Development of the Urinary System
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3 Embryology and Development
BIOL 6505 − INTRODUCTION TO FETAL MEDICINE 3. EMBRYOLOGY AND DEVELOPMENT Arlet G. Kurkchubasche, M.D. INTRODUCTION Embryology – the field of study that pertains to the developing organism/human Basic embryology –usually taught in the chronologic sequence of events. These events are the basis for understanding the congenital anomalies that we encounter in the fetus, and help explain the relationships to other organ system concerns. Below is a synopsis of some of the critical steps in embryogenesis from the anatomic rather than molecular basis. These concepts will be more intuitive and evident in conjunction with diagrams and animated sequences. This text is a synopsis of material provided in Langman’s Medical Embryology, 9th ed. First week – ovulation to fertilization to implantation Fertilization restores 1) the diploid number of chromosomes, 2) determines the chromosomal sex and 3) initiates cleavage. Cleavage of the fertilized ovum results in mitotic divisions generating blastomeres that form a 16-cell morula. The dense morula develops a central cavity and now forms the blastocyst, which restructures into 2 components. The inner cell mass forms the embryoblast and outer cell mass the trophoblast. Consequences for fetal management: Variances in cleavage, i.e. splitting of the zygote at various stages/locations - leads to monozygotic twinning with various relationships of the fetal membranes. Cleavage at later weeks will lead to conjoined twinning. Second week: the week of twos – marked by bilaminar germ disc formation. Commences with blastocyst partially embedded in endometrial stroma Trophoblast forms – 1) cytotrophoblast – mitotic cells that coalesce to form 2) syncytiotrophoblast – erodes into maternal tissues, forms lacunae which are critical to development of the uteroplacental circulation. -
Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Structure of Pronephros and Development of Mesonephric Kidney in Larvae of Russian Sturgeon, Acipenser Gueldenstaedtii Brandt (Acipenseridae)
Zoologica5 PRONEPHROS Poloniae-AND (2012)-MESONEPHRIC 57/1-4: 5-20-KIDNEY-IN-LARVAE-OF-A.-GUELDENSTAEDTII 5 DOI: 10.2478/v10049-012-0001-6 STRUCTURE OF PRONEPHROS AND DEVELOPMENT OF MESONEPHRIC KIDNEY IN LARVAE OF RUSSIAN STURGEON, ACIPENSER GUELDENSTAEDTII BRANDT (ACIPENSERIDAE) L.S. KRAYUSHKINA*1, A.A. GERASIMOV1, A.A. KIRSANOV1, M.V. MOSYAGINA1, A. OGORZA£EK2 1Department of Ichthyology and Hydrobiology, St. Petersburg State University, 16-th Line 29, 199178, St. Petersburg, Russia, [email protected] 2 Department of Animal Developmental Biology, Zoological Institute, University of Wroclaw, Sienkiewicza 21, 50-335 Wroclaw, Poland. *Corresponding author Abstract. The structure of the pronephros and development of mesonephric kidney in Russian sturgeon larvae, Acipenser gueldenstaedtii Brandt at different stages of early postembryonic development (from hatching to 14 days), were studied with histological and electronic microscopy methods. The larval pronephros is represented by the system of bilaterally located pronephric tubules with ciliated nephrostomes and funnels and exog- enous single glomus, which is not integrated directly into pronephric tubules and located in the pronephric chamber. The glomus is positioned below the dorsal aorta and vascular- ized by its capillaries. The glomus has the same features of the thin structure that are typical of and necessary for the function of a filtering organ. The structure of the prone- phros in acipenserids is discussed and compared with teleosts and amphibians. Histogen- esis of the mesonephric kidney is observed during the period of pronephros functioning; it is complete by the time the larvae transfer to exogenous feeding. At this moment, the pronephros undergoes significant structural degradation. -
Essential Roles of Inhibin Beta a in Mouse Epididymal Coiling
