1.Klinefelter's Syndrome.
Moon Sik PARK ; Young Il CHA ; Ki Bong PARK
Korean Journal of Urology 1969;10(4):177-181
Additional two cases of Klinefelter's syndrome with a literatural review was presented Two cases were revealed characteristics of Klinefelter's syndrome such as small testes, hyalinization of seminiferous tubules, azoospermia, increased FSH, normal 17-ketogteroid and positive sex chromatin. One case was associated with left inguinal crytorchidism.
Azoospermia
;
Hyalin
;
Klinefelter Syndrome*
;
Seminiferous Tubules
;
Sex Chromatin
;
Testis
2.Morphological Quantitative Study on Leydig Cell: Effect of Aging.
Korean Journal of Urology 1983;24(4):549-553
For the study of the effects of aging on testis, the volumes of testis and Leydig cells, young and old aged rats were sacrificed. Twenty eight testes from the young aged rats were used as the normal control. Ten testes showing the atrophic changes and sixteen not-atrophied testes of the old rats were used. After measurements of the volume and weight of the testes they were fixed in Bouin's solution and their sections were stained by Masson's trichrome. The Leydig cells appearing at the graticuels attached to eye-piece of the light microscope were calculated under one hundred magnification. The findings were summarized as follow: 1. The atrophied testes showed degenerative changes in the seminiferous tubules and had the slightly increased amount of the interstitium in comparison with the control. 2. The weight and volume of the normal control testes were 1.24gm and 1.19ml, respectively, and the proportion and the volume of Leydig cells of it were 3.78% and 0.045ml, respectively. 3. The atrophied testis of the old aged rats showed decreased weight and volume, 0.41gm and 0.57ml, but the proportion of Leydig cells was 9.15%, and the volume of the Leydig cells 0.052ml. 4. The weight and volume of the not-atrophied testis of the old aged rats were 1.73gm and 1.71ml, respectively. The proportion and volume of Leydig cells, however, were 3.04% and 0.052ml.
Aging*
;
Animals
;
Leydig Cells
;
Male
;
Rats
;
Seminiferous Tubules
;
Testis
3.An Experimental Study on the Effects of X-ray Irradiation and Hyperthermia on the Rat Testis.
Journal of the Korean Society for Therapeutic Radiology 1990;8(1):17-28
The effects of both hyperthermia alone and X-ray irradiation combined with hyperthermia on rat testis have been investigated. The histological changes were observed on 15 and 30 days after treatment. There was no histological change of rat testis by hyperthermia alone. The earliest change by x-ray irradiation was the degeneration of the spermatogonia of the seminiferous tubule, which was appeared in 2 gy group. Necrosis of the spermatogonia was severe in 6 gy group and complete atrophy was developed in 8 gy group. With increased dose of radiation, the degrees of changes of tubules was increased. In combined group of X-ray irradiation and hyperthermia, the histological change of the seminiferous tubule was more severe than X-ray alone group. Necrosis and atrophy of the spermatogonia were appeared in 2 gy and complete atrophy of spermatogonia was seen in 6 gy group. Thermal enhancement ratio (calculated at the complete atrophy of the spermatogonia) was 1.3 in this experiment. There was no difference in observation time inverval between 15 and 30 days after each treatment in all groups.
Animals
;
Atrophy
;
Fever*
;
Necrosis
;
Rats*
;
Seminiferous Tubules
;
Spermatogonia
;
Testis*
4.A Case of Cystic Ectasia of the Rete Testis.
Yun Seob SONG ; Tae Sung JUNG ; Seung Hwan DOO ; Won Jae YANG ; Dong Hwa LEE ; Seong Sook HONG
Korean Journal of Andrology 2012;30(1):90-91
The seminiferous tubules merge and connect with the tubuli recti that form the spaces known as the rete testis. Cystic ectasia of the rete testis is a rare benign testicular lesion. We report the cystic ectasia of the rete testis in a 66-year-old man.
