulphur-containing oxidised in a solution of 0-25% potassium perman- amino acids can then be determined by comparison agate in 0-25% concentrated sulphuric acid for one with untreated, stained duplicate sections (HC Cook, minute. Sections were decolourised in 2% oxalic acid personal communication). and rinsed in water. They were then stained in orcein solution for four hours. This staining solution was Results prepared by dissolving 1-0 g natural orcein (Gurr, Accepted for publication 2 February 1989 Throughout the entire gastrointestinal tract, the 881 J Clin Pathol: first published as 10.1136/jcp.42.8.881 on 1 August 1989. Downloaded from 882 Singh, Gorton * .4 140-4.- A"iR.ci --i "I5I 'o* 4Wi: 'p 4A X~ ;, ' ; I- _ -. copyright. Fig 1 Section showing goblet cells ofstomach intestinal Fig 2 Section ofterminal ileum showing ocassional goblet metaplasia containing sulphated mucin (brown) and cells in the villi and crypts containing sulphomucin (brown). sialomucin (blue). (Orcein-alcian blue.) (Orcein-alcian blue.) goblet cells containing sulphated mucins stained were similar to that obtained with high iron diamine- http://jcp.bmj.com/ brown with orcein and sialomucins stained blue with alcian blue. alcian blue. With the exception of the elastic fibres, all The six benign and 11 malignant tumours stained other cells and tissues showed a faint brown staining with orcein-alcian blue and high iron diamine-alcian that was regarded as negative in this study. To blue had identical results. The benign tumours showed compare the staining results of orcein-alcian blue and a production of mixed mucins with predominance of high iron diamine-alcian blue identical areas were either sulphated or sialomucins. The malignant studied in serial sections. tumours varied from well differentiated mucin-secret- on September 28, 2021 by guest. Protected Surface foveolar epithelial cells of the stomach did ing to poorly differentiated with a corresponding not stain. Apical granules of the parietal cells of decrease in mucin content. The secretory product in all stomach showed a faint brown staining with orcein- the adenocarcinomas was a mixture of mucins with alcian blue. There was comparable negative staining of predominance of either sulphated or sialomucin. The cells with high iron diamine-alcian blue. The goblet poorly differentiated adenocarcinomas showed scanty cells in gastric intestinal metaplasia-complete and mucin in occasional goblet cells and in the lumen of incomplete type-however, stained for both sulphated gland-like structures. In mucoid carcinomas with and sialomucins (fig 1). High iron diamine-alcian blue extracellular mucin "lakes", however, there was a also showed similar results. In the terminal ileum, predominance of intra- and extracellular sialomucin close to the ileocaecal valve, traces of sulphomucins and little sulphomucin production. The sections were seen in occasional goblet cells (fig 2). In the left treated with dithionite stained with orcein-alcian blue colon sulphomucins were seen in the goblet cells in the showed undiminished staining in the goblet cells. The lower half of the crypt and sialomucins in the upper specificity and the intensity ofstaining with orcein was crypt (figs 3a and b); a reverse pattern was observed in similar to that seen in untreated sections stained with the right colon and the appendix. The above results orcein-alcian blue. J Clin Pathol: first published as 10.1136/jcp.42.8.881 on 1 August 1989. Downloaded from Orcein-alcian blue staining 883 F m f !aC .. ! 0 it' I ' copyright. Fig 3 Normal mucosa ofleft colon showingpredominance ofsulphatedmucin (brown) in lower crypt and sialomucin (blue) in the upper third ofcrypt: (a) orcein-alcian blue; (b) high iron diamine-alcian blue. Discussion this method, however, has yet to be investigated in other routine laboratories, and the lengthy staining Most research work carried out to study mucin time (more than 24 hours) and the relative complexity http://jcp.bmj.com/ secretion ofgastrointestinal epithelium has been based may deter laboratories from using it routinely. on only one technique-that is, the high iron diamine- Sipponen studied the distribution of cells positive alcian blue method.6 This stains sulphated