Electron Microscopic Observations on Spinal Ganglion Cells of Rana pipiens after Injection of Malononitrile

Spinal ganglionic cells of Rana pipiens were studied with light and electron microscopes in normal animals and in animals which had received graded dosages of malononitrile intraperitoneally. After treatment no increase in the intensity of staining was noted in the Nissl substance when spinal ganglion cells were examined with the light microscope. The electron micrographs demonstrated the following in malononitrile-treated animals: 1. The cisternae of the endoplasmic reticulum composing the Nissl bodies appeared to fragment and lose their parallel orientation. 2. The microvesicular components of the Golgi complex appeared to increase in number, and the increase was apparently due to fragmentation of the membrane system of the Golgi complex. 3. The mitochondria enlarged and became pleomorphic, but displayed no alterations of internal structure. The morphological changes may be interpreted as reflections of biochemical alterations.     

Speciation in the Rana pipiens Complex

The long held view that leopard frogs (Rana pipiens complex)are a single widely distributed species is not correct. Fivesibling species are currently recognizable. These findings haveimportant implications on the use of leopard frogs in experimentalresearch.     

The ultimobranchial body in Rana pipiens

Summary Hypercalcemia was induced in male frogs by injection of Vitamin D₂ and maintaining animals in calcium chloride water. The fine structure of the Ultimobranchial gland was examined 3, 7 and 14 days after the initial injection. The initial response observed after the third day was a depletion of secretory granules in addition to an alteration of nuclear shape and cytoplasmic hypertrophy. After seven days secretory granule depletion continued and early cell types occurred which indicated an increase in mitotic activity. There was also a demonstrable increase in the amount of ergastoplasm and hypertrophy of the Golgi apparatus. On the fourteenth day, the height of the epithelium was markedly increased while the underlying vascular network was enlarged and more intimately associated with the secretory parenchyma. The homeostatic mechanisms of the Ultimobranchial gland appear to include both a rapid secretory response upon stimulation and a cellular renewal system to replace exhausted cells. This suggests that such a glandular system provides a mechanism to supply a rapidly expanding cell population to meet the demands of an excessive depletion of secretory materials. The response of this gland to hypercalcemia supports previous studies which suggest that the Ultimobranchial gland is the probable source of the hypocalcemic hormone, calcitonin.This project was supported in part by funds provided by the Department of Anatomical Sciences and National Institutes of Health, Grant No. AM-11795.     

Cytodifferentiation in the Rana pipiens oocyte

Summary In early diplotene frog oocytes incubated to illustrate thiamine pyrophosphatase (TPPase) activity, reaction product is uniformly distributed within the compartments of the endoplasmic reticulum and nuclear envelope as well as within the saccules and small vesicles comprising the dictyosomes. With continued oocyte development the reaction product becomes concentrated in localized regions of the dictyosome saccules. Eventually, the enzyme is no longer apparent within the endoplasmic reticulum, but is concentrated in the cisternae of the inner dictyosome saccules. The variations noted suggest that the enzyme is synthesized early in diplotene by the endoplasmic reticulum and is subsequently transported to the Golgi apparatus where it is consistently observed at later developmental stages. TPPase activity is also present in the Golgi apparatus of follicle and theca cells as well as in ovarian epithelial cells. The enzyme is also detected in micropinocytotic vesicles contained within the cells comprising the follicle envelope and in intercellular spaces of the follicle. Horseradish peroxidase injected into the coelomic cavity is transported via micropinocytotic vesicles into and through the cells comprising the follicle envelope and in intercellular spaces. The exogenous protein is not found even after a prolonged time period in early diplotene oocytes. The protein is, however, present in large spherical and tubular vesicles in the cortex of vitellogenic oocytes approximately 500 microns in diameter. The possible functional role of the enzyme TPPase during oogenesis is discussed.This investigation was supported by a research grant from the National Science Foundation (GB-8736).     

The ultimobranchial body in Rana pipiens

Summary Autoplastic transplants of ultimobranchial glands of male Rana pipiens were bilaterally or unilaterally placed in a homeotopic or heterotopic site. Serum calcium levels were maintained at normal values in bilateral autotransplants, while total ultimobranchialectomy resulted in hypercalcemia. Electron microscopy verified the viability and functional state of transplanted, denervated glands. During the periods of denervation, ergastoplasm and Golgi membranes exhibited hypertrophy which was reversed when unmyelinated nerves reappeared in the pericapillary space. Autotransplants under hypercalcemic conditions indicated that the process of secretion is primarily an intrinsic cellular activity and independant of innervation. The present evidence suggests that the sympathetic axons which innervate the parenchyma probably are inhibitory in nature and may allow depression of glandular functions during periods of hypercalcemia.The technical assistance of Mrs. Lilly Weeks is gratefully acknowledged. This project was supported by N. I. H. Grant No. AM-11795; The National Institutes of Arthritic and Metabolic Diseases.     

