The Female Reproductive System the Female Reproductive System
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In Hardening of the Zona Pellucida K
Disulfide formation in bovine zona pellucida glycoproteins during fertilization: evidence for the involvement of cystine cross-linkages in hardening of the zona pellucida K. Kwamoto, K. Ikeda, N. Yonezawa, S. Noguchi, K. Kudo, S. Hamano, M. Kuwayama and M. Nakano department ofChemistry, Faculty ofScience and 2Graduate School ofScience and Technology, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan; and3Animal Bio-Technology Center, Livestock Improvement Association, Tokyo, Japan The time for solubilization of the bovine zona pellucida in a hypotonic buffer containing 5% (v/v) \g=b\-mercaptoethanoland 7 mol urea l\m=-\1 increased by 10% after fertilization. Coupling with a specific fluorescent thiol probe, monobromobimane (mBBr), was markedly greater in the zona pellucida of ovarian eggs compared with fertilized eggs, indicating that the cysteine residues in the zona pellucida of unfertilized eggs are oxidized to cystines during fertilization. After endo-\g=b\-galactosidasedigestion to remove N-acetyllactosamine repeats of the carbohydrate chains, three zona pellucida glycoproteins (ZPA, ZPB and ZPC) coupled with the fluorescent bimane groups were fractionated efficiently by reverse-phase HPLC. Estimation of bimane groups in the three components and SDS-PAGE revealed that intramolecular disulfide bonds in ZPA and intra- and intermolecular disulfide bonds in ZPB were formed during fertilization, but oxidation of cysteine residues in ZPC was low. Specific proteolysis of ZPA during fertilization was also observed. These results indicate that the formation of disulfide linkages together with specific proteolysis result in the construction of a rigid zona pellucida structure, which is responsible for hardening of the zona pellucida. Introduction cross-linkages between tyrosine residues of the zona pellucida proteins formed by ovoperoxidase caused the The zona is one of the two sites at which pellucida In contrast to sea urchins (Foerder and is blocked and hardening. -
Chapter 28 *Lecture Powepoint
Chapter 28 *Lecture PowePoint The Female Reproductive System *See separate FlexArt PowerPoint slides for all figures and tables preinserted into PowerPoint without notes. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Introduction • The female reproductive system is more complex than the male system because it serves more purposes – Produces and delivers gametes – Provides nutrition and safe harbor for fetal development – Gives birth – Nourishes infant • Female system is more cyclic, and the hormones are secreted in a more complex sequence than the relatively steady secretion in the male 28-2 Sexual Differentiation • The two sexes indistinguishable for first 8 to 10 weeks of development • Female reproductive tract develops from the paramesonephric ducts – Not because of the positive action of any hormone – Because of the absence of testosterone and müllerian-inhibiting factor (MIF) 28-3 Reproductive Anatomy • Expected Learning Outcomes – Describe the structure of the ovary – Trace the female reproductive tract and describe the gross anatomy and histology of each organ – Identify the ligaments that support the female reproductive organs – Describe the blood supply to the female reproductive tract – Identify the external genitalia of the female – Describe the structure of the nonlactating breast 28-4 Sexual Differentiation • Without testosterone: – Causes mesonephric ducts to degenerate – Genital tubercle becomes the glans clitoris – Urogenital folds become the labia minora – Labioscrotal folds -
Formation of the Hamster Zona Pellucida in Relation to Ovarian Differentiation and Follicular Growth M
Formation of the hamster zona pellucida in relation to ovarian differentiation and follicular growth M. C. L\l=e'\veill\l=e'\,K. D. Roberts, S. Chevalier, A. Chapdelaine and G. Bleau Departments of Obstetrics and Gynecology, Biochemistry and Medicine, University of Montreal and Maisonneuve-Rosemont Research Center, Montreal, Quebec, Canada H1T 2M4 Summary. Using an immunofluorescence technique on ovarian sections, zona\x=req-\ immunoreactive components were detected in the cytoplasm of the oocyte from the beginning of its growth, when it is surrounded by only a thin squamous follicular cell layer, up to the end of its growth. In parallel with oocyte growth, the staining intensity decreased in the ooplasm. No staining was observed in the cytoplasm of the granulosa cells during normal follicular development in adult cyclic females. However, staining of the granulosa cells was observed at some stages of follicular development in immature females. This staining was especially evident in the ovaries of immature females (22 or 26 days old) stimulated with PMSG. In addition, the staining of the granulosa cells was consistently observed in ovaries showing an abnormal histology. Increased staining of the zona at its outer and inner regions could be distinguished in normal follicles, but when staining occurred on the granulosa cells no such pattern was observed over the zona matrix. These studies indicate that the oocyte itself but not the granulosa cells elaborates the native immunogenic material of the zona pellucida. The administration of PMSG at particular stages of ovarian differentiation interferes with follicular development leading to an abnormal extracellular assembly of the zona and its degradation (phagocytosis) by the surrounding granulosa cells. -
