Chapter 20: Nails and Manicuring TOPICS
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Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
International Journal of Molecular Sciences Review Development and Maintenance of Epidermal Stem Cells in Skin Adnexa Jaroslav Mokry * and Rishikaysh Pisal Medical Faculty, Charles University, 500 03 Hradec Kralove, Czech Republic; [email protected] * Correspondence: [email protected] Received: 30 October 2020; Accepted: 18 December 2020; Published: 20 December 2020 Abstract: The skin surface is modified by numerous appendages. These structures arise from epithelial stem cells (SCs) through the induction of epidermal placodes as a result of local signalling interplay with mesenchymal cells based on the Wnt–(Dkk4)–Eda–Shh cascade. Slight modifications of the cascade, with the participation of antagonistic signalling, decide whether multipotent epidermal SCs develop in interfollicular epidermis, scales, hair/feather follicles, nails or skin glands. This review describes the roles of epidermal SCs in the development of skin adnexa and interfollicular epidermis, as well as their maintenance. Each skin structure arises from distinct pools of epidermal SCs that are harboured in specific but different niches that control SC behaviour. Such relationships explain differences in marker and gene expression patterns between particular SC subsets. The activity of well-compartmentalized epidermal SCs is orchestrated with that of other skin cells not only along the hair cycle but also in the course of skin regeneration following injury. This review highlights several membrane markers, cytoplasmic proteins and transcription factors associated with epidermal SCs. Keywords: stem cell; epidermal placode; skin adnexa; signalling; hair pigmentation; markers; keratins 1. Epidermal Stem Cells as Units of Development 1.1. Development of the Epidermis and Placode Formation The embryonic skin at very early stages of development is covered by a surface ectoderm that is a precursor to the epidermis and its multiple derivatives. -
Hair Histology As a Tool for Forensic Identification of Some Domestic Animal Species
EXCLI Journal 2018;17:663-670 – ISSN 1611-2156 Received: June 28, 2018, accepted: July 02, 2018, published: July 06, 2018 Original article: HAIR HISTOLOGY AS A TOOL FOR FORENSIC IDENTIFICATION OF SOME DOMESTIC ANIMAL SPECIES Yasser A. Ahmed1, Safwat Ali2, Ahmed Ghallab3* 1 Department of Histology, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt 2 Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Minia University, Minia, Egypt 3 Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt * Corresponding author: E-mail: [email protected] http://dx.doi.org/10.17179/excli2018-1478 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/). ABSTRACT Animal hair examination at a criminal scene may provide valuable information in forensic investigations. How- ever, local reference databases for animal hair identification are rare. In the present study, we provide differential histological analysis of hair of some domestic animals in Upper Egypt. For this purpose, guard hair of large rumi- nants (buffalo, camel and cow), small ruminants (sheep and goat), equine (horse and donkey) and canine (dog and cat) were collected and comparative analysis was performed by light microscopy. Based on the hair cuticle scale pattern, type and diameter of the medulla, and the pigmentation, characteristic differential features of each animal species were identified. The cuticle scale pattern was imbricate in all tested animals except in donkey, in which coronal scales were identified. The cuticle scale margin type, shape and the distance in between were characteristic for each animal species. -
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. -
Neural Control of Facial Sweat Gland Secretion in Horses