mucins for orcein in the gastrointestinal tract and compared black and sialomucins blue. This technique has two the results with high iron diamine and AB 1-0 and 2-5.3 fundamental disadvantages, however: (i) The diamine With or without prior oxidation orcein, high iron reagents (N,N-dimethyl-m-phenylene-diamine and N, diamine and AB 1-0 gave similar results: it was N dimethyl-p-phenylenediamine) are carcinogenic concluded that, like high iron diamine or AB 1-0, the on September 28, 2021 by guest. Protected and hence require careful handling; (ii) it requires at orcein reactions stain sulphate groups in epithelial least an 18 hour staining period. The other drawbacks mucosubstances and that sulphonic acid residues, ofthis method are that some ofthe steps are crucial for resulting from the oxidation of sulphur groups (S-S or correct results. These include the commercial source of S-H) in the protein core of mucus glycoproteins were the reagents, the water rinse, pH of the solutions, responsible for the orcein, high iron diamine and concentration of the ferric chloride solution, and the alican blue reactions. The application ofthe dithionite use of freshly prepared diamine salts. Above all, the blocking technique, however, which gave an unchan- variations in staining method have also been reported ged orcein staining effect, meant that we were able to as giving different results.'4 show that orcein was stainipg sulphated mucin only in Recently, the KOH-AB1 0-PAPS method9 has been the material studied in spite of the oxidation step. used for detecting sulphated and sialomucins in the In this study we found that the intensity of orcein gastrointesinal epithelium and the results were com- staining was stronger with oxidation than without. pared with high iron diamine-alcian blue. It is claimed This can be explained by the fact that potassium that this technique is more sensitive in detecting cells permanganate oxidation enhances polyanionic reac- containing both types of mucins. Reproducibility of tions and also that orcein has a natural selective J Clin Pathol: first published as 10.1136/jcp.42.8.881 on 1 August 1989. Downloaded from 884 Singh, Gorton affinity for the sulphate moiety which is intensified only four hours for staining. It can therefore be after oxidation. Natural orcein also gave more stable routinely used as an aid to the diagnosis of pre- results than artificial orcein and that it could be malignant and malignant diseases of the gastrointes- combined with alican-blue.
Recommended publications
  • JB-4 Kit AGR1130
    Unit 7, M11 Business Link Parsonage Lane, Stansted Essex, UK CM24 8GF t: +44 (0)1279 813519 f: +44 (0)1279 815106 e: [email protected] w: www.agarscientific.com JB-4 Kit AGR1130 Introduction: JB-4 Embedding Kit is a unique polymer embedding material that gives a higher level of morphological detail than paraffin processed tissues. A water-soluble media, JB-4 does not require dehydration to absolute alcohol except for dense, bloody, or fatty tissue specimens. JB-4 is excellent for non-decalcified bone specimens, routine stains, special stains, and histochemical staining. Clearing agents such as xylene and chloroform are not required. The polymerization of JB-4 is exothermic, which is easily controlled by polymerizing on ice or by using refrigeration at 4°C. JB-4 Embedding Kits must be used under a chemical fume hood. Sections of JB-4 embedded material can be cut at 0.5 to 3.0 microns or thicker. Microtomes designed for plastic sectioning are required as are glass, Ralph, or tungsten carbide knives. Polysciences, Inc. has tungsten carbide knives available for most sectioning requirements. Sections can be stained for routine histological or histochemical procedures. Immunohistochemical procedures are not recommended for JB-4 as the glycol methacrylate cannot be removed from the section and may block antigen sites for most antibody reactions. As an alternative we recommend the Polysciences, Inc. Osteo-Bed Bone Embedding Kit. The Osteo-Bed formulation is a methyl methacrylate that is well suited for bone or for immunohistochemistry on routine histological specimens. NOTE: It is recommended that the Embedding Kit be used under a fume hood with appropriate gloves.
