On the Function of the Interstitium of the Testis

1949 ◽  
Vol s3-90 (11) ◽  
pp. 265-280
Author(s):  
A. J. MARSHALL

1. An investigation of the seasonal cycle of the interstitium of the testes of birds, based on sixty-four individuals of varying age, has been carried out on the fulmar petrel, Fulmaris glacialis (L.). 2. The following cells (see diagram, p. 268) occur: (i) Fibroblasts of the sheaths of tubules, blood-vessels, and of groups of Leydig cells. (ii) Pigment cells. (iii) Juvenile Leydig cells (generally containing lipoid droplets). (iv) Lipoid Leydig cells. (v) Fuchsinophil Leydig cells. (vi) Areolar connective-tissue cells. 3. In the young bird the juvenile cell develops into the lipoid Leydig cell at a time when the testis-tubules also indicate approaching sexual maturity. In the adult, the interstitium generally consists for the most part of lipoid Leydig cells. These exhibit mitochondria when the soluble lipoids are removed by embedding in wax. At the height of spermatogenesis, and at the beginning of epithelial breakdown and tubule-regression, most of the Leydig cells have lost much of their lipoids and some of them exhibit increasing amounts of fuchsinophil substances, as described by Benoit. A fuchsinophil cell thus appears. 4. The Lipoid cell at all seasons shows a positive Schultz reaction (for cholesterol), which corresponds in intensity to the amount of sudanophil material present. It has not been possible to demonstrate cholesterol in the fuchsinophil cell. 5. At the time when the tubules are at their maximum diameter and their degeneration is under way, mitochondria are at the greatest abundance in the Leydig cell. At this period a new generation of Leydig cells arises in the interstitium. These cells quickly become meagrely sudanophil and resemble the sudanophil juvenile cells of the immature bird. They are Schultz positive. The tubules collapse; the new Leydig generation fills the empty interstitium. They exhibit profuse mitochondria, gain in lipoid content and so the interstitium is regenerated. 6. The exhausted tubules undergo a fatty metamorphosis at the time of their collapse; at the period when the interstitium has little lipoid the tubules are full of it. Beneath this fat (also Schultz positive) arises a new tubule-epithelium. The tubules as well as the interstitium are regenerated while the young of the next generation are still in the nests. An anatomical basis for an internal physiological rhythm may thus have been shown. 7. The new interstitial cells are already heavily lipoidal and the new tubule epithelium contains spermatogonia when the petrels move seaward away from the breeding cliffs in the autumn. They return to the breeding area in November and December. Thus testis regeneration, and movement both away from and back to the breeding area, occurs while the days are getting shorter. 8. From the time the birds appear on the breeding cliffs (and apparently since the autumn) there is an increase in lipoid cells along with heightened sexuality as revealed by the ripening tubule-products. These supplementary lipoid Leydig cells seem to develop from the small non-sudanophil areolar connective-tissue cells which are prominent in the adult interstitium. 9. Whilst it is not denied that the fuchsinophil cell (‘secretory cell’ of Sluiter and van Oordt) may have an endocrine function, the present results suggest that the lipoid Leydig cell is the primary secretory component of the avian testis. When the interstitium, after reproduction, passes once more to a lipoidal phase, it is not losing its secretory function as Sluiter and van Oordt infer, but is regenerating in readiness for the next season's breeding activities.

2021 ◽  
Vol 12 ◽  
Author(s):  
Dijana Z. Marinkovic ◽  
Marija L. J. Medar ◽  
Alisa P. Becin ◽  
Silvana A. Andric ◽  
Tatjana S. Kostic

