Distribution and identity of the earliest proliferating progeny of colony-forming cells in regenerating murine spleen and bone marrow
✍ Scribed by Wolf, Norman ;Rosse, Cornelius
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1982
- Tongue
- English
- Weight
- 889 KB
- Volume
- 163
- Category
- Article
- ISSN
- 0002-9106
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A study was made of the sites of development and the types of cells found in very early hemopietic colomes in the mouse spleen. Two, 3, and 4 days after transplantation, the proliferating descendants of transplanted bone‐marrow cells were identified on radioautographs of spleen sections and on spleen and bone‐marrow smears of supralethally irradiated recipient mice which were injected with ^3^H‐TdR at 12, 6, and 0.5 hours before sacrifice. Surprisingly the spleens of nontransplanted, irradiated mice contained proliferating medium and large lymphocytes in the white pulp which increased in numbers during the observation period. The early descendants of transplanted cells that lodged in the spleen could be clearly distinguished from the labeled indigenous cells because they formed discrete nodules or colonies beneath the splenic capsule or in the vicinity of venules and trabeculae of the red pulp. These cells were identifiable on day 2 as transitional cells or unknown hemopoietic blasts and on day 4 included early erythroid cells and small lymphocytes. There was evidence for the traffic of ^3^H‐TdR‐labeled cells through the splenic sinusoids.
📜 SIMILAR VOLUMES
The two crystalline forms of CaCO 3 , aragonite (from natural coral) and calcite (from natural limestone), have been used with success as bone graft substitutes. However, natural coral transformed into calcite by heating has never been tested. The objective of this work was to study the proliferatio
UDP-GlcNAc:Galb1 r 3GalNAc-R b1 r 6N-acetylglucosaminyltransferase (Core2 N-acetyl-glucosaminyltransferase, C2GnT; EC 2.4.1.102) forms b1 r 6Nacetyl-glucosaminyl linkages in O-glycoproteins and creates branches for the addition of N-acetyl-lactosamine antennae. Changes in C2GnT activity have been as