    [Show full text]
  • I. the Preparation and Morphology of a Quantified Urine Sediment
    Upsala J Med Sci 84: 67-74, 1979 The Effect of Short-term High-dose Treatment with Methenamine Hippurate of Urinary Infection in Geriatric Patients with Indwelling Catheters I. The preparation and morphology of a quantified urine sediment Bo Norberg, Astrid Norberg, Ulf Parkhede, Hans Gippert and MBns Akerman Departments of Internal Medicine, Pathology and Education, Univer.tity of Lund and the School of Nursing, Lund, Sweden. 3 A4 Riker Laboratories, Skurholmen, Swyden ABSTRACT A quantified sediment of the urine from patients with indwelling catheters was prepared by fixation of 0.1 ml urine in 0.9 ml 2% glutaraldehyde immediately after sampling. Slide preparations were then made from 0.2 ml of the glutaral- dehyde suspension by means of a cytocentrifuge. Bacteria and epithelial cells were properly contrasted by the May-Grunwald-Giemsa stain but haematoxylin- eosin and the Papanicolaou stain were superior as regards leukocyte morphology. It is suggested that glutaraldehyde-cytocentrifuge preparations of the urine cytology may be useful in the evaluation of urinary infection and in the evaluation of the therapy of urinary infection. INTRODUCTION The microscopic examination of urine sediments is a rapid and simple proce- dure which provides essential information in many cases of kidney disease or infections in the urinary tract. The conventional urinary sediment has, how- ever, serious pitfalls, e.g. low reproducibility, low precision and high vul- nerability to delay in transport and preparation (1-10). It nevertheless seemed desirable to make a quantified urine sediment from patients with indwelling catheters in order to evaluate urinary infection and the effects of therapy.
    [Show full text]
  • Mucin Histochemistry in Tumours of Colon, Ovaries and Lung
    ytology & f C H i o s l t a o n l o r g u y o Ali et al., J Cytol Histol 2012, 3:7 J Journal of Cytology & Histology DOI: 10.4172/2157-7099.1000163 ISSN: 2157-7099 ReviewResearch Article Article OpenOpen Access Access Mucin Histochemistry in Tumours of Colon, Ovaries and Lung Usman Ali*, Nagi AH, Nadia Naseem and Ehsan Ullah Department of Morbid Anatomy and Histopathology, University of Health Sciences, Lahore, Pakistan Abstract Introduction: Mucins implicated in cancers of various organs. The apical epithelial surfaces of mammalian respiratory, gastrointestinal, and reproductive tracts are coated by mucus, a mixture of water, ions, glycoproteins, proteins, and lipids. The purpose of this study was to confirm the presence of mucin production using Haematoxylin and Eosin (H&E) stain as the gold standard and to describe the types of mucins produced in tumors of lung, colon and ovaries using various types of histochemical techniques. Methods: The resection specimens and biopsies from tumours of colon (n=16), ovaries (n=13) and lung (n=5) were included and stained with H&E to determin the histological diagnosis for selecting tissues with mucin production. Slides were stained with PAS, Alcian blue, High iron diamine-Alcian blue, Meyer’s mucicarmine and Alcian blue-PAS to demonstrate the mucin production and to identify types of mucins. Results: In the present study we observed predominance of acid mucins over neutral mucins. In addition in these cases we observed sulphomucin predominating over sialomucin. Conclusion: Mucin histochemistry can effectively determine the types of mucins. Keywords: Haematoxylin and Eosin; Periodic acid schiff; High iron Materials and Methods diamine; Alcian blue Paraffin embedded sections were prepared using automatic tissue Introduction processor, followed by preparation of paraffin block using our embedding station.