The factors influencing Leydig cell maturity and the acquisition of functional capacity are incompletely defined. Here we analyzed the constant light (LL) influence on Leydig cells’ endocrine function during reproductive maturation. Rats were exposed to LL from P21 to P90. Data were collected at juvenile (P35), peri/pubertal (P42, P49), and adult (P90) stages of life. The results proved the effect of LL on rats’ physiology by changing of bimodal voluntary activity pattern into free-running. Additionally, the peripheral clock in Leydig cells changed in LL condition, indicating disturbed rhythm: the positive element (Bmal1) increased in pre-/pubertal but decreased in the adult period, while negative elements (Per2 and Reverba) were increased. The effects of LL were most prominent in puberty: pituitary genes encoding gonadotropic hormones (Cga, Lhb, Fshb) decreased; serum corticosterone increased, while serum androgens and mass of testicular and sex accessory organs reduced; markers of Leydig cells maturity/differentiation (Insl3, Lhcgr) and steroidogenesis-related genes (Scarb1, Star, Cyp11a1, Cyp17a1) decreased; the steroidogenic and energetic capacity of the Leydig cell mitochondria decreased; the mtDNA copy number reduced, and mitochondrial dynamics markers changed: fusion decreased (Opa1 and Mfn2), and mitophagy increased (Pink1). In adults, the negative effect of LL on mitochondrial function and steroidogenic capacity persists in adult Leydig cells while other parameters reached control values. Altogether, the results indicate that LL slows down Leydig cells’ maturation by reducing the endocrine and energy capacity of cells leading to the delay of reproductive development.


2020 ◽  
Vol 27 (12) ◽  
pp. 1246-1252
Author(s):  
Paolo Facondo ◽  
Andrea Delbarba ◽  
Filippo Maffezzoni ◽  
Carlo Cappelli ◽  
Alberto Ferlin

This article reviews the role of INSL3 as biomarker of Leydig cell function and its systemic action in testis-bone-skeletal muscle crosstalk in adult men. Insulin-like factor 3 (INSL3) is a peptide hormone secreted constitutively in a differentiation-dependent mode by testicular Leydig cells. Besides the role for the testicular descent, this hormone has endocrine anabolic functions on the bone-skeletal muscle unit. INSL3 levels are low in many conditions of undifferentiated or altered Leydig cell status, however the potential clinical utility of INSL3 measurement is not yet well defined. INSL3 levels are modulated by the long-term cytotropic effect of the hypothalamicpituitary- gonadal axis, unlike testosterone that is acutely sensitive to the stimulus by luteinizing hormone (LH). INSL3 directly depends on the number and differentiation state of Leydig cells and therefore it represents the ideal marker of Leydig cell function. This hormone is more sensitive than testosterone to Leydig cell impairment, and the reduction of INSL3 in adult men can precociously detect an endocrine testicular dysfunction. Low INSL3 levels could cause or contribute to some symptoms and signs of male hypogonadism, above all sarcopenia and osteoporosis. The measurement provided suggested that the measurement of INSL3 levels should be considered in the clinical management of male hypogonadism and in the evaluation of testicular endocrine function. The monitoring of INSL3 levels could allow an early detection of Leydig cell damage, even when testosterone levels are still in the normal range.


Endocrinology ◽  
2010 ◽  
Vol 151 (6) ◽  
pp. 2898-2910 ◽  
Author(s):  
Joachim Wistuba ◽  
C. Marc Luetjens ◽  
Jan-Bernd Stukenborg ◽  
Andreas Poplinski ◽  
Steffi Werler ◽  
...  

Sex chromosome imbalance in males is linked to a supernumerary X chromosome, a condition resulting in Klinefelter syndrome (KS; 47, XXY). KS patients suffer from infertility, hypergonadotropic hypogonadism, and cognitive impairments. Mechanisms of KS pathophysiology are poorly understood and require further exploration using animal models. Therefore, we phenotypically characterized 41, XXY* mice of different ages, evaluated observed germ cell loss, studied X-inactivation, and focused on the previously postulated impaired Leydig cell maturation and function as a possible cause of the underandrogenization seen in KS. Xist methylation analysis revealed normal X-chromosome inactivation similar to that seen in females. Germ cell loss was found to be complete and to occur during the peripubertal phase. Significantly elevated FSH and LH levels were persistent in 41, XXY* mice of different ages. Although Leydig cell hyperplasia was prominent, isolated XXY* Leydig cells showed a mature mRNA expression profile and a significantly higher transcriptional activity compared with controls. Stimulation of XXY* Leydig cells in vitro by human chorionic gonadotropin indicated a mature LH receptor whose maximal response exceeded that of control Leydig cells. The hyperactivity of Leydig cells seen in XXY* mice suggests that the changes in the endocrine milieu observed in KS is not due to impaired Leydig cell function. We suggest that the embedding of Leydig cells into the changed testicular environment in 41 XXY* males as such influences their endocrine function.