Iowa State University Capstones, Theses and Creative Components Dissertations Fall 2019 Neural control of facial sweat gland secretion in horses Lu Liu Follow this and additional works at: https://lib.dr.iastate.edu/creativecomponents Part of the Comparative and Evolutionary Physiology Commons, and the Systems and Integrative Physiology Commons Recommended Citation Liu, Lu, "Neural control of facial sweat gland secretion in horses" (2019). Creative Components. 455. https://lib.dr.iastate.edu/creativecomponents/455 This Creative Component is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Creative Components by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Neural control of facial sweat gland secretion in horses Lu Liu 2019.11.26 BMS 599 Creative Component Biomedical Sciences Department Iowa State University Abstract: For sweat glands, it has been shown that sympathetic neurons express a cholinergic/noradrenergic co-phenotype in their innervation in the trunk of mice.(Schütz et al. 2008). It is unknown if facial sweat glands are innervated the same way. Gustatory sweating is an abnormal sweating condition. People can sweat profusely when eating or drinking, or even thinking about eating or drinking. We hypothesize that the facial sweat glands are controlled differently and can be related to parasympathetic neurons from cranial nerves. Some samples from human donors have been tested, but few sweat glands can be targeted since the donors were older people. Thus, it was decided to use horse tissue for this project to obtain greater numbers of sweat glands on the face. -
The Integumentary System
CHAPTER 5: THE INTEGUMENTARY SYSTEM Copyright © 2010 Pearson Education, Inc. OVERALL SKIN STRUCTURE 3 LAYERS Copyright © 2010 Pearson Education, Inc. Figure 5.1 Skin structure. Hair shaft Dermal papillae Epidermis Subpapillary vascular plexus Papillary layer Pore Appendages of skin Dermis Reticular • Eccrine sweat layer gland • Arrector pili muscle Hypodermis • Sebaceous (oil) gland (superficial fascia) • Hair follicle Nervous structures • Hair root • Sensory nerve fiber Cutaneous vascular • Pacinian corpuscle plexus • Hair follicle receptor Adipose tissue (root hair plexus) Copyright © 2010 Pearson Education, Inc. EPIDERMIS 4 (or 5) LAYERS Copyright © 2010 Pearson Education, Inc. Figure 5.2 The main structural features of the skin epidermis. Keratinocytes Stratum corneum Stratum granulosum Epidermal Stratum spinosum dendritic cell Tactile (Merkel) Stratum basale Dermis cell Sensory nerve ending (a) Dermis Desmosomes Melanocyte (b) Melanin granule Copyright © 2010 Pearson Education, Inc. DERMIS 2 LAYERS Copyright © 2010 Pearson Education, Inc. Figure 5.3 The two regions of the dermis. Dermis (b) Papillary layer of dermis, SEM (22,700x) (a) Light micrograph of thick skin identifying the extent of the dermis, (50x) (c) Reticular layer of dermis, SEM (38,500x) Copyright © 2010 Pearson Education, Inc. Figure 5.3a The two regions of the dermis. Dermis (a) Light micrograph of thick skin identifying the extent of the dermis, (50x) Copyright © 2010 Pearson Education, Inc. Q1: The type of gland which secretes its products onto a surface is an _______ gland. 1) Endocrine 2) Exocrine 3) Merocrine 4) Holocrine Copyright © 2010 Pearson Education, Inc. Q2: The embryonic tissue which gives rise to muscle and most connective tissue is… 1) Ectoderm 2) Endoderm 3) Mesoderm Copyright © 2010 Pearson Education, Inc. -
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 -
Nails Develop from Thickened Areas of Epidermis at the Tips of Each Digit Called Nail Fields
Nail Biology: The Nail Apparatus Nail plate Proximal nail fold Nail matrix Nail bed Hyponychium Nail Biology: The Nail Apparatus Lies immediately above the periosteum of the distal phalanx The shape of the distal phalanx determines the shape and transverse curvature of the nail The intimate anatomic relationship between nail and bone accounts for the bone alterations in nail disorders and vice versa Nail Apparatus: Embryology Nail field develops during week 9 from the epidermis of the dorsal tip of the digit Proximal border of the nail field extends downward and proximally into the dermis to create the nail matrix primordium By week 15, the nail matrix is fully developed and starts to produce the nail plate Nails develop from thickened areas of epidermis at the tips of each digit called nail fields. Later these nail fields migrate onto the dorsal surface surrounded laterally and proximally by folds of epidermis called nail folds. Nail Func7on Protect the distal phalanx Enhance tactile discrimination Enhance ability to grasp small objects Scratching and grooming Natural weapon Aesthetic enhancement Pedal biomechanics The Nail Plate Fully keratinized structure produced throughout life Results from maturation and keratinization of the nail matrix epithelium Attachments: Lateral: lateral nail folds Proximal: proximal nail fold (covers 1/3 of the plate) Inferior: nail bed Distal: separates from underlying tissue at the hyponychium The Nail Plate Rectangular and curved in 2 axes Transverse and horizontal Smooth, although -