Changes in the Composition of the Hamster Zona Pellucida After Fertilization in Vivo but Not in Vitro C
Changes in the composition of the hamster zona pellucida after fertilization in vivo but not in vitro C. R. Brown, N. Clarke, M. Aiken and B. D. Bavister Institute of Animal Physiology and Genetics Research, Babraham Hall, Cambridge CB2 4AT, UK; and * Department ofVeterinary Science, University of Wisconsin, Madison, WI53706, USA Summary. Hamster zonae pellucidae were obtained from follicular oocytes, super- ovulated eggs, and eggs fertilized in vivo or in vitro. Zonae were labelled with N-succinimidyl-3(4-hydroxy,5-[125I]iodophenyl)propionate, and compared on single\x=req-\ and two-dimensional SDS-PAGE. Single-dimensional electrophoresis showed consider- able differences between zona categories in the amount of label that they incorporated; follicular zonae incorporated the least label and zonae from eggs fertilized in vivo the most. On two-dimensional electrophoresis, polypeptides from 3 of the 4 zona categories migrated into 4 major groups: two of these groups each with Mr 150 000\p=n-\250000 were within the Mr range of ZP1, and two others, at Mr90 000 and 55 000, appeared to be analogous to ZP2 and ZP3, respectively. The fourth zona category (zonae from eggs fertilized in vivo) showed a changed polypeptide profile as well as incorporating the most label; one of the polypeptides, Mr 150 000\p=n-\250000, was undetectable, but a train of Mr 70 000\p=n-\90000 polypeptides and a discrete polypeptide at Mr 20 000 were new. Since this changed profile did not occur in zonae from superovulated eggs, or in zonae from eggs fertilized in vitro, a synergism between oviducal factors and factors from the spermatozoon or egg, or both, towards the zona in vivo is indicated. -
Embryology J
Embryology J. Matthew Velkey, Ph.D. [email protected] 452A Davison, Duke South Textbook: Langmans’s Medical Embryology, 11th ed. When possible, lectures will be recorded and there may be notes for some lectures, but still NOT a substitute for reading the text. Completing assigned reading prior to class is essential for sessions where a READINESS ASSESSMENT is scheduled. Overall goal: understand the fundamental processes by which the adult form is produced and the clinical consequences that arise from abnormal development. Follicle Maturation and Ovulation Oocytes ~2 million at birth ~40,000 at puberty ~400 ovulated over lifetime Leutinizing Hormone surge (from pituitary gland) causes changes in tissues and within follicle: • Swelling within follicle due to increased hyaluronan • Matrix metalloproteinases degrade surrounding tissue causing rupture of follicle Egg and surrounding cells (corona radiata) ejected into peritoneum Corona radiata provides bulk to facilitate capture of egg. The egg (and corona radiata) at ovulation Corona radiata Zona pellucida (ZP-1, -2, and -3) Cortical granules Transport through the oviduct At around the midpoint of the menstrual cycle (~day 14), a single egg is ovulated and swept into the oviduct. Fertilization usually occurs in the ampulla of the oviduct within 24 hrs. of ovulation. Series of cleavage and differentiation events results in the formation of a blastocyst by the 4th embryonic day. Inner cell mass generates embryonic tissues Outer trophectoderm generates placental tissues Implantation into -
The Uterine Tubal Fluid: Secretion, Composition and Biological Effects
Anim. Reprod., v.2, n.2, p.91-105, April/June, 2005 The uterine tubal fluid: secretion, composition and biological effects J. Aguilar1,2 and M. Reyley1 1Producción Equina, Departamento de Producción Animal, Facultad de Agronomia y Veterinaria, Universidad Nacional de Rio Cuarto, 5800 Rio Cuarto, Córdoba, Argentina 2Division of Veterinary Clinical Studies, University of Edinburgh, Easter Bush Veterinary Centre, Easter Bush EH25 9RG, Scotland, UK Abstract regions of the tube indicate the existence of systemic and local controlling mechanisms of tubal fluid production. Gamete transport, sperm capacitation, fertilization, and early embryo development are all Keywords: uterine tube, oviduct, fluid, composition, physiological events that occur in a very synchronized secretion, fertilization manner within the uterine tubal lumen. The tubal fluid that bathes the male and female gametes allows these Introduction events to occur in vivo much more successfully