A study on hearing in frogs (Rana pipiens and Rana clamitans)

Zusammenfassung Die relative Reizschwellkurve für die Schallempfindung bei den Fröschen Rana clamitans und R. pipiens wurde in dem Frequenzbereich von 30–15000 Hz bestimmt. Die Kurve ist dieselbe für beide Geschlechter. Versuche zeigten, daß Schälle entweder inhibierend oder stimulierend auf die Atmungsbewegungen wirken können. Diese Wirkung wird nicht von der Frequenz oder der Intensität der Schälle bestimmt, sondern von dem physiologischen Zustand des Tieres.Die Latenzzeit zwischen Reiz und Effekt ist unabhängig von der Tonfrequenz, wird aber von den Intervallen zwischen aufeinanderfolgenden Reizen beeinflußt; sie wird kürzer, wenn die Intervalle verlängert werden.Dressurversuche mit 18 Tieren, unter Anwendung von Strafung durch elektrische Schläge und einem Dressurton von 300 Hz, ergaben positive Erfolge bei zwei Individuen von R. clamitans.

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Contribution No. 67 of the Department of Biology, Hamilton College, McMaster University, Hamilton, Ontario.     

Cell adhesion to extracellular matrix in normal Rana pipiens gastrulae and in arrested hybrid gastrulae Rana pipiens female X Rana esculenta male

Rana pipiens eggs fertilized by Rana esculenta sperm (ESC) hybrid embryos develop until gastrulation in control Rana pipiens embryos (PIP) and then show morphogenetic arrest. After arrest, ESC do not gastrulate but live for 5 days as blastula-like embryos. We studied the distribution of fibronectin (FN)-containing fibrils and integrin (INT) in PIP and ESC. There are many FN-fibrils in PIP organized in anastomosing networks radiating away from the center of individual cells and across intercellular boundaries. ESC have fewer fibrils compared to PIP. These fibrils are first located between cells in disorganized arrays. After arrest in ESC, when PIP are Stage 14 neurulae, many more FN-fibrils appear. INT-staining occurs in both embryos in similar patterns. In xenoplastic transplantations, we found that the extracellular matrix on the inner surface of the ESC blastocoel roof serves as a substratum for PIP cell migration. In an in vitro assay, we found more cell adhesion to FN-substrata in PIP than in ESC. Cell locomotion rates on FN-substrata were 1.70 +/- 0.85 microns/min for PIP but only 0.46 +/- 0.56 microns/min for ESC. We also found that the inner surface of the blastocoel roof from ESC can not promote cell adhesion and locomotion when Stage 11 fragments are used for conditioning but that Stage 14 fragments can deposit a FN-fibril-rich extracellular matrix which supports PIP mesodermal cell migration at a rate of 1.26 +/- 0.38 microns/min.     

Migration and Gene Dispersal in Rana pipiens

Although the dominant burnsi gene is widely distributed in Minnesotapopulations of the leopard frog (Rana pipiens) at uniformlylow frequencies, estimates of the effective size of the breedingpopulations suggest that a wider range of gene frequencies mightbe expected due to random genetic drift. Observations of thespring, summer, and fall migrations, however, indicate a levelof migratory activity sufficient to prevent local divergencein gene frequencies. Temperature appears to play a major rolein the springtime migratory and breeding behavior of Rana pipiensin Minnesota.     

Morphological observations on cultured lampbrush-stage Rana pipiens oocytes.

Early lampbrush-stage oocytes are characterized by small lampbrush chromosome loops, a small amount of ribonucleoprotein (RNP) matrix on the loops, small nucleoli, few RNP particles in the nucleoplasm, and a smooth germinal vesicle contour. In vitro culture of these oocytes in serum-free culture medium for 24 hr at 18°C promotes a number of morphological changes in the oocytes: The lampbrush loops increase in diameter and acquire extensive RNP matrix, the nucleoli increase in size and complexity, the nucleoplasm accumulates numerous polymorphic RNP particles, and the germinal vesicle envelope acquires a sacculated contour. These characteristics are typical of the in vivo maximum lampbrush stage, and their appearance is due to an apparent in vitro acceleration of the lampbrush phase. Two possible interpretations of these observations are discussed.     

Sexually dimorphic laryngeal morphology in Rana pipiens

The sexually dimorphic vocal characteristics of Rana pipiens release calls suggest that there may be differences in the anatomical components of the larynx. The volumes of the arytenoid cartilage, surrounding muscle masses, vocal cords, supporting bronchial process, and the release-call amplitudes of six males and five females were measured in same-sized animals and sexual differences assessed. No qualitative differences in laryngeal morphology were observed, but all features measured except vocal cords were significantly larger in males. The implications of an increased laryngeal size are discussed in relation to differences previously observed in the vocalizations of this and other species and in relation to prior suggestions regarding the developmental basis of anuran sexual dimorphisms.