Essential roles of inhibin beta A in mouse epididymal coiling Jessica Tomaszewski*, Avenel Joseph†, Denise Archambeault†, and Humphrey Hung-Chang Yao†‡ *Department of Biology, School of Integrative Biology, and †Department of Veterinary Biosciences, College of Veterinary Medicine, University of Illinois at Urbana–Champaign, Urbana, IL 61802 Edited by Jean D. Wilson, University of Texas Southwestern Medical Center, Dallas, TX, and approved May 29, 2007 (received for review April 13, 2007) Testis-derived testosterone has been recognized as the key factor appear to be indirect via a mesenchyme-derived regulator(s). When for morphogenesis of the Wolffian duct, the precursor of several the upper Wolffian duct epithelium (the future epididymis) was male reproductive tract structures. Evidence supports that testos- grafted onto the lower Wolffian duct mesenchyme (the future terone is required for the maintenance of the Wolffian duct via its seminal vesicle), the epithelium underwent seminal vesicle mor- action on the mesenchyme. However, it remains uncertain how phogenesis and expressed markers specific for seminal vesicle testosterone alone is able to facilitate formation of regionally epithelium instead of those for epididymal epithelium (10). This specific structures such as the epididymis, vas deferens, and sem- inductive ability of Wolffian duct mesenchyme was also found in the inal vesicle from a straight Wolffian duct. In this study, we iden- prostate, providing further support that AR in the mesenchyme is tified inhibin beta A (or Inhba) as a regional paracrine factor in necessary to dictate androgenic actions of the epithelium (11). mouse mesonephroi that controls coiling of the epithelium in the Furthermore, when the epithelium from the AR-deficient testicular anterior Wolffian duct, the future epididymis. -
Development of the Female Reproductive System
Development of the female Reproductive System Dr. Susheela Rani Genital System •Gonads •Internal genitals •External genitals Determining sex – chronology of events •Determined Genetic sex at fertilization Gonadal sex •6th week Phenotypic sex •Differentiation of Behavioural Psyche - Preoptic and Median region Sex of Hypothalamus Genetic Sex Genetic sex of an embryo is determined at the time of fertilization, depending on whether the spermatocyte carries an X or a Y chromosome. The ‘Master’ Gene that determines Gender • SRY (Sex determining Region Y gene) • Has a testis-determining effect on the indifferent gonads. • Small gene (a single exon) • Localized on the shorter arm of the Y chromosome (Yp) • Gets expressed in the gonadal cells • Controls a whole number of further genes on the autosomes as well as on the X chromosome. • Causes development of Testes • Pseudo autosomal regions PAR1 and PAR 2 – Yellow • Heterochromatin – redundant DNA sequences – Pink • SRY – Region for Sex Determining Gene- Dark red • ZFY , Y linked Zinc Finger Protein – Orange • Spermatogenesis Genes in long arm – Azoospermia factor AZF • Telomeres – green • Centromeres - Blue It is not the number of gonosomes that is decisive for the gender, but rather the presence or absence of the Y-chromosome Aneuploidy and Euploidy of Gonosomes Karyotype Phenotypic Gonad Syndrome Fate Gender 45, XO Female Ovaries Turner’s Atrophy of Ovaries in the fetus 45, YO ------ ----- ----- Absence of X chromosome is lethal 46, XX Female Ovaries Normal Normal Development Woman 47, XXX Female -
Scrotal Ultrasound
Scrotal Ultrasound Bruce R. Gilbert, MD, PhD Associate Clinical Professor of Urology & Reproductive Medicine Weill Cornell Medical College Director, Reproductive and Sexual Medicine Smith Institute For Urology North Shore LIJ Health System 1 Developmental Anatomy" Testis and Kidney Hindgut Allantois In the 3-week-old embryo the Primordial primordial germ cells in the wall of germ cells the yolk sac close to the attachment of the allantois migrate along the Heart wall of the hindgut and the dorsal Genital Ridge mesentery into the genital ridge. Yolk Sac Hindgut At 5-weeks the two excretory organs the