Basic Biology of the Skin 3
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Diapositiva 1
Ingegneria delle tecnologie per la salute Fondamenti di anatomia e istologia Apparato tegumentario aa. 2017-18 INTEGUMENTARY SYSTEM integumentary system = refers to skin and its accessory structures responsible for much more than simply human outward appearance: about 16% of body weight, covering an area of 1.5 to 2 m2 (= largest organ system in human body). • skin protects inner organs INTEGUMENTARY SYSTEM • skin = even not typical, but an organ, made of tissues that work together as a single structure to perform unique and critical functions • integumentary system = skin + its accessory structures, providing body with overall protection. • made of multiple layers of cells and tissues, which are held to underlying structures by connective tissue: deeper layer of skin is well vascularized (has numerous blood vessels) and also has numerous sensory, and autonomic and sympathetic nerve fibers ensuring communication to and from brain. INTEGUMENTARY SYSTEM Overview • Largest organ (15% of body weight) • Epidermis – keratinized stratified squamous epithelium • Dermis – connective tissue layer • Hypodermis • Thickness variable, normally 1-2 mm – dermis may thicken, up to 6 mm – stratum corneum layer increased • calluses on hands and feet Structure of the Skin 2 layers: epidermis + dermis SKIN: histology SKIN: histology SKIN: histology Cells of the Epidermis • Stem cells – undifferentiated cells in deepest layers • Keratinocytes – most of the skin cells • Melanocytes – synthesize pigment that shield UV • Tactile (merkel) cells – receptor cells associated with nerve fibers • Dendritic (langerhans) cells – macrophages guard against pathogens Cell and Layers of the Epidermis Epidermis: histology = composed of keratinized, stratified squamous epithelium, made of 4 or 5 layers of epithelial cells, depending on its location in body. -
Tbwhat You Need to Know About the Tuberculosis Skin Test
What You Need to Know About TB the Tuberculosis Skin Test “I was told I needed a TB skin test, so I went to the health clinic. It was quick and didn’t hurt. In two days, I went back to the clinic so the nurse could see the results. It’s important to go back in 2 or 3 days to get your results or you will have to get the test again.” A TB skin test will tell you if you have ever had TB germs in your body. • A harmless fluid is placed under your skin on the inside of your arm. A very small needle is used, so you will only feel a light pinch. • Make sure you don’t put a bandage or lotion on the test spot. Also—don’t scratch the spot. If the area itches, put an ice cube or cold cloth on it. It is okay for the test spot to get wet, but do not wipe or scrub the area. • Return to the clinic or doctor’s office in 2 to 3 days so your healthcare provider can look at the test spot on your arm. He or she will look at the test spot and measure any bump that appears there. Your healthcare provider will let you know if your test is negative or positive. Write the time and date you will need to return here: 2 Remember—only a healthcare provider can read your TB skin test results the right way. When your skin test is positive: • You have TB germs in your body. -
Nail Anatomy and Physiology for the Clinician 1
Nail Anatomy and Physiology for the Clinician 1 The nails have several important uses, which are as they are produced and remain stored during easily appreciable when the nails are absent or growth. they lose their function. The most evident use of It is therefore important to know how the fi ngernails is to be an ornament of the hand, but healthy nail appears and how it is formed, in we must not underestimate other important func- order to detect signs of pathology and understand tions, such as the protective value of the nail plate their pathogenesis. against trauma to the underlying distal phalanx, its counterpressure effect to the pulp important for walking and for tactile sensation, the scratch- 1.1 Nail Anatomy ing function, and the importance of fi ngernails and Physiology for manipulation of small objects. The nails can also provide information about What we call “nail” is the nail plate, the fi nal part the person’s work, habits, and health status, as of the activity of 4 epithelia that proliferate and several well-known nail features are a clue to sys- differentiate in a specifi c manner, in order to form temic diseases. Abnormal nails due to biting or and protect a healthy nail plate [1 ]. The “nail onychotillomania give clues to the person’s emo- unit” (Fig. 1.1 ) is composed by: tional/psychiatric status. Nail samples are uti- • Nail matrix: responsible for nail plate production lized for forensic and toxicology analysis, as • Nail folds: responsible for protection of the several substances are deposited in the nail plate nail matrix Proximal nail fold Nail plate Fig. -