    [Show full text]
  • T-Cell Brain Infiltration and Immature Antigen-Presenting Cells in Transgenic Models of Alzheimerв€™S Disease-Like Cerebral
    Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2016 T-cell brain infiltration and immature antigen-presenting cells in transgenic models of Alzheimer’s disease-like cerebral amyloidosis Ferretti, M T ; Merlini, M ; Späni, C ; Gericke, C ; Schweizer, N ; Enzmann, G ; Engelhardt, B ; Kulic, L ; Suter, T ; Nitsch, R M Abstract: Cerebral beta-amyloidosis, one of the pathological hallmarks of Alzheimer’s disease (AD), elicits a well-characterised, microglia-mediated local innate immune response. In contrast, it is not clear whether cells of the adaptive immune system, in particular T-cells, react to cerebral amyloidosis in AD. Even though parenchymal T-cells have been described in post-mortem brains of AD patients, it is not known whether infiltrating T-cells are specifically recruited to the extracellular deposits of beta-amyloid, and whether they are locally activated into proliferating, effector cells upon interaction with antigen- presenting cells (APCs). To address these issues we have analysed by confocal microscopy and flow- cytometry the localisation and activation status of both T-cells and APCs in transgenic (tg) mice models of AD-like cerebral amyloidosis. Increased numbers of infiltrating T-cells were found in amyloid-burdened brain regions of tg mice, with concomitant up-regulation of endothelial adhesion molecules ICAM-1 and VCAM-1, compared to non-tg littermates. The infiltrating T-cells in tg brains did not co-localise with amyloid plaques, produced less interferon-gamma than those in controls and did not proliferate locally. Bona-fide dendritic cells were virtually absent from the brain parenchyma of both non-tg andtgmice, and APCs from tg brains showed an immature phenotype, with accumulation of MHC-II in intracellular compartments.
    [Show full text]
  • Simple Technique to Identify Haemosiderin in Immunoperoxidase Stained Sections
    J Clin Pathol: first published as 10.1136/jcp.37.10.1190 on 1 October 1984. Downloaded from 1190 Technical methods Phosphate buffer at pH 8*0 gave the sharpest 2 Rozenszajn L, Leibovich M, Shoham D, Epstein J. The esterase staining reactions, although there was little differ- activity in megaloblasts, leukaemic and normal haemopoietic cells. Br J Haematol 1968; 14:605-19. ence at pH 7-0 or pH 7-5. As the buffer pH was 3Hayhoe FGJ, Quaglino D. Haematological cytochemistry. Edin- increased above pH 8-0 staining with both substrates burgh: Churchill Livingstone, 1980. became progressively weaker, especially above pH 4Li CY, Lam KW, Yam LT. Esterases in human leucocytes. J 9.0. Below pH 7-0 staining with a-naphthyl butyrate Histochem Cytochem 1973;21:1-12. Yam LT, Li CY, Crosby WH. Cytochemical identification of became weaker, and below pH 5*0 staining with monocytes and granulocytes. Am J Clin Pathol 1971;55:283- naphthol AS-D chloroacetate began to disappear. 90. 6 Armitage RJ, Linch DC, Worman CP, Cawley JC. The morphol- This work was supported by a Medical Research ogy and cytochemistry of human T-cell subpopulations defined by monoclonal antibodies and Fc receptors. Br J Haematol Council project grant. I thank Professor FGJ 1983;51:605-13. Hayhoe for valuable advice. References Requests for reprints to: Dr DM Swirsky, Department of Gomori G. Chloroacyl esters as histochemical substrates. J His- Haematological Medicine, University Clinical School, Hills tochem Cytochem 1953;1:469-70. Road, Cambridge CB2 2QL, England. Simple technique to identify identification of the two compounds on the same haemosiderin in slide.
    [Show full text]
  • New Tetrachromic VOF Stain (Type III-G.S) for Normal and Pathological Fish Tissues C
    ORIGINAL PAPER New Tetrachromic VOF Stain (Type III-G.S) for Normal and Pathological Fish Tissues C. Sarasquete,* M. Gutiérrez Instituto de Ciencias Marinas de Andalucía, CSIC Polígono Río San Pedro, Apdo oficial, Puerto Real, Cádiz, Spain richrome methods invariably use dyes in acid ©2005, European Journal of Histochemistry pH solvents, usually diluted in aqueous acetic Tacid, and the concentration of this acid A new VOF Type III-G.S stain was applied to histological sec- matches the concentration of dye. Staining depends tions of different organs and tissues of healthy and pathologi- largely on the attachment of dyes to proteins. The cal larvae, juvenile and adult fish species (Solea senegalensis; acid pH itself is necessary to maximise the amount Sparus aurata; Diplodus sargo; Pagrus auriga; Argyrosomus regius and Halobatrachus didactylus). In comparison to the of dye that will attach to tissue amino groups. original Gutiérrez´VOF stain, more acid dyes of contrasting Proteins have both positively (amino groups) and colours and polychromatic/metachromatic properties were negatively (carboxyl and hydroxyl) charged groups. incorporated as essential constituents of the tetrachromic VOF Usually one predominates and this will have an stain. This facilitates the selective staining of different basic tissues and improves the morphological analysis of histo- overall negative or positive charge (being an acid or chemical approaches of the cell components. The VOF-Type III a basic protein). These charges can, however, bal- G.S stain is composed of a mixture of several dyes of varying ance each other out to some degree. Phosphate size and molecular weight (Orange G< acid Fuchsin< Light green<Methyl Blue<Fast Green), which are used simultane- groups of DNA and binding-proteins are important ously, and it enables the individual tissues to be selectively dif- in nuclear staining.The ionisation of basic groups of ferentiated and stained.
