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Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein.

Aortic carboxypeptidase-like protein (ACLP) is a member of a diverse group of proteins that contain a domain with similarity to that of the Dictyostelium discoideum protein discoidin I. The discoidin domain has been identified in mammalian milk fat globule membrane proteins, blood coagulation factors, and receptor tyrosine kinases, where it may facilitate cell aggregation, adhesion, or cell-cell recognition. Here we show that ACLP is a secreted protein that associates with the extracellular matrix (ECM). During mouse embryogenesis, ACLP is abundantly expressed in the ECM of collagen-rich tissues, including the vasculature, dermis, and the developing skeleton. We deleted the ACLP gene in mice by homologous recombination. The majority of ACLP(-/-) mice die perinatally due to gastroschisis, a severe disruption of the anterior abdominal wall and herniation of the abdominal organs. ACLP(-/-) mice that survived to adulthood developed nonhealing skin wounds. Following injury by a dermal punch biopsy, ACLP(-/-) mice exhibited deficient wound healing compared with controls. In addition, dermal fibroblasts isolated from ACLP(-/-) 18.5-day-postconception embryos exhibited a reduced proliferative capacity compared with wild-type cells. These results indicate that ACLP is an ECM protein that is essential for embryonic development and dermal wound healing processes.

Pubmed ID: 11438679

Authors

  • Layne MD
  • Yet SF
  • Maemura K
  • Hsieh CM
  • Bernfield M
  • Perrella MA
  • Lee ME

Journal

Molecular and cellular biology

Publication Data

August 4, 2001

Associated Grants

  • Agency: NHLBI NIH HHS, Id: HL10113
  • Agency: NHLBI NIH HHS, Id: HL57977

Mesh Terms

  • Abdominal Muscles
  • Animals
  • Bone Development
  • Carboxypeptidases
  • Cell Adhesion
  • Cell Aggregation
  • Cell Division
  • Cells, Cultured
  • Cloning, Molecular
  • Collagen
  • Extracellular Matrix
  • Immunohistochemistry
  • Mice
  • Microscopy, Fluorescence
  • Models, Genetic
  • Muscle, Smooth
  • Mutagenesis, Site-Directed
  • Phenotype
  • Protein Structure, Tertiary
  • Proteins
  • Recombination, Genetic
  • Repressor Proteins
  • Skin
  • Subcellular Fractions
  • Time Factors
  • Wound Healing