Showing papers in "Reviews of Reproduction in 1997"

Reactive oxygen species and sperm physiology

Abstract: Although high concentrations of reactive oxygen species (ROS) cause sperm pathology (ATP depletion leading to insufficient axonemal phosphorylation, lipid peroxidation and loss of motility and viability), recent evidence demonstrates that low and controlled concentrations of these ROS play an important role in sperm physiology. Reactive oxygen species, such as the superoxide anion, hydrogen peroxide and nitric oxide, induce sperm hyperactivation, capacitation or the acrosome reaction in vitro. The ROS involved in these processes may vary depending on experimental conditions, but all the evidence converges to describe these events as ‘oxidative’ or ‘redox regulated’. Human sperm capacitation and acrosome reaction are associated with extracellular production of a superoxide anion that is thought to originate from a membrane ‘oxidase’. The enzymes responsible for tyrosine phosphorylation‐dephosphorylation of sperm proteins are possible targets for ROS since mild oxidative conditions cause increases in protein tyrosine phosphorylation and acrosome reaction. The lipid peroxidation resulting from low concentrations of ROS promotes binding to the zona pellucida and may trigger the release of unesterified fatty acids from the sperm plasma membrane. The fine balance between ROS production and scavenging, as well as the right timing and site for ROS production are of paramount importance for acquisition of fertilizing ability.

Fetal undernutrition and disease in later life

Abstract: Recent findings suggest that coronary heart disease and stroke, and the associated conditions, hypertension and non-insulin dependent diabetes, originate through impaired growth and development during fetal life and infancy. These diseases may be consequences of 'programming', whereby a stimulus or insult at a critical, sensitive period of early life results in long-term changes in physiology or metabolism. Animal studies provide many examples of programming, which occurs because the systems and organs of the body mature during periods of rapid growth in fetal life and infancy. There are critical windows of time during which maturation must be achieved; and failure of maturation is largely irrecoverable.

Neuroendocrine regulation of gonadotrophin II release and gonadal growth in the goldfish, Carassius auratus.

Abstract: The goldfish, a member of the carp family, is a widely used model for reproductive neuroendocrine studies of economically important fish. The two gonadotrophin (GTH) molecules released from the fish anterior pituitary, GTH-I and GTH-II, are structurally similar to tetrapod FSH and LH, respectively. Gonadotrophin II is the best studied, and in goldfish stimulates gonadal growth and steroidogenesis, ovulation and sperm release. Growth hormone also has gonadotrophic actions in fish which enhance gonadal steroidogenesis. The principal stimulatory and inhibitory systems regulating GTH-II release are the gonadotrophin-releasing hormone (GnRH) and dopamine neurones in the preoptic-hypothalamic region. In goldfish there are two native GnRH forms, salmon GnRH and chicken GnRH-I; both stimulate GTH-II release but use different signal transduction pathways. In contrast to mammals, teleost fish do not have a median eminence and the GTH-II cells are thus directly innervated by neurones producing GnRH, dopamine and other stimulatory neurohormones. For most of these factors, the ability to stimulate GTH-II release varies seasonally. The amino acid neurotransmitter, gamma-aminobutyric acid, has the most prominent stimulatory actions which enhance GnRH release and inhibit dopamine turnover in the hypothalamo-pituitary complex. Neuropeptide Y stimulates GTH-II release by a combined direct action on the gonadotroph and also by enhancing GnRH release. Positive and negative sex steroid feedback mechanisms act concurrently to regulate GTH-II release in adults of both sexes. The principal site of positive feedback is the GTH-II cell where testosterone and oestradiol potentiate GnRH-stimulated GTH-II release. Negative feedback by sex steroids involves activation of inhibitory dopamine neurones, thus maintaining tight control over circulating GTH-II concentrations.

Adhesion molecules in implantation.

Abstract: At implantation, trophectoderm attaches to the apical uterine luminal epithelial cell surface. Molecular anatomy studies in humans and mice, and data from experimental models have identified several adhesion molecules that could take part in this process: integrins of the alpha v family, trophinin, CD44, cad-11, the H type I and Lewis y oligosaccharides and heparan sulfate. The endometrial cell surface mucin MUC1 may play a role in both steric inhibition of attachment and selective glycan display. After attachment, interstitial trophoblast invasion occurs requiring a new repertoire of adhesive interactions with maternal extracellular matrix as well as stromal and vascular cell populations. Human anchorage sites contain columns of cytotrophoblasts in which self-attachment gives way progressively to adhesion to extracellular matrix and then interstitial migration. The beta 1 integrins are important during these later stages of implantation and placentation.