than in vitro. Collection of tubal fluid from domestic females The uterine tube provides the appropriate has been performed by different methods. The amount environment for oocytes, spermatozoa transport, of fluid secreted by the uterine tube increases during fertilization, and early embryo development. When estrus and decreases during diestrus and pregnancy. The attempts to reproduce any of these events outside the ampulla produces approximately two thirds of the total tubal lumen are made, dramatic drops in efficiency are daily secretion, while the isthmus supplies the rest. consistently seen. This limitation is particularly strong Steroid hormones qualitatively and quantitatively in the mare, where a repeatable in vitro fertilization modify the tubal fluid, through both a direct effect on method has not yet been developed. -
Ans 214 SI Multiple Choice Set 4 Weeks 10/14 - 10/23
AnS 214 SI Multiple Choice Set 4 Weeks 10/14 - 10/23 The following multiple choice questions pertain to material covered in the last two weeks' lecture sets. Answering the following questions will aid your exam preparation. These questions are meant as a gauge of your content knowledge - use them to pinpoint areas where you need more preparation. 1. A heifer begins ovarian activity at A. 6-8 months B. 8-10 months C.10-12 months D. 12-14 months E. 24 months 2. The gestation length of a cow is A. 82 days C. 166 days D. 283 days E. 311 days 3. All of the following produce hormones vital to ovarian cyclicity EXCEPT A. hypothalamus B. ovary C. posterior pituitary D. uterus E. all of the above are correct 4. Which of the following structures is INCORRECTLY matched to the hormones it produces? A. uterus: PGF2a B. ovary: testosterone, activin, estrogen, oxytocin C. placenta: progesterone, testosterone, estrogen D. anterior pituitary: ACTH, FSH, LH E. hypothalamus: GnRH, CRH 5. In the female reproductive system of all species A. the ovaries are supported by the mesometrium B. urine can only exit via the urethra via the suburethral diverticulum C. the uterus produces progesterone D. the oviduct is supported by the mesosalpinx E. the ovary is directly connected to the oviduct 6. Which of the following is FALSE about the mare? A. Ovulates from the medulla because of an inverted ovarian structure B. Ovulates a 2n oocyte C. Does not have a suburethral diverticulum D. Ovulates at only one site on the ovary, called the ovulation fossa E. -
And Theca Interna Cells from Developing Preovulatory Follicles of Pigs B
Differential production of steroids by dispersed granulosa and theca interna cells from developing preovulatory follicles of pigs B. K. Tsang, L. Ainsworth, B. R. Downey and G. J. Marcus * Reproductive Biology Unit, Department of Obstetrics and Gynecology and Department of Physiology, University of Ottawa, Ottawa Civic Hospital, Ottawa, Ontario, Canada Kl Y 4E9 ; tAnimal Research Centre, Agriculture Canada, Ottawa, Ontario, Canada K1A 0C6; and \Department of Animal Science, Macdonald College of McGill University, Ste Anne de Bellevue, Quebec, Canada H9X ICO Summary. Dispersed granulosa and theca interna cells were recovered from follicles of prepubertal gilts at 36, 72 and 108 h after treatment with 750 i.u. PMSG, followed 72 h later with 500 i.u. hCG to stimulate follicular growth and ovulation. In the absence of aromatizable substrate, theca interna cells produced substantially more oestrogen than did granulosa cells. Oestrogen production was increased markedly in the presence of androstenedione and testosterone in granulosa cells but only to a limited extent in theca interna cells. The ability of both cellular compartments to produce oestrogen increased up to 72 h with androstenedione being the preferred substrate. Oestrogen production by the two cell types incubated together was greater than the sum produced when incubated alone. Theca interna cells were the principal source of androgen, predominantly androstenedione. Thecal androgen production increased with follicular development and was enhanced by addition of pregnenolone or by LH 36 and 72 h after PMSG treatment. The ability of granulosa and thecal cells to produce progesterone increased with follicular development and addition of pregnenolone. After exposure of developing follicles to hCG in vivo, both cell types lost their ability to produce oestrogen. -
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. -
Oogenesis/Folliculogenesis Ovarian Follicle Endocrinology
