Differential regulation of the chick dorsal thoracic dermal progenitors from the medial dermomyotome.

Development

Equipe Biologie de la Différenciation Epithéliale, UMR CNRS 5538, LEDAC, Institut Albert Bonniot, Université Joseph Fourier, Grenoble, France.

Published: October 2002

The chick dorsal feather-forming dermis originates from the dorsomedial somite and its formation depends primarily on Wnt1 from the dorsal neural tube. We investigate further the origin and specification of dermal progenitors from the medial dermomyotome. This comprises two distinct domains: the dorsomedial lip and a more central region (or intervening zone) that derives from it. We confirm that Wnt1 induces Wnt11 expression in the dorsomedial lip as previously shown, and show using DiI injections that some of these cells, which continue to express Wnt11 migrate under the ectoderm, towards the midline, to form most of the dorsal dermis. Transplantation of left somites to the right side to reverse the mediolateral axis confirms this finding and moreover suggests the presence of an attractive or permissive environment produced by the midline tissues or/and a repellent or inadequate environment by the lateral tissues. By contrast, the dorsolateral dermal cells just delaminate from the surface of the intervening space, which expresses En1. Excision of the axial organs or the ectoderm, and grafting of Wnt1-secreting cells, shows that, although the two populations of dermal progenitors both requires Wnt1 for their survival, the signalling required for their specification differs. Indeed Wnt11 expression relies on dorsal neural tube-derived Wnt1, while En1 expression depends on the presence of the ectoderm. The dorsal feather-forming dermal progenitors thus appear to be differentially regulated by dorsal signals from the neural tube and the ectoderm, and derive directly and indirectly from the dorsomedial lip. As these two dermomyotomal populations are well known to also give rise to epaxial muscles, an isolated domain of the dermomyotome that contains only dermal precursors does not exist and none of the dermomyotomal domains can be considered uniquely as a dermatome.

Download full-text PDF

Source
http://dx.doi.org/10.1242/dev.129.20.4763DOI Listing

Publication Analysis

Top Keywords

dermal progenitors
16
dorsomedial lip
12
chick dorsal
8
progenitors medial
8
medial dermomyotome
8
dorsal feather-forming
8
dorsal neural
8
neural tube
8
wnt11 expression
8
dorsal
7

Similar Publications

Fibroblasts display complex functions associated with distinct gene expression profiles that influence matrix production and cell communications and the autonomy of tissue development and repair. Thrombospondin-2 (TSP-2), produced by fibroblasts, is a potent angiogenesis inhibitor and negatively associated with tissue repair. Single-cell (sc) sequencing analysis on WT and TSP2KO skin fibroblasts demonstrate distinct cell heterogeneity.

View Article and Find Full Text PDF

Adipose tissue, or fat compartments, has long been considered a storage depot and an energy source. However, a large part of new research, starting with the discovery of adipose-derived stem cells, has redirected this thinking toward the tremendous regenerative capacity that adipose tissue possesses when it is healthy. This has resulted in multiple technologies being explored with fat as a basis or with fat as a target aiming at the stimulation of new small hyperplastic adipose cells exuding adipokines and encouraging the proliferation of a whole host of progenitor cells that can have positive effects on many organ systems.

View Article and Find Full Text PDF

Engineered biomimetic nanovesicles-laden multifunctional hydrogel enhances targeted therapy of diabetic wound.

Mater Today Bio

December 2024

Department of Hand Surgery, Union Hospital, Tongji Medical College, Huazhong, University of Science and Technology, Wuhan, 430022, China.

Article Synopsis
  • Angiogenesis is crucial for healing diabetic wounds, and endothelial progenitor cell-derived extracellular vesicles (EPC-EVs) can enhance this process, but their use is limited by low yield and targeting issues.
  • The study developed biomimetic nanovesicles (EPC-NV) from EPCs and modified them with cRGD peptides (mEPC-NV) for better targeting of endothelial cells.
  • A dual hydrogel network was created that combined an acellular dermal matrix with light-cured gelatin to sustainably release mEPC-NV while providing antioxidant and antibacterial properties, making it a promising approach for diabetic wound treatment.
View Article and Find Full Text PDF
Article Synopsis
  • An 11-year-old girl developed severe Grade IV skin graft-versus-host disease resembling toxic epidermal necrolysis after receiving hematopoietic progenitor cell transplantation from a fully compatible unrelated donor.
  • On the 35th day post-transplant, she exhibited rash-like lesions, and a skin biopsy confirmed a diagnosis of TEN-like acute cutaneous GVHD, highlighting serious skin damage and inflammation.
  • After adjusting her immunosuppressant medications, the patient achieved an 80% reduction in symptoms, indicating a positive response to treatment.
View Article and Find Full Text PDF
Article Synopsis
  • Astragaloside IV (ASIV) enhances the growth of endothelial progenitor cells (EPCs), which are crucial for wound healing, while a new composite delivery system (PF-PEG@ASIV-EXO) utilizes exosomes and hydrogels to target these cells effectively.
  • The study evaluated the biocompatibility of the PF-PEG@ASIV-EXO system and its effects on EPC function, including cell viability, blood vessel formation (angiogenesis), and cellular health in high-glucose environments resembling diabetes.
  • Results from diabetic rat wounds showed that PF-PEG@ASIV-EXO not only increased the healing process but also elevated important markers for blood vessels and reduced harmful cell death,
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!