Ovarian follicular dominance: the role of intraovarian growth factors and novel proteins

Abstract: Folliculogenesis is associated with the development of a group of follicles at various stages of maturation from which a species-specific number of follicles are selected for continued growth. These selected follicles, after being exposed to the requisite hormonal environment, ovulate in response to the preovulatory gonadotrophin surge. Follicular dominance is the mechanism by which the selected follicle(s) undergoes rapid development in an environment where growth and development of other follicles, recruited at a similar time, are suppressed. These processes are controlled by the interaction of endocrine signals and locally produced ovarian growth fac- tors. The response of the two major follicular cell types, granulosa and theca cells, to gonado- trophins is regulated by the local production of growth factors. Mechanisms controlling growth factor action occupy a central role in the regulation of folliculogenesis. In this review, we highlight the influence of the extracellular matrix in this process by describing its involve- ment in regulating the activity of components of the insulin-like growth factor system, trans- forming growth factor β superfamily, fibroblast growth factors and the epidermal growth factor/transforming growth factor α family. In addition, some recent studies on the role of pro- tein factors produced by the dominant follicle in maintaining dominance and inhibiting the growth of subordinate follicles are described.

Three-dimensional structure of the zona pellucida.

Abstract: The zona pellucida is the extracellular coat that surrounds the mammalian oocyte. It forms a spherical shell of remarkably uniform thickness (5‐10 µm in eutherian mammals). The mouse is currently the largest source of data on the zona pellucida and this review is built largely on these data. The zona pellucida is composed of three proteins in both mice and humans: ZP1, ZP2 and ZP3. These proteins are glycosylated and, in mice, have mature relative molecular masses of 200 000, 120 000 and 83 000, respectively. ZP1 is a dimer of two apparently identical subunits. All three mouse proteins have been sequenced and possess transmembrane domains at their C-terminal ends coupled with furin cleavage sites immediately upstream. Sequence data have been used to provide an accurate assessment of the mole ratios of the three proteins. The ratio of ZP2:ZP3 is close to 1:1, whereas ZP1 is approximately 9% of the combined mole amounts of ZP2 and ZP3. Ultrastructural evidence suggests that the mouse zona pellucida is composed of filaments constructed by head-to-tail association of globular proteins. The coordinate synthesis of the three zona pellucida proteins coupled with the near 1:1 stoichiometry of ZP2 and ZP3 is consistent with a model in which ZP2‐ZP3 heterodimers are the basic repeating units of the filament, with cross-linking of filaments by dimeric ZP1. This model is also consistent with data from ZP2 and ZP3 gene knockout and antisense experiments. However, the structure remains unproven. The small amount of ZP1 relative to ZP2 and ZP3 may have important implications for the distribution of ZP1 cross-links, since the number of crosslinking sites potentially exceeds the number of ZP1 dimer molecules by a considerable margin. The evidence that ZP1, ZP2 and ZP3 are all synthesized via a membrane-bound step is discussed and two models are proposed for the assembly of the zona pellucida. The cortical reaction and its effect on the zona pellucida are examined in detail. It is shown that the amount of material released by cortical granules could be of the order of 30% by mass of ZP1, and that if this material was distributed predominantly on the inner face of the zona pellucida, its local concentration could approach that of ZP1. A model in which the zona block to polyspermy is caused by direct titration of zona pellucida binding sites is suggested as an alternative to the explanation that relies on enzyme cleavage of ZP2 to ZP2