Curling Cuticles of the Great Toenails: a Case Report of Eponychogryphosis
Open Access Case Report DOI: 10.7759/cureus.3959 Curling Cuticles of the Great Toenails: A Case Report of Eponychogryphosis Philip R. Cohen 1 1. Dermatology, San Diego Family Dermatology, San Diego, USA Corresponding author: Philip R. Cohen, [email protected] Abstract The cuticle, also referred to as the eponychium, creates a seal between the proximal nail fold and the nail plate. It is derived from both the ventral and dorsal portions of the proximal nail fold. In addition to its principle function as a barrier preventing allergens, irritants and pathogens from entering the nail cul-de- sac, the cuticle can play a role as a model for evaluating the etiology and management of diseases that affect capillary microcirculation, provide a source of solid tissue for genetic disorder studies, and aid in the evaluation of patients in whom the diagnoses of either systemic scleroderma or dermatomyositis is being entertained. Curling cuticle is a distinctive and unique occurrence. The clinical features of a man with curling cuticles on the lateral portion of both great toes is described. Although a deficiency in personal hygiene may partially account for the clinical finding, the pathogenesis of this observation remains to be established. The term ‘eponychogryphosis’ is proposed to describe the alteration of the patient’s cuticles. Categories: Dermatology, Internal Medicine, Rheumatology Keywords: curl, curling, cuticle, eponychium, eponychogryphosis, fold, great, onychogryphosis, nail, toe Introduction The cuticle, also known as the eponychium, is an extension of the stratum corneum from the proximal nail fold [1-3]. It forms a seal that prevents allergens, irritants, and pathogens from entering the potential space between the distal skin of the digit and the nail plate [4-5]. -
Basic Biology of the Skin 3
© Jones and Bartlett Publishers, LLC. NOT FOR SALE OR DISTRIBUTION CHAPTER Basic Biology of the Skin 3 The skin is often underestimated for its impor- Layers of the skin: tance in health and disease. As a consequence, it’s frequently understudied by chiropractic students 1. Epidermis—the outer most layer of the skin (and perhaps, under-taught by chiropractic that is divided into the following fi ve layers school faculty). It is not our intention to present a from top to bottom. These layers can be mi- comprehensive review of anatomy and physiol- croscopically identifi ed: ogy of the skin, but rather a review of the basic Stratum corneum—also known as the biology of the skin as a prerequisite to the study horny cell layer, consisting mainly of kera- of pathophysiology of skin disease and the study tinocytes (fl at squamous cells) containing of diagnosis and treatment of skin disorders and a protein known as keratin. The thick layer diseases. The following material is presented in prevents water loss and prevents the entry an easy-to-read point format, which, though brief of bacteria. The thickness can vary region- in content, is suffi cient to provide a refresher ally. For example, the stratum corneum of course to mid-level or upper-level chiropractic the hands and feet are thick as they are students and chiropractors. more prone to injury. This layer is continu- Please refer to Figure 3-1, a cross-sectional ously shed but is replaced by new cells from drawing of the skin. This represents a typical the stratum basale (basal cell layer). -
Anatomy and Physiology of the Nail
Anatomy and physiology of the nail Christian Dumontier Institut de la Main & hôpital saint Antoine, Paris Anatomy of the nail • The osteo-ligamentous support • Nail plate • All surrounding tissues, i.e. the perionychium The distal phalanx • Is reinforced laterally by the the Flint’s ligament • Which protect the neuro-vascular structures Flint’s ligament The ligamentous support • The nail is fixed onto the bone through a highly vascularized dermis • The nail is fixed onto the bone through two strong ligaments The ligamentous structures • All the ligaments merge together with • The extensor tendon • The flexor tendon • The collateral ligaments • Flint’s ligament • Guero’s dorsal