ABSTRACT
The persistent Müllerian duct syndrome (PMDS) is characterized by the persistence of Müllerian derivatives, uterus and tubes, in otherwise normally virilized males. In a previous study, we showed that this syndrome is heterogeneous, with lack of production of anti-Müllerian hormone (AMH) by testicular tissue accounting for only some, AMH-negative, cases of this disorder. We have characterized the point mutation responsible for an AMH-negative PMDS in three siblings: a guanine to thymine transversion at position 2096 in the fifth exon changes a GAA triplet, coding for glutamic acid, to a TAA stop codon. The mutation could also be recognized, using the polymerase chain reaction, on RNA produced in trace amounts by a lymphoblastic cell line. The translation product, although undetectable in testicular tissue, could be visualized in culture medium of cells transfected with the mutant gene.
Subject(s)
Disorders of Sex Development/genetics , Glycoproteins , Growth Inhibitors/genetics , Testicular Hormones/genetics , Anti-Mullerian Hormone , Base Sequence , Blotting, Southern , Blotting, Western , Growth Inhibitors/deficiency , Humans , Male , Molecular Sequence Data , Mutation , Oligonucleotides/chemistry , Polymerase Chain Reaction , RNA, Messenger/genetics , Testicular Hormones/deficiency , Transcription, GeneticABSTRACT
Anti-Müllerian hormone (AMH), also called Müllerian-inhibiting substance or factor was measured by an interspecific enzyme-linked immunoassay in the serum of 218 normal children and adults of both sexes and in 110 boys with various developmental disorders. AMH levels were high [81.67 ng/ml +/- 7.44(SEM)] in normal males under 2 yr of age, fell progressively in older boys and, decreased sharply at puberty. Serum AMH was not detectable in adults or in females at any age, with very rare exceptions. AMH serum concentrations were significantly decreased in infants with disorders of sex differentiation, particularly testicular dysgenesis, and increased in patients with delayed puberty. In contrast, levels were not significantly affected by either cryptorchidism or chorionic gonadotropin stimulation. AMH shows promise as a marker of testicular function in infancy.
Subject(s)
Glycoproteins , Growth Inhibitors/blood , Testicular Hormones/blood , Testis/physiology , Adolescent , Anti-Mullerian Hormone , Biomarkers/blood , Child , Child, Preschool , Developmental Disabilities/blood , Enzyme-Linked Immunosorbent Assay , Female , Gonadal Dysgenesis/blood , Growth Inhibitors/physiology , Humans , Hypopituitarism/blood , Infant , Infant, Newborn , Male , Monitoring, Physiologic , Puberty, Delayed/blood , Sex Differentiation , Sexual Maturation , Testicular Hormones/physiologyABSTRACT
A rare form of male pseudohermaphroditism is characterized by the persistence of Müllerian derivatives in phenotypic males. To determine the etiology of this syndrome, we studied the expression of anti-Müllerian hormone (AMH) in six boys, including three brothers, with the persistent Müllerian duct syndrome. All except one presented with an inguinal hernia containing the Müllerian derivatives, and in two boys the hernial sac contained the contralateral testis. AMH was normally expressed in the testicular tissue of two patients, as shown by bioassay of anti-Müllerian activity and immunocytochemistry. The testicular tissue of the other patients had no detectable bioactive or immunoreactive AMH, yet they expressed AMH mRNA with a normal transcription initiation site and in the amount expected for their age. These results prove the heterogeneity of the persistent Müllerian duct syndrome and suggest that it may sometimes involve peripheral insensitivity to AMH.
Subject(s)
Disorders of Sex Development/etiology , Glycoproteins , Growth Inhibitors , Mullerian Ducts , Testicular Hormones/blood , Animals , Anti-Mullerian Hormone , Child, Preschool , Cryptorchidism/complications , Disorders of Sex Development/genetics , Disorders of Sex Development/physiopathology , Hernia, Inguinal/complications , Humans , Infant , Male , Rats , Syndrome , Testis/physiopathologyABSTRACT
Using immunochromatography on a polyclonal antibody, testicular anti-Müllerian hormone (AMH) was purified from homogenates of human fetal testicular tissue and used as an antigen for hybridoma production. Two IgM clones were obtained. Both recognized AMH on biopsies of human testicular tissue and one blocked its anti-Müllerian activity. This monoclonal antibody (MAb) exhibited a relatively high affinity for AMH, and was studied further. It is interspecific, recognizing AMH in other mammalian species. The study of this MAb in relation to an IgM MAb raised against bovine AMH (bAMH) indicates that both MAbs recognize different but related epitopes on bAMH.