Reproductive biology of seals

Abstract: The reproductive biology of seals is fascinating in many aspects. As in most mammals, the time of onset of puberty in seals is variable. Once sexually mature, most but not all seals are seasonally mono-oestrous, with highly synchronized breeding seasons. They have evolved as either terrestrial or aquatic copulators, although a few species mate in a variety of habitats. Their mating strategies are diverse, ranging from serial monogamy to extreme polygyny. Gestation in seals is characterized by an embryonic diapause, which is obligate in most species. Reactivation of the blastocyst is followed by a placental gestation. All species of seal require a terrestrial (including ice floes) habitat for parturition. Lactation differs between the two seal families: phocid seals have an intense period of maternal investment, during which the mothers fast; otariid seals have a prolonged lactation during which intense bouts of suckling are interspersed by days of separation from their pups while the mother forages at sea. Although the anatomy and functional morphology of seals has been well described, less is known of the endocrinology of reproduction. This is due mainly to the logistical difficulties that researchers experience in collecting serial samples from a species that is relatively difficult to handle. This article reviews the basic anatomy and physiology, and our current understanding of the comparative aspects of reproduction in seals. Reproductive behaviours as well as the influences of environmental factors, such as photoperiod, nutrition and xenobiotics, are also discussed.

The human sperm centrosome is responsible for normal syngamy and early embryonic development

Abstract: As early as 1887, it was postulated that the mature oocyte possesses all of the elements necessary for embryonic development with the exception of an active division centre, and that the spermatozoon contains such a centre, but lacks the substrate in which to operate. This division centre is called the centrosome. The precise definition of this structure is still a subject for debate. It consists of two centrioles in a perpendicular arrangement and pericentriolar material, and is considered to be responsible for nucleation of microtubules and the formation of the mitotic spindle. There is a paternal pattern of inheritance of the centrosome in humans; thus, human oocytes lack centrioles but the spermatozoa carry two. At gamete fusion the sperm tail is incorporated into the ooplasm, and the centriolar region forms the sperm aster while the sperm head is decondensing; this aster acts to guide the female pronucleus towards the male pronucleus. The centriole duplicates during the pronuclear stage, and at syngamy centrioles are found at opposite poles of the first cleavage. The centrosome has several implications for human infertility. It is possible that immotile or nonprogressively motile spermatozoa may possess centriolar abnormalities or an absence of centrioles. Similarly, antisperm antibodies against centrioles may be responsible for mitotic arrest. One way of solving this problem would be the use of donor centrosomes. To this end, we have assessed the ability of embryos injected with physically separated sperm segments (head only, head and tail separated or isolated tail) to develop normally. Fluorescent in situ hybridization revealed an almost universal mosaicism in these embryos, suggesting that physical disruption of the spermatozoa compromises the ability of the centrosome to function in the zygote. Thus far, centrosome donation with centriole-carrier flagellae obtained by this dissection method does not appear to be feasible.

Noradrenergic regulation of cyclic GnRH secretion

Abstract: The GnRH cells represent the final output neurones of an integrated neuronal network used by the brain to generate pulsatile LH secretion from the pituitary gland. Changes in LH secretion profile throughout the ovarian cycle, including the preovulatory LH surge, result principally from alterations in the output of this GnRH network and it has been a key goal of many neurobiologists to elucidate the components and nature of this network. This review documents recent progress in understanding the role of noradrenaline within the GnRH network and highlights and explains its 'enabling' or permissive characteristics. Network behaviour analysis suggests that noradrenaline should be considered as a permissive agent promoting high output states of the GnRH network. On the basis of recent molecular and neuroanatomical data, it is proposed that oestrogen influences brainstem noradrenergic neurones specifically within the nucleus tractus solitarius to facilitate synaptic transmission within the GnRH network. In this manner, noradrenaline is likely to play a role in bringing about the increased GnRH messenger RNA expression and secretion necessary for ovulation.

Central oxytocin and reproductive behaviours

Abstract: Oxytocin is a neurohypophyseal hormone that has long been associated with uterine contraction during parturition and milk ejection during nursing. Recent studies have suggested that oxytocin is also a neurotransmitter that has central effects important for reproduction, including the initiation of parental and sexual behaviours. This review describes oxytocin pathways in the brain and examines their regulation by gonadal steroids. Brain oxytocin receptors are remarkable for their plasticity and for striking species differences in their distribution. The molecular characterization of this receptor has provided several clues to the regulation of its expression. Comparative and transgenic studies suggest that central oxytocin release may influence reproductive behaviours, but the importance of these central effects depends on the pattern of expression of the receptor ‐ a pattern that is species-specific.