pronephros and mesonephros systems regress Primordial Pronephric system leaving only the mesonephric duct. germ cells (regressing) Mesonephric The metanephros (adult kidney) system forms from the metanephric (regressing) diverticulum (ureteric bud) and metanephric mass of mesoderm. The ureteric bud develops as a dorsal bud of the mesonephric duct Cloaca near its insertion into the cloaca. Mesonephric Duct Mesonephric Duct Ureteric Bud Ureteric Bud Metanephric system Metanephric system 2 Developmental Anatomy" Wolffian and Mullerian DuctMesonephric Duct Under the influence of SRY, cells in the primitive sex cords differentiate into Sertoli cells forming the testis cords during week 7. Gonads Mesonephros It is at puberty that these testis cords (in Paramesonephric association with germ cells) undergo (Mullerian) Duct canalization into seminiferous tubules. Mesonephric (Wolffian) Duct At 7 weeks the indifferent embryo also has two parallel pairs of genital ducts: the Mesonephric (Wolffian) and the Paramesonephric (Mullerian) ducts. Bladder Bladder Mullerian By week 8 the developing fetal testis tubercle produces at least two hormones: Metanephros 1. A glycoprotein (MIS) produced by the Ureter Uterovaginal fetal Sertoli cells (in response to SRY) primordium Rectum which suppresses unilateral development of the Paramesonephric (Mullerian) duct 2. -
Stem Cells in the Embryonic Kidney R Nishinakamura1
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector http://www.kidney-international.org mini review & 2008 International Society of Nephrology Stem cells in the embryonic kidney R Nishinakamura1 1Division of Integrative Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, 2-2-1 Honjo, Kumamoto, Japan The mammalian kidney, the metanephros, is formed by a STRATEGY TOWARD KIDNEY RECONSTITUTION USING reciprocally inductive interaction between two precursor PROGENITOR CELLS tissues, the metanephric mesenchyme and the ureteric bud. Stem cells are defined by two criteria: self-renewal and The ureteric bud induces the metanephric mesenchyme to multipotency. Few reports in the kidney field have addressed differentiate into the epithelia of glomeruli and renal tubules. both of these criteria at a clonal level, so it is better to use the Multipotent renal progenitors that form colonies upon Wnt4 term ‘progenitor’ rather than ‘stem cells.’ In this review, renal stimulation and strongly express Sall1 exist in the progenitors in the embryonic kidney, not those in the adult metanephric mesenchyme; these cells can partially kidney, from the viewpoint of developmental biology and reconstitute a three-dimensional structure in an organ stem/progenitor cell biology will be discussed. To generate culture setting. Six2 maintains this mesenchymal progenitor multiple cell lineages for kidney regeneration, the identifica- population by opposing Wnt4-mediated epithelialization. tion of renal progenitors is a prerequisite. Furthermore, there Upon epithelial tube formation, Notch2 is required for the exist three obstacles to be overcome: (1) derivation of the differentiation of proximal nephron structures (podocyte and renal progenitors; (2) expansion of the renal progenitors; and proximal tubules). -
The Reproductive System
27 The Reproductive System PowerPoint® Lecture Presentations prepared by Steven Bassett Southeast Community College Lincoln, Nebraska © 2012 Pearson Education, Inc. Introduction • The reproductive system is designed to perpetuate the species • The male produces gametes called sperm cells • The female produces gametes called ova • The joining of a sperm cell and an ovum is fertilization • Fertilization results in the formation of a zygote © 2012 Pearson Education, Inc. Anatomy of the Male Reproductive System • Overview of the Male Reproductive System • Testis • Epididymis • Ductus deferens • Ejaculatory duct • Spongy urethra (penile urethra) • Seminal gland • Prostate gland • Bulbo-urethral gland © 2012 Pearson Education, Inc. Figure 27.1 The Male Reproductive System, Part