Paracrine and
autocrine signals induce and maintain mesenchymal and stem cell states in the breast.
Not exact matches
Consequently, we conclude that the classical endotheliocentric view of Tie2
signalling with Ang1 acting in a paracrine manner and Ang2 through an
autocrine loop needs to be revised in favour of a bi-directional reciprocal model in which the EC
signalling is complemented reciprocally by an
autocrine Ang1 / Tie2 loop in pericytes and paracrine acting Ang2 (Fig. 7).
These factors, along with stem cell
autocrine factors such as nodal and GDF - 3, might maintain a high local ratio of SMAD2 / 3 to SMAD1
signaling to drive stem cell maintenance.
Peerani et al. [31] suggested that there is a minimal colony size effect the maintenance of human ES cell pluripotency, and provided evidence that
autocrine regulators of BMP and nodal
signaling are key components of this regulatory pathway.