Placental 11 beta-hydroxysteroid dehydrogenase: barrier to maternal glucocorticoids

Abstract: During mammalian pregnancy, the circulating concentration of cortisol (in rodents, corticosterone) in the mother is much higher than that in the fetus. Since the placenta is the only barrier, apart from the uterus, between the mother and her fetus, this gradient in cortisol concentrations suggests that there is a placental barrier preventing maternal cortisol from crossing into the fetus. The intracellular enzyme 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) is an ideal candidate for this barrier because it interconverts cortisol and corticosterone to their inactive metabolites cortisone and 11-dehydrocorticosterone. Indeed, 11 beta-HSD enzyme is expressed in the placenta of humans and a range of other animal species. Moreover, it is well positioned to serve as the barrier since it is localized to the syncytiotrophoblast, the site of maternal-fetal exchange. Given that fetal exposure to excessive amounts of glucocorticoids leads to intrauterine growth retardation, it has been hypothesized that the physiological significance of this placental 11 beta-HSD barrier is to protect the fetus from adverse effects of maternal glucocorticoids.

Testicular leukocytes: what are they doing?

Abstract: Leukocytes, specifically macrophages, lymphocytes and mast cells, are found within the testes of most, if not all, mammals. In some species (for example, rats, mice and humans), the number of 'resident' testicular macrophages, in particular, is quite considerable. However, reproductive biologists are only beginning to explore the characteristics and possible biological significance of these cells. As in other tissues, the testicular leukocytes are involved in immunological surveillance, immunoregulation and tissue remodelling. They are implicated in the mechanisms that make the testis a particularly successful site for tissue transplantation in some experimental animals. Moreover, recent studies have demonstrated that the testicular macrophages have specific trophic effects on Leydig cell development and steroidogenesis. In turn, the development and functions of the testicular leukocyte population are clearly influenced by the testicular environment, and especially by the Leydig cells and Sertoli cells. These data indicate an important role for leukocytes in testicular homeostasis. Balanced against this beneficial role is the fact that these cells possess the potential to damage testicular function in conditions of immune activation, as their inflammatory and cytotoxic activities may disrupt the normal environment of the testis. The importance of the testicular leukocytes to normal and abnormal testicular function is evident. The challenge for future research is to define the details of this relationship.

In vitro culture of ovarian follicles

Abstract: This review offers a practically oriented introduction to follicle culture in vitro, focusing on mouse follicles, but with reference to other species. The main principles of follicle growth are addressed, including the constraints of tissue culture, methods of follicle isolation, and techniques for individual and collective culture of intact follicles. Culture systems that support a spherical or a non-spherical follicular structure in vitro are discussed in terms of follicular and oocyte development, and methods for assessing follicular function in vitro are presented. Oocyte development in most in vitro culture systems is currently suboptimal and the parallel development of oocytes and follicles is discussed, with a view to maintaining the competence of the oocyte. Finally, some potential future applications of follicle growth in vitro are suggested.

Preimplantation growth factor physiology.

Abstract: Development and differentiation of the eutherian zygote to a laminar blastocyst occur during the journey through the reproductive tract. In the absence of anatomical union, synchronization of embryonic and maternal physiologies must rely on diffusible signals to support and optimize developmental potential throughout this period of about 6 days. Discoveries of the activities of growth factors and their receptors in general biology during the late 1970s coincided with a recognition that they may be the means by which preimplantation embryos optimize their potential. Concurrently, application of the assisted reproductive techniques developed for animals to human infertility had achieved success with the birth of Louise Brown (Steptoe and Edwards, 1978). This event invigorated interest in embryo culture and, in particular, the roles of growth factors which were known to play regulatory roles in development in better understood non-mammalian developmental models such as amphibians, sea urchins and chickens (for comprehensive reviews see Schultz and Heyner, 1993; Kaye and Harvey, 1995; Pampfer and De Hertogh, 1996).

Environmental oestrogens - present understanding

Abstract: Three years ago it was hypothesized that the reported adverse changes in male reproductive health could be explained by exposure to compounds with oestrogenic (or other hormone disruptive) activity. Although this issue has been highly publicized, there has been little progress towards a realistic assessment of whether environmental oestrogens pose a health risk to humans. This article attempts to give a brief overview of the current status of knowledge concerning environmental oestrogens and highlights some of the difficulties associated with risk assessment. Compounds within several major groups of chemicals, including organochlorine pesticides, polychlorinated biphenyls, phenolic compounds and phthalate esters, have been identified as being weakly oestrogenic by in vitro and in vivo screening methods. Many of these compounds are widespread and persistent in the environment. They are likely to be present in the food chain, drinking water, plastics, household products and food packaging, although which is the most important route of human exposure is unclear. In addition to exposure to man-made chemicals, the consumption of plant-derived oestrogens in foodstuffs poses a potential risk to human health as phytoestrogens are more potent oestrogens and their intake by some infants is likely to be considerable.