I Pubic symphysis Ureter Urinary bladder Prostatic urethra Seminal gland Membranous urethra Rectum Corpus cavernosum Prostate gland Corpus spongiosum Spongy urethra Ejaculatory duct Ductus deferens Penis Bulbo-urethral gland Epididymis Anus Testis External urethral orifice Scrotum Sigmoid colon (cut) Rectum Internal urethral orifice Rectus abdominis Prostatic urethra Urinary bladder Prostate gland Pubic symphysis Bristle within ejaculatory duct Membranous urethra Penis Spongy urethra Spongy urethra within corpus spongiosum Bulbospongiosus muscle Corpus cavernosum Ductus deferens Epididymis Scrotum Testis © 2012 Pearson Education, Inc. Anatomy of the Male Reproductive System • The Testes • Testes hang inside a pouch called the scrotum, which is on the outside of the body -
Scrotal Ultrasound CONTENT ANATOMY
12/04/2021 Scrotal Ultrasound Scrotal Ultrasound Paul S. Sidhu CONTENT Professor of Imaging Sciences King’s College Hospital London Scrotal Ultrasound Lecture Content • Background Anatomy • Normal Variants • Extra-testicular pathology • Intra-testicular pathology • Global Abnormalities Scrotal Ultrasound • New US techniques ANATOMY Scrotal Ultrasound Scrotal Ultrasound Anatomy Vascular Anatomy • Testicular artery Low vascular resistance Broad systolic peak High diastolic flow • Cremasteric artery and artery to ductus deferens Epididymis/Peri-testicular tissues Narrower systolic peak Low diastolic flow Aziz ZA, Satchithananda K, Khan M, Sidhu PS. High Frequency Colour Doppler Ultrasound of the Spermatic Cord Arteries: Resistive Index Variation in a Cohort of 51 Healthy Men. Journal of Ultrasound in Medicine 2005;24:905-909. 1 12/04/2021 Scrotal Ultrasound Vascular Anatomy • Pampiniform plexus • Cremasteric plexus • Testicular vein Scrotal Ultrasound NORMAL VARIANTS Scrotal Ultrasound Scrotal Ultrasound Normal Variants Normal Variants Torsion of an Appendix Testis • Testicular appendages are remnants of the paramesonephric ducts, found at the upper pole of the testes in a groove between the testis and the head of the • Age range 7-12 years epididymis. • ‘Blue dot’ sign on a fair skin. • Similar reflectivity to the epididymal head and ovoid shaped, may be cystic. • Torsion of a testicular appendix is a common cause for scrotal pain in children. • Appendix is usually sessile but may be pedunculated and sometimes calcifies. • The presenting features of appendicular torsion and testicular torsion are often similar, • Seen in 92% of post mortems, 90% of cases are appendix testis • Infarcted appendix may form a scrotal pearl though pain localised to the upper pole of the testicle and a tender nodule are suggestive of a torsed appendix. -
Secreted Molecules in Metanephric Induction
J Am Soc Nephrol 11: S116–S119, 2000 Secreted Molecules in Metanephric Induction THOMAS J. CARROLL and ANDREW P. McMAHON Department of Molecular and Cellular Biology, Biological Laboratories, Harvard University, Cambridge, Massachusetts. Abstract. Nearly 50 yr ago, Clifford Grobstein made the ob- the classic model of metanephric induction. The studies of the servation that the ureteric bud induced the nephrogenic mes- classic ureteric inducer performed to date have most likely enchyme to undergo tubulogenesis. Since that discovery, sci- been characterizations of a mesenchyme-specific inducer, entists have attempted to characterize the molecular nature of Wnt-4, and its role in tubulogenesis. Ureteric induction most the inducer. To date, no single molecule that is both necessary likely involves a series of distinct events that provide prolif- and sufficient for nephric induction has been identified. Be- erative, survival, and condensation signals to the mesenchyme, cause of recent insights regarding the role of several secreted integrating the growth of the ureteric system with tubulogen- molecules in tubulogenesis, it has become necessary to revise esis. The developmental biologic processes of the kidney have been logenesis. The conclusion drawn from this discovery was that the subject of intense study for more than 100 yr (for review, the ureteric bud induces tubulogenesis within the surrounding see reference (1). All three vertebrate kidney types (pro- mesenchyme. During further investigation, it was discovered nephros, mesonephros, and metanephros) are derivatives of a that a number of tissues, including, most notably, a dorsal region of the embryo known as the intermediate mesoderm. In portion of the embryonic spinal cord, are able to substitute for mice, a portion of the mesonephric duct, known as the meta- the ureter in this inductive interaction. -