Wound Classification
Wound Classification Presented by Dr. Karen Zulkowski, D.N.S., RN Montana State University Welcome! Thank you for joining this webinar about how to assess and measure a wound. 2 A Little About Myself… • Associate professor at Montana State University • Executive editor of the Journal of the World Council of Enterstomal Therapists (JWCET) and WCET International Ostomy Guidelines (2014) • Editorial board member of Ostomy Wound Management and Advances in Skin and Wound Care • Legal consultant • Former NPUAP board member 3 Today We Will Talk About • How to assess a wound • How to measure a wound Please make a note of your questions. Your Quality Improvement (QI) Specialists will follow up with you after this webinar to address them. 4 Assessing and Measuring Wounds • You completed a skin assessment and found a wound. • Now you need to determine what type of wound you found. • If it is a pressure ulcer, you need to determine the stage. 5 Assessing and Measuring Wounds This is important because— • Each type of wound has a different etiology. • Treatment may be very different. However— • Not all wounds are clear cut. • The cause may be multifactoral. 6 Types of Wounds • Vascular (arterial, venous, and mixed) • Neuropathic (diabetic) • Moisture-associated dermatitis • Skin tear • Pressure ulcer 7 Mixed Etiologies Many wounds have mixed etiologies. • There may be both venous and arterial insufficiency. • There may be diabetes and pressure characteristics. 8 Moisture-Associated Skin Damage • Also called perineal dermatitis, diaper rash, incontinence-associated dermatitis (often confused with pressure ulcers) • An inflammation of the skin in the perineal area, on and between the buttocks, into the skin folds, and down the inner thighs • Scaling of the skin with papule and vesicle formation: – These may open, with “weeping” of the skin, which exacerbates skin damage. -
The Distribution of Sweat Glands Over the Human Body Has So Far Been In
NOTES ON THE VERTICAL DISTRIBUTION OF THE HUMAN SWEAT GLANDS SHUNZO TAKAGI AND KO TOBARU* Institute of Physiology, School of Medicine, University of Nagoya•õ The distribution of sweat glands over the human body has so far been in- vestigated in the dimension of area, and we have no general idea how deep they are distributed in the skin. In 1943, Kuno and his collaborators (3) expressed the opinion that chloride would be accumulated in the skin during the activity of sweat glands. The truth of this assumption has been confirmed with more certainty by Yoshimura and Chihaya (unpublished), who measured the chloride content in the skin tissue by means of Ag-AgCl electrodes. The chloride may presumably be accumulated in the immediate neighbourhood of the glomeruli of sweat glands, or more diffusely in the layers of skin tissues where the glomeruli are situated. For consideration of the amount of the accumulated chloride, the total volume of these skin layers, which can be estimated by the vertical distribution of the sweat-gland glomeruli, seems to be useful. The fol- lowing investigation was therefore performed. MATERIALS AND METHOD Skin samples of 33 regions of the body, as specified in table 1, were taken from the corpse of a Japanese male of 30 years old, who died an accidental death. The samples were fixed in 10 per cent formalin, embedded in celloidin and cut into sections 15 micra thick. The sections were stained with Delafield's hematoxylin and eosin. Observations of sweat glands were made with 2-3 pieces of the skin about 100 sq. -
Touch and Temperature Senses
1 In press in Proceedings of the Association for Biology Laboratory Education (ABLE), 2004 Touch and Temperature Senses by Charlie Drewes Ecology, Evolution & Organismal Biology Iowa State University Ames, IA 50011 (515) 294-8061 [email protected] http://www.eeob.iastate.edu/faculty/DrewesC/htdocs/ Biographical: Charlie Drewes received a BA in biology from Augustana College (SD) and his MS and PhD in zoology from Michigan State University. Currently, he is a professor in Ecology, Evolution and Organismal Biology at Iowa State University. His research focus is on rapid escape reflexes and locomotion, especially in oligochaete worms. Charlie teaches courses in invertebrate biology, neurobiology and bioethics. During summers, he leads hands-on, residential workshops for high school biology teachers at Iowa Lakeside Lab. In 1998, he received the Distinguished Science Teaching Award from the Iowa Academy of Science and, in 2002, he received the Four-year College Biology Teaching Award from the National Association of Biology Teachers. Abstract: This