Nuclear transfer and reprogramming.

Abstract: Nuclear transfer techniques for mammalian embryos have been developed in the last decade. Embryonic nuclei from advanced stages of preimplantation development can be fully reprogrammed and the totipotency is restored when nuclei are transferred into ooplasts. Transfer of nuclei after gene expression from the embryonic genome has started does not appear to restrict the reprogramming of these nuclei. The principles of nuclear transfer are outlined with respect to nuclear remodelling, nucleocytoplasmic interactions and effects of the cell cycle. However, the molecular mechanisms involved in reprogramming donor nuclei remain unknown. It is proposed that epigenetic DNA modification, such as DNA methylation that regulates gene expression, is related to the reprogramming of transplanted nuclei.

Biology of the relaxin-like factor (RLF)

Abstract: The relaxin-like factor (RLF) is a novel member of the insulin-IGF-relaxin family of hormones and growth factors. Also known as the Leydig cell insulin-like factor (Ley-I-L), this peptide and the mRNA encoding it appear to be expressed in very large quantities in the Leydig cells of the testis. However, it is also produced in the ovary of a number of species in both follicular theca cells and in the corpus luteum of the cycle and pregnancy. RLF gene transcripts have been identified at a much lower level of expression throughout the bovine female reproductive tract and also in the hypothalamus. Although data are limited, it would appear that RLF represents a new differentiation-related factor with specific functions linked to reproductive physiology in male and female mammals.

Models for male infertility: the t haplotypes

Abstract: The t haplotypes are variant alleles of genes in the proximal region of mouse Chromosome 17, linked together by four inversions. While females carrying two t haplotypes are fertile, males are sterile. Their spermatozoa exhibit severe motility defects and are unable to penetrate zona pellucida-free oocytes. Spermatozoa from males carrying one t haplotype (t/+) exhibit mild motility deficits and a delay in penetration of the zona-free oocyte. The inversions of the t haplotypes contain several genes that cause or contribute to male sterility, at least some of which can be identified by analysis of mice carrying Mus spretus-Mus domesticus recombinant Chromosomes 17. The t haplotypes specify a number of sperm biochemical abnormalities, but these have not been related directly to defects in fertilization. In t/+ males, spermatozoa not bearing the t haplotype are defective in fertilization compared with t-bearing spermatozoa. The mechanism causing this is likely to involve haploid gene expression confined to the t-bearing spermatids. Since many genes situated in the region of the t haplotypes have human homologues, an understanding of t haplotype sterility in mice is expected to contribute significantly to our knowledge of the genetic basis for human sperm dysfunction.

Roles of reactive oxygen species in the regulation of luteal function

Abstract: Ephemerality and prolongation of luteal function have been matters of great concern in reproduction for many years. However, their control mechanisms are very complex and differ among mammals. Recently, evidence has indicated that reactive oxygen species may play important roles in the regulation of luteal function. Reactive oxygen species are present in most somatic cells and are involved in apoptosis, or 'physiological cell death'. In the corpus luteum, reactive oxygen species also exert luteolytic effects as well as some paradoxical luteotrophic effects. This paper discusses the possible roles of reactive oxygen species in the control of luteal function.

Advances in understanding gonadotrophin-releasing hormone receptor structure and ligand interactions

Abstract: Gonadotrophin-releasing hormone (GnRH) is the central regulator of the reproductive system and its analogues are used widely in the treatment of diverse diseases. The GnRH receptor is a member of the large family of G-protein-coupled receptors (GPCRs) which have seven transmembrane domains. Knowledge of these receptors has assisted the development of molecular models of the GnRH receptor that allow prediction of its threedimensional configuration and the way GnRH binds and activates its receptor. Comparison with other GPCRs led to the discovery that Lys121 , in the third transmembrane domain, has a role in agonist binding. The history of GnRH structure‐activity studies has allowed the identification of an acidic residue in the third extracellular loop of the receptor that is required for binding of mammalian GnRH, while synthetic GnRH analogues have showed that Asn102 , in the second extracellular loop, may interact with the carboxy-terminus of GnRH. These residues can now be incorporated into the receptor models that are being used to design orally active non-peptide GnRH analogues for contraception and treatment of a variety of reproductive disorders.

