bioRxiv Science⌕ Search

Biology subjects

Iyengar, V.

Publications and source records attributed to Iyengar, V..

2 recordsLinked to original sources

Age-specific and Sex-specific Nectar and Pollen Use by a Butterfly Pollinator

Age-specific patterns of nectar and pollen use by insect pollinators may reflect behavioral or physiological changes over the insects lifespan, and may also influence flower visitation rate. Studying Heliconius charithonia (Lepidoptera: Nymphalidae) and Psiguria umbrosa (Cucurbitaceae), we showed that honey-water (as a nectar substitute) intake increases over the first ten to twelve days of females life, while decreasing over the same age period for males, when individuals were fed ad libitum. Intake then remains stable at least through 28 days of age. Mean intake is higher for females than for males, and is not significantly affected by body size. Intake patterns for honey-water and pollen did not change with age in a similar manner. Pollen feeding increased significantly with age for both sexes, with females showing a two week delay in the increase when studied in a free-flying greenhouse population with competition for pollen. Under both ad libitum and pollen competition conditions, females collected more pollen than did males. Body size did not significantly affect the amount of pollen collected for either sex. Within each sex, butterflies with ad libitum pollen collected more pollen than those in a free-flying greenhouse population with more restricted pollen availability. These results suggest that two resources obtained from the same source, pollen and nectar, are not treated identically by the insect pollinator, and that the demography of the insect population may affect flower visitation rates in some cases. Further, foraging patterns for pollen and nectar are likely driven by physiological demand for different resource types.

ecology↗

Identification Of A Native Novel Oncolytic Immunoglobulin On Exfoliated Colon Epithelial Cells: A Bispecific Heterodimeric Chimera Of IgA/IgG

Understanding the nature of cell surface markers on exfoliated colonic cells is a crucial step in establishing criteria for a normally functioning mucosa. We have found that colonic cells isolated from stool samples (SCSR-010 Fecal Cell Isolation Kit, NonInvasive Technologies, Elkridge, MD), preserved at room temperature for up to one week, with viability of >85% and low levels of apoptosis (8% - 10%) exhibit two distinct cell size subpopulations, in the 2.5M- 5.0 M and 5.0M-8.0M range. In addition to IgA, about 60% of the cells expressed a novel heterodimeric IgA/IgG immunoglobulin that conferred a broad-spectrum cell mediated cytotoxicity against tumor cells. In a cohort of 58 subjects the exclusive absence of this immunoglobulin in two African-Americans was suggestive of a germline deletion. Serial cultures in stem cell medium retained the expression of this heterodimer. Since a majority of the cystic cells expressed the stem cell markers Lgr5 and Musashi-1 we termed these cells as gastrointestinal progenitor stem cells (GIP-C**). CXCR-4, the cytokine co-receptor for HIV was markedly expressed. These cells also expressed CD20, IgA, IgG, CD45, and COX-2. We assume that they originated from mature columnar epithelium by dedifferentiation. Our observations indicate that we have a robust noninvasive method to study mucosal pathophysiology and a direct method to create a database for applications in regenerative medicine.

cell biology↗