    [Show full text]
  • Hito Oil Red O Optimstain™ Kit Manual and MSDS
    Simple Solution for Your Research Hito Oil Red O OptimStain™ Kit [Catalog Number: HTKLS0122] An easy to use Oil Red O staining system for the lipid and fat staining on frozen sections User Manual And Material Safety Data Sheet FOR IN VITRO RESEARCH USE ONLY Hitobiotec Corp. Simple solution for your research Hito Oil Red O OptimStain™ Kit [Catalog Number: HTKLS0122] An easy to use Oil Red O staining system for the lipid and fat staining on frozen sections User Manual And Material Safety Data Sheet FOR IN VITRO RESEARCH USE ONLY Hitobiotec Corp. © 2017 All Rights Reserved Index I. Introduction 2 II. Kit Contents 3 III. Tissue Preparation 4 IV. Staining Procedure 8 V. References 11 VI. Material Safety Data Sheet (MSDS) 12 1 I. Introduction Hito Oil Red O OptimStain™ Kit is designed based on the Oil Red O staining method. Oil Red O is a common staining technique for studying the morphology of lipids in adipose tissue. It allows localization and visualization of the lipids in the aortic sinus and aorta to determine the extent of atherosclerosis, and remains as one of the primary techniques for visualization of the atherosclerosis pattern at the aortic sinus. Accordingly, Oil Red O staining techniques are not only useful for tissue histology studies, but also widely used in cell biological studies examining intracellular lipid metabolism 1-5. Hito Oil Red O OptimStain™ Kit makes further improve- ment over the Oil Red O method and simplifies the staining technique. It offers high quality, rapid, reliable and easy to use staining of the lipids and fat.
    [Show full text]
  • Preclinical Studies of the First in Human Sarna Drug Candidate for Liver Cancer
    Oncogene (2018) 37:3216–3228 https://doi.org/10.1038/s41388-018-0126-2 ARTICLE Gene activation of CEBPA using saRNA: preclinical studies of the first in human saRNA drug candidate for liver cancer 1 2 2 3 4 1 Vikash Reebye ● Kai-Wen Huang ● Vivian Lin ● Sheba Jarvis ● Pedro Cutilas ● Stephanie Dorman ● 5 1 5 6,7 1 1 Simona Ciriello ● Pinelopi Andrikakou ● Jon Voutila ● Pal Saetrom ● Paul J. Mintz ● Isabella Reccia ● 8 9 5 10 5 1 John J. Rossi ● Hans Huber ● Robert Habib ● Nikos Kostomitsopoulos ● David C. Blakey ● Nagy A. Habib Received: 2 July 2017 / Revised: 2 December 2017 / Accepted: 12 December 2017 / Published online: 7 March 2018 © The Author(s) 2018. This article is published with open access Abstract Liver diseases are a growing epidemic worldwide. If unresolved, liver fibrosis develops and can lead to cirrhosis and clinical decompensation. Around 5% of cirrhotic liver diseased patients develop hepatocellular carcinoma (HCC), which in its advanced stages has limited therapeutic options and negative survival outcomes. CEPBA is a master regulator of hepatic function where its expression is known to be suppressed in many forms of liver disease including HCC. Injection of MTL-CEBPA, a small activating RNA oligonucleotide therapy (CEBPA-51) formulated in liposomal nanoparticles 1234567890();,: 1234567890();,: (NOV340- SMARTICLES) upregulates hepatic CEBPA expression. Here we show how MTL-CEBPA therapy promotes disease reversal in rodent models of cirrhosis, fibrosis, hepatosteatosis, and significantly reduces tumor burden in cirrhotic HCC. Restoration of liver function markers were observed in a carbon-tetrachloride-induced rat model of fibrosis following 2 weeks of MTL-CEBPA therapy.