HLA-G and pregnancy.

Abstract: Recent studies of the nonclassical HLA-G class I gene provide insight into its function(s) during pregnancy. The HLA-G gene can be transcribed in different isoforms resulting from alternative splicings and encoding membrane-bound and soluble proteins. These different mRNA species have been found in the various trophoblast cell subpopulations that constitute the maternofetal interface in the human placenta. The raising of antibodies to HLA-G has introduced new tools to determine in which types of trophoblast cells and in which other tissues these transcriptional isoforms are translated in functional proteins. The HLA-G gene exhibits a certain amount of polymorphism, the exon three that encodes the alpha 2 external domain showing the most extensive nucleotide variability. It remains to be determined whether the homozygosity of some HLA-G alleles constitutes a real disadvantage in terms of pregnancy or resistance to specific pathogens. Regarding the potential antigen-presenting function(s) of HLA-G, two isoforms are capable of binding an identical set of nonamer peptides derived from a variety of intracellular proteins. The ligand motif contains three anchor residues and is similar to that of classical HLA class I molecules. Experiments are being performed to identify the recognizing cells and to determine whether HLA-G induces a cytolytic (including anti-viral) T-cell response or in some other way represses natural killer-cell functions.

Regulatory mechanisms in acrosomal exocytosis.

Abstract: Acrosomal exocytosis occurs after the binding of the spermatozoon to the zona pellucida of the oocyte via specific receptors. We suggest that the zona pellucida binds to at least two different receptors in the plasma membrane. One (R) is a Gi-coupled receptor that activates phospholipase C beta 1. The other (TK) is a tyrosine kinase receptor coupled to phospholipase C gamma. Binding to R would regulate adenylyl cyclase leading to an increase in cyclic adenosine monophosphate and protein kinase A activation. The protein kinase A activates a voltage-dependent Ca2+ channel in the outer acrosomal membrane that releases Ca2+ from the interior of the acrosome to the cytosol. This is the first (I), relatively small, rise in intracellular Ca2+ which leads to activation of the phospholipase C gamma. The products of phosphatidyl-inositol bisphosphate hydrolysis by phospholipase C, diacylglycerol and inositol-trisphosphate lead to protein kinase C translocation to the plasma membrane and its activation. Protein kinase C opens a voltage-dependent Ca2+ channel (L) in the plasma membrane, leading to the second (II), higher, increase in intracellular Ca2+ leading to acrosomal exocytosis. Spermine, a physiological constituent of the seminal plasma regulates sperm acrosomal exocytosis by modulating intracellular Ca2+ binding sites and phospholipase C activity. Spermine is rapidly incorporated into the sperm cells during ejaculation and temporarily inhibits premature capacitation and acrosome reaction. During the passage of the spermatozoon through the female genital tract, there is a progressive depletion of spermine from spermatozoa, so that capacitation and consequently the acrosomal exocytosis take place at the appropriate time, when the spermatozoon reaches the vicinity of the egg.

Prolactin receptor subtypes: a possible mode of tissue specific regulation of prolactin function

Abstract: Prolactin mediates its effect on target cells through an interaction with membrane-anchored receptors. In the last decade, several subtypes of the receptor have been isolated from different species. This has generated a great deal of interest in the roles of the receptor subtypes and the possible divergent signalling pathways in mediating the pleiotropic effects of prolactin on target tissues. Our current knowledge of the signalling pathway of prolactin is derived mainly from the interaction of the hormone with one of its receptor subtypes (the long form) isolated from rats. In vitro expression studies have led to the identification of the regions within the long form prolactin receptor that are essential for the association of the tyrosine kinase Jak-2, and the phosphorylation events leading to activation of the prolactin responsive beta-casein promoter. To date, a specific target gene that may be activated after interaction of prolactin with the short form of the receptor has not been identified. However, the different receptor subtypes are present in the same cell type in vivo and their expression is hormone regulated, possibly through multiple promoters that control transcription of the prolactin receptor gene. Comparative studies suggest that the signalling pathways and the relevance of different receptor subtypes on prolactin function may vary between species.