Epidermis (Ectoderm), Dermis (Mesoderm), Subcutaneous Fat and Skin Appendages (Ectoderm and Mesoderm)
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Mechanical Stretch on Human Skin Equivalents Increases the Epidermal Thickness and Develops the Basement Membrane
RESEARCH ARTICLE Mechanical Stretch on Human Skin Equivalents Increases the Epidermal Thickness and Develops the Basement Membrane Eijiro Tokuyama1*, Yusuke Nagai2, Ken Takahashi3, Yoshihiro Kimata1, Keiji Naruse3 1 The Department of Plastic and Reconstructive Surgery, Okayama University Graduate School of Medicine, Okayama, Japan, 2 Menicon Co., Ltd., Aichi, Japan, 3 The Department of Cardiovascular Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan * [email protected] Abstract OPEN ACCESS Citation: Tokuyama E, Nagai Y, Takahashi K, Kimata All previous reports concerning the effect of stretch on cultured skin cells dealt with experi- Y, Naruse K (2015) Mechanical Stretch on Human ments on epidermal keratinocytes or dermal fibroblasts alone. The aim of the present study Skin Equivalents Increases the Epidermal Thickness was to develop a system that allows application of stretch stimuli to human skin equivalents and Develops the Basement Membrane. PLoS ONE 10(11): e0141989. doi:10.1371/journal.pone.0141989 (HSEs), prepared by coculturing of these two types of cells. In addition, this study aimed to analyze the effect of a stretch on keratinization of the epidermis and on the basement mem- Editor: Christophe Egles, Université de Technologie de Compiègne, FRANCE brane. HSEs were prepared in a gutter-like structure created with a porous silicone sheet in a silicone chamber. After 5-day stimulation with stretching, HSEs were analyzed histologi- Received: April 18, 2015 cally and immunohistologically. Stretch-stimulated HSEs had a thicker epidermal layer and Accepted: October 15, 2015 expressed significantly greater levels of laminin 5 and collagen IV/VII in the basal layer com- Published: November 3, 2015 pared with HSEs not subjected to stretch stimulation. -
A Practical Technique for Differentiation of Subepidermal Bullous Diseases Localization of in Vivo–Bound Igg by Laser Scanning Confocal Microscopy
STUDY A Practical Technique for Differentiation of Subepidermal Bullous Diseases Localization of In Vivo–Bound IgG by Laser Scanning Confocal Microscopy Katarzyna Woz´niak, MD; Takashi Kazama, MD; Cezary Kowalewski, MD Objective: To develop a practical technique to distin- whereas basement membrane zone markers were la- guish autoimmune subepidermal bullous diseases. beled with anti–mouse Cy5-conjugated antibodies. Design: A prospective study. Results: In patients with bullous pemphigoid, in vivo– bound IgG was localized on the epidermal side of lami-  Setting: Academic referral center—the Department of nin 5 and co-localized with 4 integrin. In patients with Dermatology, Medical University of Warsaw. mucous membrane pemphigoid, IgG was in vivo bound to the dermal-epidermal junction between localization Patients: Forty-two patients fulfilling clinical, immu- of laminin 5 and type IV collagen. In patients with epi- nological, and/or immunoelectron microscopic criteria dermolysis bullosa acquisita, in vivo–bound IgG was for bullous pemphigoid (n=31), mucous membrane pem- present on the dermal side of type IV collagen. phigoid (n=6), or epidermolysis bullosa acquisita (n=5), diagnosed as having disease and treated from January 1, Conclusions: Laser scanning confocal microscopy al- 1997, to December 31, 2002. lows precise localization of in vivo–bound IgG in pa- tients’ skin and, thus, it is a rapid method for the differ- Main Outcome Measures: We applied laser scan- entiation of mucous membrane pemphigoid from bullous ning confocal microscopy to determine the localization pemphigoid and epidermolysis bullosa acquisita. This tool of in vivo–bound IgG at the basement membrane zone is suitable for the routine diagnosis of individual pa- in biopsy specimens taken from patients’ skin to com- tients and for retrospective studies. -
Corrective Gene Transfer of Keratinocytes from Patients with Junctional Epidermolysis Bullosa Restores Assembly of Hemidesmosomes in Reconstructed Epithelia
Gene Therapy (1998) 5, 1322–1332 1998 Stockton Press All rights reserved 0969-7128/98 $12.00 http://www.stockton-press.co.uk/gt Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia J Vailly1, L Gagnoux-Palacios1, E Dell’Ambra2, C Rome´ro1, M Pinola3, G Zambruno3, M De Luca2,3 J-P Ortonne1,4 and G Meneguzzi1 1U385 INSERM, Faculte´ de Me´decine, Nice; 4Service de Dermatologie, Hoˆpital L’Archet, Nice, France; Laboratories of 2Tissue Engineering and 3Molecular and Cell Biology, Istituto Dermopatico dell’Immacolata, Rome, Italy Herlitz junctional epidermolysis bullosa (H-JEB) provides deposited into the extracellular matrix. Re-expression of a promising model for somatic gene therapy of heritable laminin-5 induced cell spreading, nucleation of hemides- mechano-bullous disorders. This genodermatosis is mosomal-like structures and enhanced adhesion to the cul- caused by the lack of