    [Show full text]
  • Haematoxylin and Eosin in Histology
    Two hand in hand lovers on a glassy path: haematoxylin and eosin in histology Raffaella Santi, MD PhD Careggi University Hospital, Florence, Italy Paraffin-embedded tissue sections are routinely stained with H&E nowadays. Only when clinical history, gross examination or H&E study suggests it are other “special” stains employed to delineate better features poorly or not all brought out by H&E Staining is such an integral part of modern histology that it is difficult to think of being without it. H&E have become the inimitable scaffold on which many diagnoses are made every day HAEMATOXYLIN & EOSIN HAEMATOXYLIN Haematoxylum Campechianum (Logwood ) Titford M, 2005 In the early 16th century when the Spanish explored the coast of the Yucatan Peninsula in search of gold and silver, they found logwood and they introduced it to European textile makers as a competitor to indigo. Logwood soon became a target of piracy, with English, French and Dutch forces all seeking to profit from its use. Its value was such that Spain initially claimed a monopoly on all logwood sales and later, the right to profit from logwood plantations, was part of the political statement that followed the Seven Years’ War (1756-1763) between Britain, France and Spain Treaty of Paris (1763) The earliest recorded European settlers to Belize were shipwrecked British sailors, otherwise known as the “Baymen” who first arrived in 1638. The Baymen became loggers, sending tons of logwood back to England throughout 1700 and 1800s Such was their notoriety that the national flag and currency of Belize depict the Baymen still today Haematoxylin was mainly used as a fabric dye and stained the uniforms of soldiers in the American Civil War (1861-65) and subsequently in the First and the Second World Wars.
    [Show full text]
  • Utilization of 1% of Methylene Blue in Staining Histopathological Preparations at Anatomic Pathology Laboratory
    Utilization of 1% of Methylene Blue in Staining Histopathological Preparations at Anatomic Pathology Laboratory Tri Rahmawati1, Yadi Apriyadi2, Mamay1 1Department of Medical Laboratory Abstract Technology, STIKes Karsa Husada, Tissue staining using hematoxylin-eosin (HE) is a standard Garut, Indonesia method of histopathological staining. The tissue staining 2Departement Pathology of is hampered when there is no hematoxylin reagent in Anatomi, Regional public hospital laboratory. Therefore, other reagents are needed that can Dr. Slamet, Garut, Indonesia replace the use of hematoxylin. Methylene blue is a basic Correspondence: dyes that interact with cell nuclei which has a negative ionic Mamay, charge of the tissue. It can be used as an alternative nuclei Jl. Nusa Indah No.1, Jayaraga, Kec. staining. This study aims to evaluate the use of 1% of Tarogong Kidul, Kabupaten Garut methylene blue in cell nuclei staining in histopathological Zip Code : 44151 preparations. The research sample were 15 pathology preparations which were randomly selected including breast Email: [email protected] cancer, cervical cancer and ovarian cancer in the bank of sampel at anatomical pathology laboratory of RSUD Dr. Received: May 31, 2020 Slamet Garut, Indonesia. The experiment showed that the Revised: June 19, 2020 methylene blue dyes yielded “worth” result (40%) and Accepted: August 25, 2020 “poorly” result (60%). Further research can be carried out by modifying the pH of 1% of methylene blue reagent so that it can maximize the staining preparations results as good as those using hematoxylin. Keywords Cancer, hematoxylin, histopathology, methylene blue INTRODUCTION prevalence of tumors or cancer in Indonesia Cancer prevalence is increasing in the shows an increase from 1.4 per thousand world every year.