investigation focuses on the sensory biology of human touch and temperature reception. Students investigate quantitative and qualitative aspects of touch-sensory functions in human skin. Values for two-point discrimination are compared to Weber’s original data. Also, novel materials and methods are introduced for investigating the functional organization of cold sensory reception in human skin, including: (a) estimation of sensory field size for single cold-sensory fibers, (b) demonstration of the discontinuous distribution of cold-sensory fibers in skin, and (c) estimation of the density of cold-sensitive fibers per unit area of skin. Tactile and thermoreceptor functions are related to underlying neuroanatomy of peripheral and central neural pathways. -
A Spectral BSSRDF for Shading Human Skin
Eurographics Symposium on Rendering (2006) Tomas Akenine-Möller and Wolfgang Heidrich (Editors) A Spectral BSSRDF for Shading Human Skin Craig Donner and Henrik Wann Jensen† Universtiy of California at San Diego, La Jolla, CA, USA Abstract We present a novel spectral shading model for human skin. Our model accounts for both subsurface and surface scattering, and uses only four parameters to simulate the interaction of light with human skin. The four parameters control the amount of oil, melanin and hemoglobin in the skin, which makes it possible to match specific skin types. Using these parameters we generate custom wavelength dependent diffusion profiles for a two-layer skin model that account for subsurface scattering within the skin. These diffusion profiles are computed using convolved diffusion multipoles, enabling an accurate and rapid simulation of the subsurface scattering of light within skin. We combine the subsurface scattering simulation with a Torrance-Sparrow BRDF model to simulate the interaction of light with an oily layer at the surface of the skin. Our results demonstrate that this four parameter model makes it possible to simulate the range of natural appearance of human skin including African, Asian, and Caucasian skin types. Categories and Subject Descriptors (according to ACM CCS): I.3.7 [Computer Graphics]: Color, shading, shadowing, and texture 1 Introduction Debevec et al. [DHT∗00] measured the reflectance field of human faces, allowing for rendering of skin under varying Simulating the appearance of human skin is a challenging illumination conditions with excellent results. Jensen and problem due to the complex structure of the skin. Further- Buhler [JB02], Hery [Her03] and Weyrich et al. -
Isolation and Growth of Adult Human Epidermal Keratinocytes in Cell Culture
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector CITATION CLASSIC 0022-202X/78/7102-0157$02.00/0 THE JOURNAL OF INVESTIGATIVE DERMATOLOGY, 71:157–162, 1978 Vol. 71, No. 2 Copyright & 1978 by The Williams & Wilkins Co. PrintedinU.S.A. Isolation and Growth of Adult Human Epidermal Keratinocytes in Cell Culture SU-CHIN LIU,PH.D., AND MARVIN KARASEK,PH.D. Humanepidermalkeratinocytesmaybeisolatedinhighyieldfrom 0.1 mm keratotome sections of adult skin by short-term trypsinrelease.Whenplatedonacollagen-coatedplasticsurfaceor on a collagen gel, keratinocytes attach with high efficiencies (470%) and form confluent, stratified cultures. Cell populations of predominantly basal cells produce proliferative primary cell cultures while populations of basal cells and malpighian cells result in nonproliferative primary cultures. Both nonproliferative and proliferative primary cultures may be subcultured on collagen gels following dispersion by trypsin and EDTA. Methotrexate strongly inhibits proliferative keratinocytes at low concentrations (0.1 mg/ml) but has no cytotoxic effect on non- proliferative cells. L-serine and dexamethasone increase the multiplication rate of both primary and subcultured human keratinocytes. The ability to isolate and to grow human epidermal keratinocytes from Preparation of Collagen Surfaces both normal and diseased human skin in sufficient quantities for Acid soluble collagen is extracted and purified from adult rabbit skin as described biochemical and genetic studies has been a long-range goal of many previously [10]. Three types of culture surfaces are prepared on 35-mm plastic investigators. Although keratinocytes may be obtained from postem- Petri dishes: (a) collagen-coated, (b) thin gel, and (c) 2-mm collagen gel. -
Enabling Sweat-Based Biosensors: Solving the Problem of Low