laminin-5 that results in absence of ture substrate. Organotypic cultures performed with the hemidesmosomes (HD) and defective adhesion of squam- transduced keratinocytes, reconstituted epidermis closely ous epithelia. To establish whether re-expression of lami- adhering to the mesenchyme and presenting mature hemi- nin-5 can restore assembly of the dermal-epidermal attach- desmosomes, bridging the cytoplasmic intermediate fila- ment structures lacking in the H-JEB skin, we corrected the ments of the basal cells to the anchoring filaments of the genetic mutation hindering expression of the 3 chain of basement membrane. Our results provide the first evi- laminin-5 in human H-JEB keratinocytes by transfer of a dence of phenotypic reversion of JEB keratinocytes by laminin 3 transgene. -
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. -
Adherens Junctions, Desmosomes and Tight Junctions in Epidermal Barrier Function Johanna M
14 The Open Dermatology Journal, 2010, 4, 14-20 Open Access Adherens Junctions, Desmosomes and Tight Junctions in Epidermal Barrier Function Johanna M. Brandner1,§, Marek Haftek*,2,§ and Carien M. Niessen3,§ 1Department of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, Hamburg, Germany 2University of Lyon, EA4169 Normal and Pathological Functions of Skin Barrier, E. Herriot Hospital, Lyon, France 3Department of Dermatology, Center for Molecular Medicine, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Germany Abstract: The skin is an indispensable barrier which protects the body from the uncontrolled loss of water and solutes as well as from chemical and physical assaults and the invasion of pathogens. In recent years several studies have suggested an important role of intercellular junctions for the barrier function of the epidermis. In this review we summarize our knowledge of the impact of adherens junctions, (corneo)-desmosomes and tight junctions on barrier function of the skin. Keywords: Cadherins, catenins, claudins, cell polarity, stratum corneum, skin diseases. INTRODUCTION ADHERENS JUNCTIONS The stratifying epidermis of the skin physically separates Adherens junctions are intercellular structures that couple the organism from its environment and serves as its first line intercellular adhesion to the cytoskeleton thereby creating a of structural and functional defense against dehydration, transcellular network that coordinate the behavior of a chemical substances, physical insults and micro-organisms. population of cells. Adherens junctions are dynamic entities The living cell layers of the epidermis are crucial in the and also function as signal platforms that regulate formation and maintenance of the barrier on two different cytoskeletal dynamics and cell polarity. -
Keratinization and Its Disorders
Oman Medical Journal (2012) Vol. 27, No. 5: 348-357 DOI 10. 5001/omj.2012.90 Review Article Keratinization and its Disorders Shibani Shetty, Gokul S. Received: 03 May 2012 / Accepted: 08 July 2012 © OMSB, 2012 Abstract Keratins are a diverse group of structural proteins that form the epithelium (buccal mucosa, labial mucosa) and specialized intermediate filament network responsible for maintaining the mucosa (dorsal surface of the tongue).2 An important aspect structural integrity of keratinocytes. In humans, there are around of stratified squamous epithelia is that the cells undergo a 30 keratin families divided into two groups, namely, acidic and terminal differentiation program that results in the formation basic keratins, which are arranged in pairs. They are expressed in of a mechanically resistant and toughened surface composed of a highly specific pattern related to the epithelial type and stage of cornified cells that are filled with keratin filaments and lack nuclei cellular differentiation. A total of 54 functional genes exist which and cytoplasmic organelles. In these squames, the cell membrane codes for these keratin families. The expression of specific keratin is replaced by a proteinaceous cornified envelope that is covalently genes is regulated by the differentiation of epithelial cells within cross linked to the keratin filaments, providing a highly insoluble the stratifying squamous epithelium. Mutations in most of these yet flexible structure that protects the underlying epithelial cells.1 genes are now associated with specific tissue fragility disorders Keratinization, also termed as cornification, is a process which may manifest both in skin and mucosa depending on the of cytodifferentiation which the keratinocytes undergo when expression pattern. -
Documento Completo