    [Show full text]
  • Mayer's Hematoxylin Solution
    MAYER’S 6. Filter working stain solution daily. Rotate alcohols and xylene/xylene substitute daily. HEMATOXYLIN SOLUTION 7. Adding new stock to depleted working solutions of Mayer’s Hema tox y lin or Eosin is (Procedure No. MHS) not recommended. _______________________________________________ 8. Avoid excessive water carry-over into Mayer’s Hematoxylin. 9. Positive control slides should be included in each run. INTENDED USE 10. The data obtained from this procedure serves only as an aid to diagnosis and should be _______________________________________________ reviewed in conjunction with other clinical diagnostic tests or information. Mayer’s Hematoxylin Solution is commonly used after immu no his tochem is try or PROCEDURE 1: cytochemistry staining as a nuclear counterstain. It may also be used for standard hematoxylin HEMATOXYLIN AND EOSIN STAINING and eosin (H&E) staining, but it is more com mon ly used where acid alcohol differentiation, or 3 1. Prepare a 95% alcohol solution by adding 5 ml deionized water to 95 ml Reagent exposure to alcohol, might destroy the stained cytoplasmic component. Mayer’s Hematoxylin Solution is for mu lat ed without alcohol, and as such will not dissolve out AEC (3-amino-9- Alcohol or Ethanol (100%). ethylcarbazole), alkaline phosphatase/Fast Red chromogen or other soluble colored products. 2. Deparafnize to water or fix and hydrate frozen sections. Mayer’s Hematoxylin Solutions are for “In Vitro Diagnostic Use”. 3. Stain in Mayer’s Hematoxylin Solution...................................................................15 minutes Hematoxylin, a common nuclear stain, is isolated from an extract of logwood (Haematoxylin 4. Rinse in warm running tap water............................................................................15 minutes campechianun).1 The first successful bi o log ic ap pli ca tion of hematoxylin was described by 5.
    [Show full text]
  • Histochemical Studies of the Extracellular Matrix of Human Articular Cartilage—A Review J
    Osteoarthritis and Cartilage (2002) 10, 333–343 © 2002 OsteoArthritis Research Society International. Published by Elsevier Science Ltd. All rights reserved. 1063–4584/02/$35.00/0 doi:10.1053/joca.2002.0519, available online at http://www.idealibrary.com on Histochemical studies of the extracellular matrix of human articular cartilage—a review J. L. Hyllested, K. Veje and K. Ostergaard Osteoarthritis Research Unit, Institute for Inflammation Research (IIR), 7521 Finsencentre, National University Hospital, Rigshospitalet, Copenhagen, Denmark Summary Objective: This paper reviews the histochemistry of the extracellular matrix of human articular cartilage. No systematic review of histochemical knowledge and techniques in the study of articular cartilage has been published previously. Methods and results: Literature was searched in the Winspirs Medline database from 1960 to 2000. Only techniques applicable for bright field or polarization microscopy were considered. Unless otherwise noted, all applies to hyaline cartilage. The most widely used fixatives are adequate for routine staining of proteins, but proteoglycan fixation is problematic, and no one fixative can be recommended. Proteoglycan can be stained reliably but it is problematic that, at low substrate concentrations, these methods are not stoichiometric. Collagen can be stained efficiently, although attempts to differentiate collagen types have not been successful. Conclusions: Detailed studies of fixation and staining procedures should be carried out and standards for cartilage sampling, handling and evaluation agreed upon if results from different laboratories are to be compared. © 2002 OsteoArthritis Research Society International. Published by Elsevier Science Ltd. All rights reserved. Key words: Human cartilage, Histochemistry, Fixation, Staining. Introduction avascular matrix composed of water (70% wet w/w)7, proteoglycans8, collagens (50–90% dry w/w)9 and non- Human articular cartilage is the site of osteoarthritis (OA), collagenous proteins10.
    [Show full text]