The scanning behavior of juncos: A game-theoretical approach

Flocking birds frequently look up or “scan” while they are feeding on the ground. High scanning rates increase the probability that the birds in a flock will see an approaching predator in time to avoid predation; however, high scanning rates also decrease the feeding rates of the scanning individuals. Since the scanning rate that maximizes the survival probability of one individual depends on how frequently other birds in the same flock are scanning, the optimal scanning behavior must be modeled as a game. We develop a realistic model of scanning behavior and use it to find two game theoretical solutions—the “co-operative” or Pareto optimum and the “selfish” or Nash optimum. The observed scanning rates do not differ significantly from the co-operative optimal scanning rate. We argue that in a game where players meet again and again such apparent co-operation may be an evolutionarily stable strategy.     

Murine fetal colon in vitro: assays for growth factors

The growth of murine fetal colon was examined in two tissue-culture systems: an organ-culture assay and a modified Hamburger assay for the production of cell colonies in a semi-solid medium. The organ-culture system was found to support the normal development of the intact colon for several weeks, but epithelium separated from mesenchyme produced terminal squamous differentiation within 1 week. Gastrin analogues permitted continued growth of the epithelium, but produced a maturation arrest which was reversible by the removal of the hormone and after prolonged culture. Epidermal growth factor (EGF) produced some mesenchymal proliferation but, as with the other reagents tested, had no effect on the epithelium in organ culture. Analogues of gastrin produced enhanced colony formation in cells from fetal colon and neonatal colon obtained up to 2 weeks post-partum, but had no effect on adult colon. No enhanced colony formation was seen with EGF, oestrogen, dexamethasone, indomethacin, progesterone, prolactin and testosterone. Mouse fetal colon in organ culture can be a useful model for screening possible trophic factors for the colon in a qualitative way, while the colony-assay system can be used to provide quantitative results.     

Height at diagnosis of diabetes in children: a study in identical twins.

The height at diagnosis of 16 insulin dependent diabetics aged under 19 was compared with that of their unaffected identical cotwins measured at the same time. In eight pairs the diabetic was shorter, and in the remainder the cotwins were the same height. In those diabetics who were shorter than their cotwins at diagnosis the average period of growth delay before diagnosis was at least 35 weeks; by contrast, the mean duration of symptoms was only six weeks. No cause for the growth delay other than the diabetes was known in any of the twins. These findings show that the onset of insulin dependent diabetes may be a slow process, with growth delay occurring several months before symptoms appear.     

Detection of T-precursor cells in human bone marrow and foetal liver.

Human lymphoid cells that have been incubated with conditioned medium from confluent monolayers of human thymic epithelium (HTCM) show an increase in cells forming rosettes with sheep erythrocytes at 4 degrees C (E-rosettes). Those cells demonstrating this in vitro conversion have been interpreted to be T-cell precursors. Separation of human bone marrow cells on discontinuous bovine serum albumin (BSA) gradients, and on a single-step 23% BSA gradient showed enrichment of these T-precursor cells, not only in bone marrow, but also in human foetal liver cells. Bone marrow precursor cells from a patient with Wiskott-Aldrich syndrome (T-cell deficiency) showed a normal in vitro response to HTCM, but no response was seen in cells from a patient with severe combined immunodeficiency disease.     

Plasminogen activator inhibitor (type-1) in rat adrenal medulla

Plasminogen activator inhibitor type-1 (PAI-1) was identified in extracts of rat adrenal medulla, and its immunohistochemical localization was studied together with that of tissue-type plasminogen activator (t-PA). By staining of adjacent sections and by double-staining of the same section we demonstrate that the same cells of the adrenal medulla contain both PAI-1 and t-PA immunoreactivity in the cytoplasm. In addition a few ganglion cells of the adrenal medulla were found to contain PAI-1 but not t-PA. Neither of the components were found in the adrenal cortex. Analysis of extracts from isolated adrenal medulla using reverse zymography showed the presence of a plasminogen activator inhibitor with Mr approximately 46,000. The inhibitory activity disappeared when the extract was passed through a column with sepharose-coupled anti-PAI-1 IgG, while the run-through from a similar column coupled with preimmune IgG still contained the inhibitor. The present findings suggest that PAI-1 could play a role in the regulation of t-PA activity in the rat adrenal gland medullary cells.     

Confirmation of a susceptibility locus on chromosome 13 in Australian breast cancer families

Two major genes determining predisposition to breast cancer, termed BRCA1 and BRCA2, have been mapped to the long arms of chromosomes 17 and 13, respectively. Each locus is believed to account for approximately 40% of cases of familial breast cancer. We used linkage and haplotype analysis with simple tandem repeat polymorphisms at chromosomal bands 17q21 and 13q12 to determine the contribution of the BRCA1 and BRCA2 genes to predisposition to breast cancer in four Australian breast cancer kindreds, one of which had two male cousins with breast cancer. Surprisingly all families segregated a haplotype of markers on 13q and showed positive lod scores supporting linkage to BRCA2. In addition, haplotype analysis identified an informative recombination between D13S260 and D13S171 in one affected individual, which refines the localisation of BRCA2 to between D13S260 and D13S267; a distance of 2–3 cM. Tumours of the stomach and cervix, as well as melanoma and leukaemia/lymphoma also occur in these pedigrees but the numbers are too low to determine whether they may be significantly associated with BRCA2 carrier status. Our results confirm the existence of BRCA2 on the long arm of chromosome 13 and support previous findings that this locus is likely to confer risk in families with affected males. Furthermore, our observations suggest that the BRCA2 gene may also contribute to the development of other neoplasms. Received: 26 September 1995 / Revised: 15 January 1996