Subject(s)
Antibodies, Monoclonal , Glycoproteins , Growth Inhibitors , Mullerian Ducts , Testicular Hormones/immunology , Anti-Mullerian Hormone , Antibodies, Monoclonal/immunology , Antibody Formation , Antigen-Antibody Reactions , Epitopes/analysis , Female , Fetus , Humans , Hybridomas/immunology , Immunoglobulin M/isolation & purification , Immunohistochemistry , Male , Pregnancy , Testicular Hormones/analysis , Testis/analysisABSTRACT
Monoclonal antibodies (Mabs) have been raised against purified bovine anti-Müllerian hormone (bAMH) in an effort to obtain nonzoospecific reagents. Although the majority of the resulting hybridomas resembled those obtained previously insofar as they recognized only bovine, ovine and caprine AMH, four others, all immunoglobulin Ms, were directed against an epitope shared with AMH of other species, namely rabbit, pig and cat. Both the zoospecific and the conserved epitopes were located close to the site required for biological activity. It is suggested that the similarity between the immunogenic characteristics of bovine, ovine and caprine AMH is in some way related to the fact that AMH in these species is disseminated in the blood stream and may produce freemartinism.
Subject(s)
Antibodies, Monoclonal , Epitopes/analysis , Glycoproteins , Growth Inhibitors , Testicular Hormones/analysis , Animals , Anti-Mullerian Hormone , Cattle , Female , Goats , Immunoenzyme Techniques , Male , Mice , Mice, Inbred BALB C , Sheep , Species Specificity , Testicular Hormones/immunology , Testis/cytologyABSTRACT
Anti-Müllerian hormone (AMH) has been detected by RIA in the follicular fluid of mature bovine ovaries and in incubation medium of bovine granulosa cells. Purification of AMH from two independent batches of follicular fluid was achieved with a yield of 11% and 15% respectively. Both ovarian and control testicular AMH produced near-complete regression of fetal rat Müllerian ducts exposed to it in culture at a final concentration of 200-300 mU/ml and were recognized by the same monoclonal and polyclonal antibodies. These findings indicate that adult mammalian granulosa cells are capable of producing immunoreactive and bioactive AMH at a rate apparently similar to that already demonstrated for mature Sertoli cells and add yet another item to the homologies reported between male and female somatic gonadal cells.
Subject(s)
Glycoproteins , Granulosa Cells/physiology , Growth Inhibitors , Sertoli Cells/physiology , Testicular Hormones/biosynthesis , Animals , Anti-Mullerian Hormone , Biological Assay , Cattle , Female , Fetus , Granulosa Cells/metabolism , Male , Mullerian Ducts/drug effects , Mullerian Ducts/physiology , Ovary/physiology , Radioimmunoassay , Rats , Sertoli Cells/metabolism , Testicular Hormones/isolation & purification , Testicular Hormones/pharmacologyABSTRACT
The origin of AMH responsible for Müllerian duct regression in bovine freemartins has been reinvestigated, using a sensitive RIA for this hormone. Between 50 and 80 days, Müllerian duct regression occurs simultaneously in males and freemartins. Both twins exhibited high and positively correlated serum AMH concentrations, whereas gonadal in-vitro production of AMH and biological anti-Müllerian activity were detectable at a low level only in 2 out of 13 freemartins. In the gonads of approximately half the freemartins after 80 days, seminiferous tubules differentiated and the gonads produced AMH, but the output was very low compared to that of the male twin. These data suggest that regression of Müllerian duct in freemartins is essentially mediated by AMH produced by the testes of the male twin.
Subject(s)
Freemartinism/embryology , Glycoproteins , Growth Inhibitors , Mullerian Ducts/physiology , Testicular Hormones/biosynthesis , Testis/embryology , Animals , Anti-Mullerian Hormone , Cattle , Culture Techniques , Female , Fetal Blood/analysis , Fetus/metabolism , Freemartinism/metabolism , Male , Ovary/embryology , Ovary/metabolism , Pregnancy , Radioimmunoassay , Testicular Hormones/blood , Testis/metabolism , TwinsABSTRACT
Two monoclonal antibodies have been used to set up a solid-phase RIA for bovine anti-Müllerian hormone (bAMH). One AMH unit is defined as the amount released by 1 g of bovine fetal testicular tissue during a 4 h incubation period. Calibration curves were prepared using aliquots of a standard 500 ml pool of incubation medium, containing 200 AMH mU/ml, diluted either in 50% pig testes incubation medium, 5% horse serum, 10% female calf fetal serum or pure female calf fetal serum. Linearization of the calibration curves was achieved through "logit-log" transformation, all four lines were parallel. Within and between-assay variability were less than 5%. The RIA is at least 600 times more sensitive than the bioassay for anti-Müllerian activity and can detect AMH in male and freemartin fetal serum.