𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stochastic model for mast cell proliferation in culture of murine peritoneal cells

✍ Scribed by Toshimi Kobayashi; Tatsutoshi Nakahata


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
465 KB
Volume
138
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


We recently identified two types of mast cell colonies derived from murine peritoneal cells: type 1 and type 2. Type 1 mast cell colonies consisted of berberine sulfate( + )-safranin( + ) connective tissue-type mast cells (CTMC) and were derived from mature CTMC in the heaviest fraction obtained by Percoll density gradient centrifugation. In contrast, type 2 mast cell colonies consisted of alcian blue( + )-berberine sulfate(-)-safranin(-) mucosal mast cells (MMC) and were derived from immature progenitors in low density fractions. We replated a total of 60 type 1 and 60 type 2 mast cell colonies and examined their capability for producing secondary colonies. Although all of the primary colonies yielded secondary colonies, the replating efficiencies of individual colonies varied over a wide range.

Cumulative distributions of secondary colonies from both type 1 and type 2 primary colonies could be fitted well by gamma distributions obtained by computer simulation. These findings are in agreement with the stochastic model for CTMC-and MMC proliferation. Cytological analyses of secondary colonies from primary type 1 colonies revealed heterogeneous distributions of alcian blue( + 1safranin(-)-berberine sulfate(-) mast cells, suggesting that transdifferentiation from mature CTMC to safranin(-)-berberine sulfate(-) mast cells is also governed by stochastic mechanisms.


πŸ“œ SIMILAR VOLUMES


A stochastic model for mast cell prolife
✍ Pamela N. Pharr; Jerry Nedelman; Heather P. Downs; Makio Ogawa; Alan J. Gross πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 English βš– 639 KB

A birth-death model was developed for the proliferation of mast cells. According to the model, each secondary mast cell colony starts with one proliferative cell. At each generation each cell chooses among three possibilities: 1 ) division into two proliferative cells; 2) division into two non-proli

Proliferation and differentiation in cul
✍ Toshio Suda; Junko Suda; Samuel S. Spicer; Makio Ogawa πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 English βš– 608 KB

Mice of genotype W/Wv have less than 1% of normal mast cells in the skin, stomach, and cecum. In order to further clarify the mechanism of this deficiency, we studied committed mast cell progenitors and multipotent progenitors, which are capable of mast cell differentiation in clonal culture. The re

Mast cells are required for optimal auto
✍ Gregory D. Gregory; Michaela Robbie-Ryan; Virginia H. Secor; Joseph J. Sabatino πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 324 KB πŸ‘ 1 views

## Abstract Once considered to be of sole importance in allergy and parasitic infections, the role of mast cells in other pathologic and protective immune responses is becoming increasingly evident. We previously demonstrated that mast cells contribute to the severity of EAE, the rodent model of mu

Experimental model for observation of mi
✍ MaΕ‚gorzata Lewandowska-SzumieΕ‚; Krzysztof Sikorski; Andrzej Szummer; Janusz Kome πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 252 KB

## Abstract It is known that the micromotion between implant and bone inhibits direct bone growth either on or into implant surfaces __in vivo__. Nevertheless, biocompatibility tests __in vitro__ of biomaterials for bone/implant interfaces are mainly performed under static conditions. This work des