Aged
;
Dilatation, Pathologic
;
Humans
;
Rete Testis
;
Seminiferous Tubules
;
Testis
5.Quantitative Analysis of the Seminiferous Epithelium in Human Testis.
Korean Journal of Urology 1986;27(4):511-517
Number of germ cells in the seminiferous epithelium was analyzed quantitatively in testicular biopsy specimens of 23 patients without ductal obstruction and of 4 patients with ductal obstruction. Roth number of mature spermatids within each cross-section of seminiferous tubule and number of atrophic tubule were counted in biopsy specimens. Results were expressed as cell number of mature spermatids per seminiferous tubule and percentage of atrophic tubules. A significant correlation was demonstrated between sperm density and mature spermatid counts. Patients with sperm counts of less than 40 x l0(6)/ml had mature spermatids counts of less than 25 per seminiferous tubule. Coefficients of correlation between mature spermatid count and percentage of atrophic tubules were higher than those of correlation between sperm counts and percentage of atrophic tubules. In asoospermrc patients with epididymal obstruction, sperm count after corrective surgery could be predicted correctly by this quantitative analysis technique of testicular biopsy specimens and partial obstruction of anastomotic site of seminal tract could be proved in oligozoospermic patients after corrective surgery.
Biopsy
;
Cell Count
;
Germ Cells
;
Humans*
;
Seminiferous Epithelium*
;
Seminiferous Tubules
;
Sperm Count
;
Spermatids
;
Spermatozoa
;
Testis*
6.Recent development in ectopic reconstitution of seminiferous tubules.
Ping LIU ; Zheng LI ; Juan-Jie BO
National Journal of Andrology 2010;16(10):928-932
The testicular development and spermatogenesis of mammalians involve complex processes of cell migration, proliferation and differentiation and cell-cell interaction. In spite of extensive researches, many relevant aspects remain unclear. One of the impediments in the studies of testicular development and spermatogenesis of mammalians is the lack of a suitable model. In the last few years, two valuable models were developed for the study of mammalian spermatogenesis: testis tissue from immature animals transplanted ectopically into immunodeficient mice that could survive and produce functional spermatids, and isolated testis cells able to organize and rearrange into seminiferous cords that subsequently undergo complete spermatogenesis. This article presents an update and the applications and prospects of these two methods.
Animals
;
Cell Culture Techniques
;
Humans
;
Male
;
Mice
;
Seminiferous Tubules
;
transplantation
;
Spermatogenesis
7.Testicular Biopsy: Comparison of Open Surgical and Percutaneous Needle Biopsy Techniques.
Sang Kon LEE ; Hyeon Hoe KIM ; Hee Yong LEE
Korean Journal of Urology 1985;26(4):327-330
Testicular biopsy has been known as very useful diagnostic procedure for the male infertility. For the past 9 months percutaneous testicular biopsy procedures were attempted on 64 patients with azoospermia or atrophic testis using a new Tru-Cut biopsy needle. In addition surgical testicular open biopsy procedure on one side and percutaneous testicular needle biopsy procedure on the other side were performed in comparison with two techniques. Biopsy specimens were fixed in Bouin solution. They were stained and histologically examined. Results were summarized as follows: Numbers of seminiferous tubules obtained by needle biopsy technique were found to be fewer than that of the tubules obtained by open biopsy technique. But diagnostic accuracy was not compromised by the needle biopsy technique. There was no bleeding either from the testis or scrotum, no extusion of testicular tissue from the puncuate site. In conclusion percutaneous testicular biopsy using Tru-Cut biopsy needle has been proved to be simple, time saving, less expensive and accurate method for testicular biopsy.
Azoospermia
;
Biopsy*
;
Biopsy, Needle*
;
Hemorrhage
;
Humans
;
Infertility
;
Infertility, Male
;
Male
;
Needles*
;
Scrotum
;
Seminiferous Tubules
;
Testis
8.Klinefelter's Syndrome.