Oogenesis/Folliculogenesis & Ovarian Follicle Endocrinology follicle - composite structure Ovarian Follicle that will produce mature oocyte – primordial follicle - germ cell (oocyte) with a single layer ZP of mesodermal cells around it TI & TE it – as development of follicle progresses, oocyte will obtain a ‘‘halo’’ of cells and membranes that are distinct: Oocyte 1. zona pellucide (ZP) 2. granulosa (Gr) 3. theca interna and externa (TI & TE) Gr Summary: The follicle is the functional unit of the ovary. One female gamete, the oocyte is contained in each follicle. The granulosa cells produce hormones (estrogen and inhibin) that provide ‘status’ signals to the pituitary and brain about follicle development. Mammal - Embryonic Ovary Germ Cells Division and Follicle Formation from Makabe and van Blerkom, 2006 Oogenesis and Folliculogenesis GGrraaaafifiaann FFoolliclliclele SStrtruucctuturree SF-1 Two Cell Steroidogenesis • Common in mammalian ovarian follicle • Part of the steroid pathway in – Granulosa – Theca interna • Regulated by – Hypothalamo-pituitary axis – Paracrine factors blood ATP FSH LH ATP Estradiol-17β FSH-R LH-R mitochondrion cAMP cAMP CHOL P450arom PKA 17βHSD C P450scc PKA C C C cholesterol pool PREG Testosterone StAR 3βHSD Estrone SF-1 PROG 17βHSD P450arom Androstenedione nucleus Andro theca Mammals granulosa Activins & Inhibins Pituitary - Gonadal Regulation of the FSH Adult Ovary E2 Inhibin Activin Follistatin Inhibins and Activins •Transforming Growth Factor -β (TGF-β) family •Many gonadal cells produce β subunits •In -
Invasion of Foreign White Blood Cells Into Vaginal Epithelium Brent Ibata Southern Illinois University Carbondale
Southern Illinois University Carbondale OpenSIUC Honors Theses University Honors Program 12-1995 Invasion of Foreign White Blood Cells into Vaginal Epithelium Brent Ibata Southern Illinois University Carbondale Follow this and additional works at: http://opensiuc.lib.siu.edu/uhp_theses Recommended Citation Ibata, Brent, "Invasion of Foreign White Blood Cells into Vaginal Epithelium" (1995). Honors Theses. Paper 54. This Dissertation/Thesis is brought to you for free and open access by the University Honors Program at OpenSIUC. It has been accepted for inclusion in Honors Theses by an authorized administrator of OpenSIUC. For more information, please contact [email protected]. Invasion of Foreign White Blood Cells into Vaginal Epithelium Brent Ibata Introduction Lymphocytes and macrophages, the tiny warriors of the immune system, constantly patrol the mucosal borders of the body to fend off possible intruders. But can the Common Mucosal Immune System (CMIS) fall prey to a Trojan Horse? HIV infected cells have been theorized to be the Trojan Horse that caries the virus' genetic code to the mucosal barriers of a potential victim. The question is where, in the reproductive tract does the infection initially take root and by which vector? One suggestion is that lymphocytes may transmit HIV to CD4-negative epithelial cells.(Phillips, 1994) Another suggestion is that HIV initially infects host macrophages in the cervical transformational zone.(Nuovo, 1994) It hypothesized here, in this paper, that foreign leukocytes can invade the female reproductive mucosal epithelium and enter into the lymphatic system. This hypothesis is partially supported by the unpublished observations (Quayle, et al 1995) of mononuclear cell adherence and penetration into endocervical epithelium, in-vitro. -
Time and Process of Sperm Penetration Into Hamster Ova in Vivo and in Vitro
TIME AND PROCESS OF SPERM PENETRATION INTO HAMSTER OVA IN VIVO AND IN VITRO R. YANAGIMACHI Worcester Foundation for Experimental Biology, Shrewsbury, Massachusetts, U.S.A., and Z°°l°Sical Institute, Faculty of Science, Hokkaido University, Sapporo, Japan {Received 18th September 1965) Summary. Female golden hamsters were mated at various times before or after ovulation, and the time of sperm penetration into the ova was examined. When the females were mated several hours prior to ovula- tion, penetration of spermatozoa into the ova started about 3 hr after the commencement of ovulation or about 1\m=.\5 hr after the first ovum passed into the Fallopian tube; virtually all the ova were penetrated in the next 4 hr. In the females mated during or several hours after ovula- tion, sperm penetration occurred between 3 and 6 hr after coitus. The experiments in which spermatozoa were deposited artificially in the uteri of females shortly after ovulation, demonstrated that the sperma- tozoa recovered from the uterus of other females penetrated ova significantly faster than epididymal spermatozoa. The uterine sperma- tozoa deposited about the ova in vitro were also able to penetrate the ova more quickly than epididymal spermatozoa. The whole process of sperm penetration through the zona pellucida was observed on one occasion. This particular observation showed that: (1) the acrosome (at least, the outer acrosome membrane) of the fertilizing spermatozoon was absent before the spermatozoon started to penetrate the zona pellucida; (2) the direction of the passage of the spermatozoon was not vertical, but at an angle to the surface of the zona pellucida; (3) the time required for the sperm head to traverse the zona pellucida and the perivitelline space was 3 to 4 min and 1 to 2 sec, respectively; and (4) the head of the spermatozoon lay flat on the vitelline surface and sank into the vitellus without lively movements of the sperm flagellum.