Clinical Pelvic Anatomy
SECTION ONE • Fundamentals 1 Clinical pelvic anatomy Introduction 1 Anatomical points for obstetric analgesia 3 Obstetric anatomy 1 Gynaecological anatomy 5 The pelvic organs during pregnancy 1 Anatomy of the lower urinary tract 13 the necks of the femora tends to compress the pelvis Introduction from the sides, reducing the transverse diameters of this part of the pelvis (Fig. 1.1). At an intermediate level, opposite A thorough understanding of pelvic anatomy is essential for the third segment of the sacrum, the canal retains a circular clinical practice. Not only does it facilitate an understanding cross-section. With this picture in mind, the ‘average’ of the process of labour, it also allows an appreciation of diameters of the pelvis at brim, cavity, and outlet levels can the mechanisms of sexual function and reproduction, and be readily understood (Table 1.1). establishes a background to the understanding of gynae- The distortions from a circular cross-section, however, cological pathology. Congenital abnormalities are discussed are very modest. If, in circumstances of malnutrition or in Chapter 3. metabolic bone disease, the consolidation of bone is impaired, more gross distortion of the pelvic shape is liable to occur, and labour is likely to involve mechanical difficulty. Obstetric anatomy This is termed cephalopelvic disproportion. The changing cross-sectional shape of the true pelvis at different levels The bony pelvis – transverse oval at the brim and anteroposterior oval at the outlet – usually determines a fundamental feature of The girdle of bones formed by the sacrum and the two labour, i.e. that the ovoid fetal head enters the brim with its innominate bones has several important functions (Fig. -
Glomus Specification and Induction in Xenopus
Development 126, 5847-5856 (1999) 5847 Printed in Great Britain © The Company of Biologists Limited 1999 DEV6378 The specification and growth factor inducibility of the pronephric glomus in Xenopus laevis Hannah C. Brennan, Sarbjit Nijjar and Elizabeth A. Jones* Cell and Molecular Development Group, Department of Biological Sciences, Warwick University, Coventry, CV4 7AL, UK *Author for correspondence (e-mail: [email protected]) Accepted 23 September; published on WWW 24 November 1999 SUMMARY We report a study on the specification of the glomus, the Furthermore, we have analysed the growth factor filtration device of the amphibian pronephric kidney, using inducibility of the glomus in the presence or absence of an explant culturing strategy in Xenopus laevis. Explants of retinoic acid (RA) by RT-PCR. We define for the first time presumptive pronephric mesoderm were dissected from the conditions under which these growth factors induce embryos of mid-gastrula to swimming tadpole stages. These glomus tissue in animal cap tissue. Activin together with explants were cultured within ectodermal wraps and high concentrations of RA can induce glomus tissue from analysed by RT-PCR for the presence of the Wilm’s Tumour- animal cap ectoderm. Unlike the pronephric tubules, the 1 gene, xWT1, a marker specific for the glomus at the stages glomus can also be induced by FGF and RA. analysed, together with other mesodermal markers. We show that the glomus is specified at stage 12.5, the same stage at which pronephric tubules are specified. We have previously shown that pronephric duct is specified somewhat later, at stage 14.