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Notch Signaling Pathway03:14

Notch Signaling Pathway

The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not until 1985...
Notch Signaling Pathway03:14

Notch Signaling Pathway

The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not until 1985...
Catenins01:23

Catenins

Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the adherens...
Non-Canonical Wnt Signaling Pathways01:41

Non-Canonical Wnt Signaling Pathways

Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...
Renewal of Skin Epidermal Stem Cells01:12

Renewal of Skin Epidermal Stem Cells

The skin is divided into epidermis, dermis, and hypodermis, the skin's outermost, middle, and inner layers. The human epidermal layer regularly undergoes renewal, where old, dead cells are replaced by new cells. Epidermal stem cells or EpiSCs divide and differentiate to restore the lost cells. For the renewal process, some EpiSCs continuously self-renew. In contrast, few others differentiate into transit-amplifying cells, which later form prickle or spinous cells, followed by granular cells,...
Role of Skin in Vitamin D Synthesis01:23

Role of Skin in Vitamin D Synthesis

The skin plays a crucial role in the synthesis of vitamin D, a vital nutrient for various physiological processes in the body. Vitamin D is unique because it can be synthesized in the skin through a series of chemical reactions triggered by exposure to ultraviolet B (UVB) radiation from sunlight.
The solar UV B rays (290-315 nm) are absorbed by the skin, and 7-dehydrocholesterol (provitamin D3) photolyzes it to previtamin D3, which undergoes a rapid transformation to vitamin D3(cholecalciferol).

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Related Experiment Video

Updated: Jun 2, 2026

In Vitro Investigation of the Effects of the Hyaluronan-Rich Extracellular Matrix on Neural Crest Cell Migration
11:16

In Vitro Investigation of the Effects of the Hyaluronan-Rich Extracellular Matrix on Neural Crest Cell Migration

Published on: February 10, 2023

CCN2 is not required for skin development.

Shangxi Liu1, Andrew Leask

  • 1Division of Oral Biology and Department of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, University of Western Ontario, Dental Sciences Bldg., London, ON, Canada, N6A 5C1.

Journal of Cell Communication and Signaling
|May 3, 2011
PubMed
Summary
This summary is machine-generated.

Connective tissue growth factor (CTGF/CCN2) is not essential for embryonic skin development, despite its known role in bone and cartilage formation. Studies show CCN2 is unnecessary for skin thickness or vascular and smooth muscle cell development.

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Culturing and Manipulation of O9-1 Neural Crest Cells

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Isolation and Culture of Primary Mouse Keratinocytes from Neonatal and Adult Mouse Skin
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Isolation and Culture of Primary Mouse Keratinocytes from Neonatal and Adult Mouse Skin

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Last Updated: Jun 2, 2026

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11:16

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Isolation and Culture of Primary Mouse Keratinocytes from Neonatal and Adult Mouse Skin
10:51

Isolation and Culture of Primary Mouse Keratinocytes from Neonatal and Adult Mouse Skin

Published on: July 14, 2017

Area of Science:

  • Developmental biology
  • Extracellular matrix biology
  • Connective tissue research

Background:

  • Connective tissue growth factor (CTGF/CCN2) is a matricellular protein crucial for embryonic development, particularly in bone and cartilage.
  • Previous research indicated embryonic lethality in mice lacking CTGF/CCN2 due to skeletal defects.
  • The specific role of CTGF/CCN2 in embryonic skin development remained undetermined.

Purpose of the Study:

  • To investigate the necessity of CTGF/CCN2 for proper skin development during embryogenesis.
  • To determine if CTGF/CCN2 plays a role in the formation of skin structures like thickness, vasculature, and smooth muscle.

Main Methods:

  • Generation of whole-body CTGF/CCN2 knockout mice using a cre/lox system with constitutive cre recombinase expression.
  • Assessment of skin development through measurements of skin thickness.
  • Histological analysis using trichrome staining.
  • Immunostaining with anti-CD31 and anti-α-SMA antibodies to evaluate endothelial cells, smooth muscle cells, and pericytes.

Main Results:

  • Mice lacking CTGF/CCN2 did not exhibit developmental defects in skin thickness.
  • Trichrome staining revealed no significant differences in skin structure between knockout and wild-type mice.
  • Immunostaining confirmed normal development of endothelial cells (CD31+) and smooth muscle cells/pericytes (α-SMA+) in the skin of knockout mice.

Conclusions:

  • CTGF/CCN2 is not required for the embryonic development of mouse skin.
  • Despite its critical role in other embryonic tissues and postnatal fibrogenesis, CTGF/CCN2 is dispensable for the formation of skin structures during embryogenesis.