Hyung Ryoul HUR ; Byoung Yoon RIM ; Bang Ok CHUN
Korean Journal of Urology 1970;11(3):157-161
A study was made on the two cases of Klinefelter's Syndrome with review of literature. Two cases revealed findings of characteristics of Kiinefelter's Syndrome such as small testes, atrophy of seminiferous tubules, azoospermia, increased urinary gonadotropin, decreased urinary 17 Ketosteroid, positive Sex Chromatin, gynecomstia and impotence.
Atrophy
;
Azoospermia
;
Erectile Dysfunction
;
Gonadotropins
;
Klinefelter Syndrome*
;
Male
;
Seminiferous Tubules
;
Sex Chromatin
;
Testis
9.A Case of 48XXXY Klinefelter's Syndrome.
Jse Pil CHO ; Dong Sun KIM ; Jae Heung CHO ; Se Kyung KIM
Korean Journal of Urology 1986;27(5):786-790
There are many variant forms in Klinefelter's syndrome which is characterized by azoospermia, gynecomastia, a variable degree of enuchoidism, elevated urinary gonadotropins, atrophic testis and hyalinization of the seminiferous tubules. Among these, 48XXXY from is known as rare variants of Klinefelter's syndrome which had been reported about 50 cases. 48 XXXY Klinefelter's syndrome is composed of more severe physical abnormality and more multiple symptom and signs than classic Klinefelter's syndrome. We have reported a case of 48 XXXY Klinefelter's syndrome associated with ophthalmic problems and mild mental retardation in 20 year old Korean male.
Azoospermia
;
Gonadotropins
;
Gynecomastia
;
Humans
;
Hyalin
;
Intellectual Disability
;
Klinefelter Syndrome*
;
Male
;
Seminiferous Tubules
;
Testis
;
Young Adult
10.Transcriptional regulatory networks underlying the reprogramming of spermatogonial stem cells to multipotent stem cells.
Hoe Su JEONG ; Jinhyuk BHIN ; Hyung Joon KIM ; Daehee HWANG ; Dong Ryul LEE ; Kye Seong KIM
Experimental & Molecular Medicine 2017;49(4):e315-
Spermatogonial stem cells (SSCs) are germline stem cells located along the basement membrane of seminiferous tubules in testes. Recently, SSCs were shown to be reprogrammed into multipotent SSCs (mSSCs). However, both the key factors and biological networks underlying this reprogramming remain elusive. Here, we present transcriptional regulatory networks (TRNs) that control cellular processes related to the SSC-to-mSSC reprogramming. Previously, we established intermediate SSCs (iSSCs) undergoing the transition to mSSCs and generated gene expression profiles of SSCs, iSSCs and mSSCs. By comparing these profiles, we identified 2643 genes that were up-regulated during the reprogramming process and 15 key transcription factors (TFs) that regulate these genes. Using the TF-target relationships, we developed TRNs describing how these TFs regulate three pluripotency-related processes (cell proliferation, stem cell maintenance and epigenetic regulation) during the reprogramming. The TRNs showed that 4 of the 15 TFs (Oct4/Pou5f1, Cux1, Zfp143 and E2f4) regulated cell proliferation during the early stages of reprogramming, whereas 11 TFs (Oct4/Pou5f1, Foxm1, Cux1, Zfp143, Trp53, E2f4, Esrrb, Nfyb, Nanog, Sox2 and Klf4) regulated the three pluripotency-related processes during the late stages of reprogramming. Our TRNs provide a model for the temporally coordinated transcriptional regulation of pluripotency-related processes during the SSC-to-mSSC reprogramming, which can be further tested in detailed functional studies.
Basement Membrane
;
Cell Proliferation
;
Epigenomics
;
Multipotent Stem Cells*
;
Seminiferous Tubules
;
Stem Cells*
;
Testis
;
Transcription Factors
;
Transcriptome