I UNIVERSIDAD NACIONAL DE LA PLATA Facultad de Ciencias Veterinarias Trabajo de tesis realizado como requisito para optar al título de Doctor en Ciencias Veterinarias Depilado enzimático conservador del pelo: Injuria química y mecánica de la epidermis para incrementar los procesos difusivos Garro María Laura Director: Profesor Doctor Barbeito Claudio Realizado en la Cátedra de Histología y Embriología. FCV, UNLP. Y en el Centro de Investigación y Tecnología del Cuero CITEC, M. Gonnet. Miembros del Jurado: Doctor Reinoso Hugo Doctor Sofía Alberto Doctor Drago Hugo 2012 II AGRADECIMIENTOS Este trabajo fue realizado sobre una idea original del Ingeniero Carlos Cantera director del Centro de Investigación y Tecnología del Cuero, CITEC. Llegados al punto de escribir lo realizado en este período de investigación quiero guardar un espacio para dar las gracias a todas las personas que han hecho posible este trabajo En primer lugar, gracias al Profesor Doctor Claudio Barbeito por su generosidad intelectual, darme la oportunidad de trabajar en su equipo, dirigir mi investigación, resolver todas mis dudas durante el trabajo en el laboratorio y durante la redacción, así como por la corrección de la misma, que parecía no tener fin. Gracias a la Doctora Renata Bitar quien se hizo un lugar en la etapa del cuidado de su pequeña hija para acompañarme en este trabajo a pesar de la distancia. Al Doctor Néstor Massa por darme la oportunidad de trabajar en Brasil y contactar a Renata. A la Doctora Betina Galarza dispuesta siempre a resolver mis dudas y compartir sus conocimientos. Al Histotecnólogo Rubén Mario por su colaboración en el desarrollo de las técnicas histológicas que fueron una parte indispensable para que esta investigación se pudiera llevar a cabo. -
Sweat Glands
Anatomy & physiology of skin Skin Structure Skin is the single largest organ in the human body. It weighs an average of 4 kg and covers an area of 2 m2 Three distinct layers Epidermis: Composed of epithelial tissue Dermis: Composed of a combination of connective tissues Hypodermis: usually contains abundant fat. Epidermis It’s outermost layer of skin. It consists of many layers of closely packed cells. The most superficial of which areflattened and filled with keratins. It is a stratified squamous epithelium. Contains no blood vessels. It varies in thickness from less than 0.1 mm on the eyelids to nearly 1 mm on the palms and soles. Stratum Basale the deepest layer, rests on a basement membrane, which attaches it to the dermis. It is a single layer of columnar cells. In normal skin only 30% of basal cells are preparing for division. Once basal cell leaves basal layer in humans, normal transit time to stratum corneum is at least 14 days, and transit through stratum corneum to desquamation requires 14 days, 28 days total. Stratum Spinosum Consists of 8-10 layers of Keratinocytes. They are named for the spine-like appearance of the cell margins in histologic sections. As these cells differentiate and move upward through the epidermis, they become progressively flatter and develop organelles known as lamellar granules Composed of Keratinocytes attached to each other via desmosomes. Contains langerhans cells that aid in the immune system response. Stratum Granulosum Stratum Granulosum: The middle layer of 3-5 layers of cells that help form keratin. Contains keratohyline granules that produce a secretion These make up the thick and tough peripheral protein coating of the horny envelope. -
The Appearance of Pili Annulati Following Alopecia Areata
The Appearance of Pili Annulati Following Alopecia Areata Antonio P. Cruz, MD; Christine A. Liang, MD; Jennifer P. Gray, MD; Leslie Robinson-Bostom, MD; Charles J. McDonald, MD Pili annulati is a rare autosomal-dominant hair taking omeprazole. She was otherwise healthy and shaft abnormality. It is characterized by alternat- reported no other nail, hair, or scalp changes. Her ing light and dark bands along the shaft due to family history was positive for eczema, but she denied air-filled cavities within the cortex of the hair shaft. a history of psoriasis or any dermatologic malignancy. Alopecia areata has been previously described Initial examination of the scalp revealed a 632-cm as a common association with pili annulati, with area of alopecia with exclamation point hairs at the improvement in alopecia areata coinciding with periphery. A clinical diagnosis of alopecia areata resolution of pili annulati. We report the case was made. The patient was given a 40-mg intra- of a patient with a history of alopecia areata muscular dose of triamcinolone acetonide and also and alopecia universalis who developed the was prescribed clobetasol propionate gel 0.05% that characteristic banded hair of pili annulati upon she was directed to apply once daily to the affected resolution of her alopecia areata. We provide areas of the scalp. On the 6-week follow-up as well as direct microscopic examinationCUTIS of postregrowth 3 subsequent visits over the course of 8 to 10 months, hairs compared to normal and cross-polarized the patient showed improvement of her alopecia with light microscopy. remarkable regrowth. -
433 Dermatology Team Structure of Skin