ligament • (Hyponychial ligament) Clinical implications • A normal nail cannot grow on an abnormal support +++ • Large phalanx = racket nails • bony malunion = nail dystrophy • arthrosis = Pincer nail,... The nail plate • Is produced by the germinal matrix • ItsKeratinic shape depends structure, on the bonypartiall supporty transparent and the and integritycurved both of the longitudinall soft-tissuesy arandound transv it ersally • Three different layers • 0,5 mm thickness, 20% of water Clinical applications • The nail plate is often intact in crushing trauma due to its flexibility • And must be removed in order to explore all the lesions +++ The perionychium • Include all the soft- tissues located under the nail plate • Nail (germinal) matrix, • Nail bed, • Hyponychium The perionychium • Soft-tissues aroud the plate (paronychium) proximal and lateral nail wall (fold) -
The Nail Bed, Part I. the Normal Nail Bed Matrix, Stem Cells, Distal Motion and Anatomy
Central Journal of Dermatology and Clinical Research Review Article *Corresponding author Nardo Zaias, Department of Dermatology Mount Sinai Medical Center, Miami Beach, FL. 33140, 4308 The Nail Bed, Part I. The Normal Alton rd. Suite 750, USA, Email: [email protected] Submitted: 25 November 2013 Nail Bed Matrix, Stem Cells, Distal Accepted: 28 December 2013 Published: 31 December 2013 Copyright Motion and Anatomy © 2014 Zaias Nardo Zaias* OPEN ACCESS Department of Dermatology Mount Sinai Medical Center, USA Abstract The nail bed (NB) has its own matrix that originates from distinctive stem cells. The nail bed matrix stem cells (NBMSC) lie immediately distal to the nail plate (NP) matrix cells and are covered by the keratogenous zone of the most distal NPM (LUNULA). The undivided NBMS cells move distally along the NB basement membrane toward the hyponychium; differentiating and keratinizing at various locations, acting as transit amplifying cells and forming a thin layer of NB corneocytes that contact the overlying onychocytes of the NP, homologous to the inner hair root sheath. At the contact point, the NB corneocytes express CarcinoEmbryonic Antigen (CEA), a glycoprotein-modulating adherence which is also found in hair follicles and tumors. Only when both the NP and the NB are normal do they synchronously move distally. The normal NB keratinizes, expressing keratin K-5 and K-17 without keratohyaline granules. However, during trauma or disease states, it reverts to keratinization with orthokeratosis and expresses K-10, as seen in developmental times. Psoriasis is the only exception. Nail Bed epidermis can express hyperplasia and giant cells in some diseases. -
Keratinocyte-Specific Ablation of the NF-&Kappa
Cell Death and Differentiation (2011) 18, 1845–1853 & 2011 Macmillan Publishers Limited All rights reserved 1350-9047/11 www.nature.com/cdd Keratinocyte-specific ablation of the NF-jB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis S Lippens1,2, S Lefebvre3, B Gilbert1,2, M Sze1,2, M Devos1,2, K Verhelst1,2, L Vereecke1,2, C Mc Guire1,2, C Gue´rin1,2, P Vandenabeele1,2, M Pasparakis4, ML Mikkola3, R Beyaert1,2,5, W Declercq*,1,2,5 and G van Loo1,2,5 The ubiquitin-editing enzyme A20 (tumor necrosis factor-a-induced protein 3) serves as a critical brake on nuclear factor jB (NF-jB) signaling. In humans, polymorphisms in or near the A20 gene are associated with several inflammatory disorders, including psoriasis. We show here that epidermis-specific A20-knockout mice (A20EKO) develop keratinocyte hyperproliferation, but no signs of skin inflammation, such as immune cell infiltration. However, A20EKO mice clearly developed ectodermal organ abnormalities, including disheveled hair, longer nails and sebocyte hyperplasia. This phenotype resembles that of mice overexpressing ectodysplasin-A1 (EDA-A1) or the ectodysplasin receptor (EDAR), suggesting that A20 negatively controls EDAR signaling. We found that A20 inhibited EDAR-induced NF-jB signaling independent from its de-ubiquitinating activity. In addition, A20 expression was induced by EDA-A1 in embryonic skin explants, in which its expression was confined to the hair placodes, known to be the site of EDAR expression. In summary, our data indicate that EDAR-induced NF-jB levels are controlled by A20, which functions as a negative feedback regulator, to assure proper skin homeostasis and epidermal appendage development.