2014 ◽  
Author(s):  
Laura O'Hara ◽  
Kerry McInnes ◽  
Ioannis Simitsidellis ◽  
Steph Morgan ◽  
Laura Milne ◽  
...  

Diabetes ◽  
1991 ◽  
Vol 40 (5) ◽  
pp. 605-611 ◽  
Author(s):  
P. Muona ◽  
J. Peltonen ◽  
S. Jaakkola ◽  
J. Uitto

2011 ◽  
Vol 25 (7) ◽  
pp. 1211-1222 ◽  
Author(s):  
Soichi Yamashita ◽  
Ping Tai ◽  
Jean Charron ◽  
CheMyong Ko ◽  
Mario Ascoli

1995 ◽  
Vol 14 (7) ◽  
pp. 562-572 ◽  
Author(s):  
DE Prentice ◽  
AW Meikle

This paper describes control of normal Leydig cell func tion and testosterone production. The macroscopic and histopathological appearances of spontaneous Leydig cell hyperplasias and tumors (LCT) in the rat are reviewed together with their incidence and hormonal status. Drugs which induce LCTs in chronic studies are discussed and include busereline, carbamazepine, cimetidine, finas teride, flutamide, gemfibrozil, histrelin, hydralazine, indomethacin, isradipine, lactitol, leuprolide, metronida zole, mesulergine, nafarelin, norprolac and vidarabine. The known mechanisms of LCT induction in the rat are reviewed together with other possible etiological factors. The incidence, clinical picture and etiological factors of LCTs in man are also surveyed. Hormone production in Leydig cells and LCTs in rats and man are compared. Differences between the two species are considered, par ticularly with regard to Leydig cell control mechanisms. The paper concludes that drug-induced LCTs in rats are most probably not predictive for man and their occurrence has little relevance in human safety assessment.


1947 ◽  
Vol s3-88 (2) ◽  
pp. 135-150
Author(s):  
J. W. SLUITER ◽  
G. J. VAN OORDT

1. The relative volumes of the testes and their components of 31 cockerels, 2-200 days old, were calculated and compared with the size of their increasing head appendages (Text-figs. 1a-d, 2); in addition, the effect of gestyl-administration on testes of cockerels of this age was investigated. 2. Several types of interstitial testis-cells could be distinguished morphologically and physiologically (Text-figs. 3-6 and Pl. 1); these cell-types were studied with different techniques and counted separately. 3. The main types of the interstitial cells are: (a) Lipoid cells, totally packed with lipoid globules. These cells, which are considered by many authors as fully developed Leydig cells, are not directly connected with the production of the male sex hormone; perhaps they have a secondary function in this respect, as cholesterolderivatives are stored in these cells (Pl. 1, Text-fig. 3a). (b) Secretory cells, characterized by the absence of lipoid vacuoles and the presence of numerous granular and filamentous mitochondria. These secretory cells, which produce the male sex hormone, can be divided into secretory cells A (Text-fig. 6a) without, and secretory cells B with, one large vacuole (Text-figs. 6b, 6c, 6d). 4. A considerable and partly intercellular storage of lipoids may take place at any age in the intertubular connective tissue (Text-figs. 3-4 and Pl. 1). 5. The number of the lipoid cells depends on the nutritive conditions of the animal and the development of its testes (Text-fig. 7). 6. In older cockerels most of the glandular cells lose their secretory function and pass over into lipoid storing cells. 7. Therefore we agree with Benoit, when he denies the occurrence of a ‘secretion de luxe’, but we cannot accept the presence of a ‘parenchyme de luxe’ in the testes of older cockerels.


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