Enabling sweat-based biosensors: Solving the problem of low biomarker concentration in sweat A dissertation submitted to the Graduate School of the University of Cincinnati in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Biomedical Engineering of the College of Engineering & Applied Science by Andrew J. Jajack B.S., Biology, Wittenberg University, 2014 Committee Chairs: Jason C. Heikenfeld, Ph.D. and Chia-Ying Lin, Ph.D. Abstract Non-invasive, sweat biosensing will enable the development of an entirely new class of wearable devices capable of assessing health on a minute-to-minute basis. Every aspect of healthcare stands to benefit: prevention (activity tracking, stress-level monitoring, over-exertion alerting, dehydration warning), diagnosis (early-detection, new diagnostic techniques), and management (glucose tracking, drug-dose monitoring). Currently, blood is the gold standard for measuring the level of most biomarkers in the body. Unlike blood, sweat can be measured outside of the body with little inconvenience. While some biomarkers are produced in the sweat gland itself, most are produced elsewhere and must diffuse into sweat. These biomarkers come directly from blood or interstitial fluid which surrounds the sweat gland. However, a two-cell thick epithelium acts as barrier and dilutes most biomarkers in sweat. As a result, many biomarkers that would be useful to monitor are diluted in sweat to concentrations below what can be detected by current biosensors. This is a core challenge that must be overcome before the advantages of sweat biosensing can be fully realized. The objective of this dissertation is to develop methods of concentrating biomarkers in sweat to bring them into range of available biosensors. -
Pressure Ulcer Staging Guide
Pressure Ulcer Staging Guide Pressure Ulcer Staging Guide STAGE I STAGE IV Intact skin with non-blanchable Full thickness tissue loss with exposed redness of a localized area usually Reddened area bone, tendon, or muscle. Slough or eschar may be present on some parts Epidermis over a bony prominence. Darkly Epidermis pigmented skin may not have of the wound bed. Often includes undermining and tunneling. The depth visible blanching; its color may Dermis of a stage IV pressure ulcer varies by Dermis differ from the surrounding area. anatomical location. The bridge of the This area may be painful, firm, soft, nose, ear, occiput, and malleolus do not warmer, or cooler as compared to have subcutaneous tissue and these adjacent tissue. Stage I may be Adipose tissue ulcers can be shallow. Stage IV ulcers Adipose tissue difficult to detect in individuals with can extend into muscle and/or Muscle dark skin tones. May indicate "at supporting structures (e.g., fascia, Muscle risk" persons (a heralding sign of Bone tendon, or joint capsule) making risk). osteomyelitis possible. Exposed bone/ Bone tendon is visible or directly palpable. STAGE II DEEP TISSUE INJURY Partial thickness loss of dermis Blister Purple or maroon localized area of Reddened area presenting as a shallow open ulcer discolored intact skin or blood-filled Epidermis with a red pink wound bed, without Epidermis blister due to damage of underlying soft slough. May also present as an tissue from pressure and/or shear. The intact or open/ruptured serum-filled Dermis area may be preceded by tissue that is Dermis blister. -
Nomina Histologica Veterinaria, First Edition
NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria. -
Sweat Glands • Oil Glands • Mammary Glands
Chapter 4 The Integumentary System Lecture Presentation by Steven Bassett Southeast Community College © 2015 Pearson Education, Inc. Introduction • The integumentary system is composed of: • Skin • Hair • Nails • Sweat glands • Oil glands • Mammary glands © 2015 Pearson Education, Inc. Introduction • The skin is the most visible organ of the body • Clinicians can tell a lot about the overall health of the body by examining the skin • Skin helps protect from the environment • Skin helps to regulate body temperature © 2015 Pearson Education, Inc. Integumentary Structure and Function • Cutaneous Membrane • Epidermis • Dermis • Accessory Structures • Hair follicles • Exocrine glands • Nails © 2015 Pearson Education, Inc. Figure 4.1 Functional Organization of the Integumentary System Integumentary System FUNCTIONS • Physical protection from • Synthesis and storage • Coordination of immune • Sensory information • Excretion environmental hazards of lipid reserves response to pathogens • Synthesis of vitamin D3 • Thermoregulation and cancers in skin Cutaneous Membrane Accessory Structures Epidermis Dermis Hair Follicles Exocrine Glands Nails • Protects dermis from Papillary Layer Reticular Layer • Produce hairs that • Assist in • Protect and trauma, chemicals protect skull thermoregulation support tips • Nourishes and • Restricts spread of • Controls skin permeability, • Produce hairs that • Excrete wastes of fingers and supports pathogens prevents water loss provide delicate • Lubricate toes epidermis penetrating epidermis • Prevents entry of