Comparison of stem-cell recovery in autoimmune and normal strains

The capacity of NZB stem cells to proliferate in vivo was evaluated in two systems which required repopulation of peripheral organs. In both types of depletion systems, stem-cell repopulation after cyclophosphamide treatment or adoptive transfer repopulation in lethally irradiated hosts, it was found that NZB stem cells were hyperproliferating. The increase in proliferating cells was most pronounced in the spleens of NZB mice treated with high-dose cyclophosphamide and in lethally irradiated F₁ mice reconstituted with NZB T-cell-depleted bone marrow. Thus, upon a stimulus to repopulate, NZB marrow stem cells will hyperproliferate in peripheral organs resulting in an increase in cell number. The abnormality in the marrow cells can be observed in young NZB mice when their marrow cells are in an environment which requires recovery and division.     

Structural studies of an Inv (1, −2) kappa light chain

A Bence Jones protein with phenotype Inv (1, –2) was isolated from the urine of a patient with multiple myeloma. Inv typing of the patient's relatives established the presence of anInv ¹ allele in the kindred, and that the patient's genotype wasInv ¹/Inv ³. Hence, the absence of Inv (2) in the Bence Jones protein was shown to be genetic and not an artifact caused by the disease. The tryptic peptide-containing residues 191 through 194 were isolated and shown to be composed of Leu, Tyr, Ala, Cys, with Leu at the amino end. Hence, the residue at 191 is the same as that present in Inv (1, 2) Bence Jones proteins. More detailed study of the tryptic peptides established that residue 153 is Val rather than Ala as in all other K chains thus far studied. The primary sequence: Ala¹⁵³, Leu¹⁹¹ determines Inv (1, 2); Ala¹⁵³, Val¹⁹¹ determines Inv (3); and Val¹⁵³, Leu¹⁹¹ determines Inv (1). The Val¹⁵³, Val¹⁹¹ sequence has not been observed. It may correspond to Inv (–). These data are strikingly similar to the data for the Kern and Oz isotypes (changes at 154 and 191, respectively) in the chain. As in the case of theK chain, only three of the four possible combinations have been observed. The implications of this parallelism and of crystallographic findings on chains, reported by others, are discussed.     

COMPARISON OF DAYLENGTH AND TEMPERATURE RESPONSES IN NICOTIANA AND ITS TAXONOMIC SECTIONS

Steinberg , Robert A. (U.S.D.A., Beltsville, Md.) Comparison of daylength and temperature responses in Nicotiana and its taxonomic sections. Amer. Jour. Bot. 46(4): 261–268. Illus. 1959.—Fifty-seven of the sixty species of Nicotiana were grown in the greenhouse under long- and short-day regimes. Supplemental tungsten light of about 30 ft.-c. (bench) was used to extend natural illumination to 16 hr. daily. Short-day controls received natural illumination for 9.5–12 hr. daily from about September to March. Two temperature levels were also employed—one with temperature held uniformly at about 25°C. and the other with a day temperature of about 20°C. and a night temperature of about 10°C. Daylength behavior of the species ranged from long-day to day-neutral to short-day. All species were brought into flower and all, except N. acaulis and N. ameghinoi, formed viable seed in at least 1 of the 4 environments. A modified classification of photoperiodic flowering responses based on rapidity and not ability to flower was adopted to permit quantitative comparison of species responses to both daylength and temperature. Very few species flowered equally rapidly (day-neutral) in both the 10- and 16-hr. day-lengths. Temperature level caused modifications in response from long-day to day-neutral and vice versa, and from short-day to day-neutral and vice versa. Data for N. glauca and some other species would indicate that a greater spread between temperature levels could possibly lead to opposite classifications at upper and lower temperatures. Excellent agreement was found between daylength responses of the species and the 14 taxonomic sections of Goodspeed for the genus Nicotiana. Only 2 of the sections (Paniculatae and Undulatae) were heterogeneous in that both included short- and long-day species in the same section. The native habitat of all short-day species was South America. Certain of the species gave a compensatory response to variations in light duration and low temperature similar to that given by sugarbeets and other biennials. This phenomenon may therefore be of general occurrence. Use of a quantitative expression for photoperiodic flowering responses is proposed to avoid ambiguity. It is the quotient of days from sowing to first blossom on short-days divided by that on long-days. The value 0.6₂₀°C. (9–12) would read short-day at 20°C. with 9–12 hr. daylengths. Close agreement was found in daylength flowering ratios in successive tests in the greenhouse. The ratios alter under cold treatment with species susceptible to low-temperature stimulation or inhibition of blossoming.     

Synthesis of ribonucleic acid in normal bone in vitro

1. The incorporation of [2-(14)C]uridine into nucleic acids of bone cells was studied in rat and pig trabecular-bone fragments surviving in vitro. 2. The rapid uptake of uridine into trichloroacetic acid-soluble material, and its subsequent incorporation into a crude nucleic acid fraction of bone or purified RNA extracted from isolated bone cells, was proportional to uridine concentration in the incubation medium over a range 0.5-20.0mum. 3. During continued exposure to radioactive uridine, bulk RNA became labelled in a curvilinear fashion. Radioactivity rapidly entered nuclear RNA, which approached its maximum specific activity by 2hr. of incubation; cytoplasmic RNA, and particularly microsomal RNA, was more slowly labelled. The kinetics of labelling and rapid decline of the nuclear/microsomal specific activity ratio were consistent with a precursor-product relationship. 4. Bulk RNA preparations were resolved by zonal centrifugation in sucrose density gradients into components with approximate sedimentation coefficients 28s, 18s and 4s. 5. Rapidly labelled RNA, predominantly nuclear in location, demonstrated a polydisperse sedimentation pattern that did not conform to the major types of stable cellular RNA. Material of highest specific activity, sedimenting in the 4-18s region and insoluble in 10% (w/v) sodium chloride, rapidly achieved its maximum activity during continued exposure to radioactive precursor and decayed equally rapidly during ;chase' incubation, exhibiting an average half-life of 4.3hr. 6. Ribosomal 28s and 18s RNA were of lower specific activity, which increased linearly for at least 6hr. in the continued presence of radioactive uridine. There was persistent but variable incorporation into ribosomal RNA during ;chase' incubation despite rapid decline in total radioactivity of the acid-soluble pool containing RNA precursors.