S5.6 Sponge cell aggregation — The functional implication of carbohydrate epitopes in cellular interactions

1993 ◽  
Vol 10 (4) ◽  
pp. 251-252
Author(s):  
D. Spillmann ◽  
K. H⫗aard ◽  
J. Thomas-Oates ◽  
J. F. G. Vliegenthart ◽  
M. M. Burger ◽  
...  
Development ◽  
1966 ◽  
Vol 16 (3) ◽  
pp. 519-530
Author(s):  
Michael Edidin

Treatment with chelating agents binding divalent cations has been found to effect the dissociation of a variety of tissues of both embryo and adult animals (reviewed in Steinberg, 1958). In the course of dissociation it appears that materials are released from cell surfaces which play a part in their specific adhesion, and which may be shown experimentally to promote selectively the re-aggregation of dissociated cells (Humphreys, 1963; Moscona, 1963). The extracted materials appear to be glycoprotein complexes (Humphreys, 1965), made up of fairly small subunits, estimated to be of 13000–20000 molecular weight (Margoliash et al. 1965). Units of about the same size appear to be the antigenic sites involved in the blocking of sponge cell aggregation by rabbit anti-sponge serum, specific for a given sponge species (MacLennan, 1963). I shall here present evidence that materials of similar molecular weight bearing immunological specificities of the H-2 alloantigen system are released from the tissues of certain mouse embryos during the course of their dissociation by the chelating agent Versene (ethylenediaminetetraacetic acid).


1971 ◽  
Vol 230 (12) ◽  
pp. 126-128 ◽  
Author(s):  
H. A. JOHN ◽  
M. S. CAMPO ◽  
A. M. MACKENZIE ◽  
R. B. KEMP

2014 ◽  
Vol 134 (1) ◽  
pp. 1-18 ◽  
Author(s):  
Dafne Eerkes-Medrano ◽  
Colette J. Feehan ◽  
Sally P. Leys

Development ◽  
1991 ◽  
Vol 113 (1) ◽  
pp. 217-225 ◽  
Author(s):  
S. Cascio ◽  
K.S. Zaret

Previous studies with embryonic tissue explants showed that cellular interactions with mesenchyme are required for endodermal cells to differentiate into hepatocytes. However, these studies assayed hepatocyte characteristics that were evident after days of culture, leaving open the question of whether the primary inductive interactions initiated hepatocyte differentiation, or whether subsequent steps, such as may occur during cell aggregation to form the liver, were necessary. Using the technique of in situ hybridization, we find that serum albumin mRNA, a liver-specific gene product, is first detected in hepatic precursor cells of the endoderm as early as 9.5 days of mouse embryo development, a full day prior to cell aggregation and liver formation. The endodermal cells express albumin mRNA upon migration into strands of connective tissue matrix within mesenchyme. Thus, the onset of differentiation of the endoderm is coincident with its interaction with mesenchyme. Early albumin transcripts are initiated at the same site of the albumin promoter as in adult hepatocytes, suggesting that at least a subset of the transcription factors that control albumin transcription in the adult may be involved in executing the early steps of hepatic determination. We also observe a sharp increase in albumin mRNA levels shortly after the definitive formation of the liver, apparently reflecting cell interactions that enhance hepatocyte differentiation. Hepatocyte differentiation is therefore similar in several respects to pancreatic exocrine cell development, and may represent a general pattern for gut-derived tissues. For both cell types, early interactions with mesenchyme are coincident with the initial expression of differentiated gene products at a low level in proliferating endoderm, and the initial pattern of expression is amplified upon organ formation.


1987 ◽  
Vol 170 (2) ◽  
pp. 381-401 ◽  
Author(s):  
Deirdre R. Coombe ◽  
Karen B. Jakobsen ◽  
Christopher R. Parish

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