433 Dermatology Team structure of skin Lecture (4) Structure of skin [email protected] 1 | P a g e 433 Dermatology Team structure of skin Objectives: • To be familiar with the different structures of the skin. • To have basic knowledge of anatomy and function of the skin. • To be familiar with different tools to investigate skin disorders. • The relation between anatomy and diseases. • To have a general idea about different therapeutic options used in dermatology practice. Color index: slides, doctor notes, 432 notes 2 | P a g e 433 Dermatology Team structure of skin Functions of Skin: Prevent infections via innate and adaptive immunity Maintain a barrier Repair injury Provide circulation Communicate Provide nutrition Regulate temperature Attract attention Pathologies affecting functions of skin: Infections Autoimmunity Cancers Dehydration Eczema Ulcers Infarction Vasculitis Sensory neuropathy Pruritus Vitiligo Alopecia Hyperthermia Vitamin D deficiency The Skin as an organ: General structure and embryological origins Epidermis (ectoderm) Dermal- Epidermal junction is called basement membrane, Weakest part in the skin usual site of blisters Dermis (mesoderm) Subcutaneous fat and skin appendages (ectoderm and mesoderm Palms, soles, genitalia and scalp skin have slightly different structure 3 | P a g e 433 Dermatology Team structure of skin Epidermis: • Keratinocytes: 95% of the cells in epidermis. Division of these cells only occur in the basal layer where 10% of them are stem cells. • The normal transit time of a differentiating keratinocyte from basal layer to the outer surface of the stratum corneum is 28 days. (in psoriasis it is much shorter). • The epidermis doesn’t have blood vessels it obtains its nutrients from the blood vessel of dermis diffusing through the dermoeoidermal junction (papillary layer of dermis). -
MODULE 1 – Week 2 Skin Structure & Function/ Burn
MODULE 1 – Week 2 Skin Structure & Function/ Burn Pathophysiology – The Structure & Function of Normal Skin [1] – The Epidermis Navsaria/ McKenzie The Structure & Function of Skin The integument comprises the skin together with its appendages (Figures 1 & 2). These include hair and hair follicles, sebaceous and sweat glands, and nails. The skin covers the entire body and is the largest organ of the body. It covers a surface area of more than 1.7 m2 making up in total about 16% of normal body weight. It has an array of functions. These include acting as a barrier to physical, biological and chemical agents, as well as to ultraviolet (UV) radiation. Skin barrier function also acts to prevent dehydration by controlling loss and gain of fluid. Other functions include sensory and thermoregulatory roles, vitamin D synthesis, immune surveillance, excretion of wastes through sweat glands, socio- sexual communication and reproduction, by virtue of its appearance and smell (e.g. hormones and pheromones). Skin is divided into glabrous (covering the palms of the hands and soles of the feet) and hairy skin. The skin comprises of 2 layers, the outer most epidermis and the innermost layer, the dermis. Embryologically, these 2 layers of skin are derived from the ectoderm and mesoderm respectively. The epidermis and dermis are firmly attached to each other and together, vary in thickness from around 0.5 to 4 mm or more depending on body site. At the point where the epidermis meets the dermis, evaginations that project into the dermis are formed known as ‘rete ridges’ or ‘pegs’. Complementary projections of the dermis are called dermal papillae. -
Unusually Complex Basement Membranes in the Midgut of Two Decapod Crustaceans, the Stone Crab (Menippe Mercenaria) and the Lobster (Homarus Americanus)
7/ THE ANATOMICAL RECORD 200:253-258 (1981) Unusually Complex Basement Membranes in the Midgut of Two Decapod Crustaceans, the Stone Crab (Menippe mercenaria) and the Lobster (Homarus americanus) JAN ROBERT FACTOR Smithsonian Institution, Ft. Pierce Bureau, Ft. Pierce, Florida 33450 ABSTRACT UltrastructuraJ studies of the stone crab (Menippe mercenaria) and the lobster [Homarus americanus) demonstrate that the basement membrane of the midgut (intestine) is unusually complex. In both species, the basement membrane is three-layered and has processes that form extensive networks pro- truding into the connective tissue. The possible functional significance of this complex structure is discussed. The basement membrane underlying epithe- clude cylinders or grid-like patterns, some- lial tissues is generally considered to be a con- times composed of hexagonal units. tinuous, electron-dense, extracellular sheet Ultrastructural studies of the connective tis- which ranges in thickness from 200 to 50,000 sue layer surrounding the digestive epithelium A and often appears fibrous or flocculent. in two decapod crustaceans, the stone crab When viewed at low magnifications, it has Menippe mercenaria (Brachyura: Xanthidae) been variously described in textbooks as and the lobster Homarus americanus "amorphous" (Threadgold, 76) or "homogene- (Macrura: Nephropidae), demonstrate that the ous" with poorly defined inner and outer limits basement membrane of the adult midgut (Fawcett, '66). Closer examination shows that (intestine) is unusually complex. This is the this layer may be a mat or meshwork of fine fil- first description of a complex basement aments embedded in an amorphous matrix membrane in this major group of (Bloom and Fawcett, 75). The basement mem- invertebrates.