Stereological estimates of nuclear volume correlated with histopathological grading and prognosis of bladder tumour

The aim of this retrospective study is to provide morphometric data which make grading of urinary bladder tumours objective and reproducible by stereological estimation of nuclear volume using the principle of estimating of the volume of particles of arbitrary shape. The study includes 92 specimens: 12 from normal bladder mucosa, and 80 from bladder tumours (15 grade I, 45 grade II, 19 grade III and one grade IV according to Bergkvist et al. 1965). After standard fixation, embedding, sectioning and hematoxylin-eosin staining, an unbiased estimate of the mean volume of nuclei sampled with a change proportional to the volume: (Formula: see text) was calculated. Here l0 is the length of the intercept through a test point hitting a nucleus measured in a random direction through the test point. The weighted means of nuclear volume in bladder tumours are spread over a wide range and show a strong correlation with the Bergkvist grade. Moreover, the relationship between the weighted mean volume of nuclei in bladder tumours and the prognosis is very good. Only one of 35 patients with a mean nuclear volume below 300 micron 3 died of bladder cancer whereas 18 of 19 patients with a mean nuclear volume above 500 micron 3 developed invasives tumours or died of their disease. This simple and fast estimate of nuclear volume seems to provide objective data of high prognostic value.     

On the orientation of foreign neurotransmitter receptors in Xenopus oocytes

Xenopus oocytes can be made to incorporate into their membrane foreign neurotransmitter receptors and voltage-activated sodium channels. In their original location the receptors are normally activated by the extracellular action of transmitter substances. Tests were made to see if some of the newly synthesized foreign receptors were inserted in the oocyte membrane with their active site facing inwards. Since intracellular injections of acetylcholine, gamma-aminobutyric acid, serotonin and kainic acid and tetrodotoxin into the oocyte failed to elicit a response, we conclude that very few, or none, of the receptor molecules expressed in the oocyte by the exogenous mRNA are inserted with the wrong orientation in the membrane.     

Further Studies of Dopamine Metabolism and Function in Tetrahymena1

The large amounts of dopamine accumulated by cells of Tetrahymena pyriformis strain NT-1 and secreted into their growth medium were found to depend primarily upon an extracellular, non-enzymatic conversion of tyrosine to L-dihydroxyphenylalanine (L-DOPA); L-DOPA was then rapidly taken into the ceils and transformed into dopamine enzymatically. Efforts to find physiologically significant dopamine binding sites on the cell surface or dopamine-sensitive adenylate cyclase activity were unsuccessful, suggesting that the catecholamine does not function in Tetrahymena as it does in higher animals.     

A Semivolatile Floral Scent Marks the Shift to a Novel Pollination System in Bromeliads

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SEASONAL CHANGES IN FOOD INTAKE OF HARP SEALS (PHOCA GROENLANDICA) AT 69°N

Food intake (PI), body mass ( BM ), and compartmental growth were recorded for 12 mo in four captive 2–4-yr-old male harp seals ( Phoca groenlandica ), exposed to an artificial light regime that closely resembled natural day length at 69°. In early May before molting, both FZ and BM decreased in all four animals. Total body fat ( TBF ) declined from 51% of BM in March (n = 4) to 30% in August (n = 2), while total body water ( TBW ) concomitantly increased from 37% to 51% and total body protein ( TBP ) from 11% to 17%. In July FI started to increase, while BM started to increase in August. TBF increased while TBW and TBP decreased from August, all three parameters reaching a stable level in October at 47%, 39%, and 12%, respectively. Thereafter, body composition was maintained rather constant until May. Between October and March/April FI fluctuated for all animals, while BM showed a fairly steady increase. Average daily amount of capelin consumed was 2.67 kg·d⁻¹, equivalent to 25,600 kJ·d⁻¹, or 343 kJ·kg⁻¹·d⁻¹.