Literature DB >> 15749083

Aortic carboxypeptidase-like protein is expressed in collagen-rich tissues during mouse embryonic development.

Bonna Ith1, Jiao Wei, Shaw-Fang Yet, Mark A Perrella, Matthew D Layne.   

Abstract

Aortic carboxypeptidase-like protein (ACLP) was originally identified in vascular smooth muscle cells and contains discoidin and catalytically inactive metallocarboxypeptidase domains. ACLP is a secreted protein that associates with the extracellular matrix and is essential for abdominal wall development and contributes to dermal wound healing. Because of these developmental and adult phenotypes, we examined the expression of ACLP by immunohistochemistry throughout mouse embryonic development. ACLP was not detected in 7.5 days post-coitum (dpc) embryos, however at 9.5 dpc low levels of expression were detected in the somites and dorsal aorta. Expression was detected in both the yolk sac and embryonic vasculature at 10.5d pc. ACLP expression increased in both large and small blood vessels at 11.5 and 13.5 dpc and intense expression was detected within the vascular smooth muscle layer in 16.5 dpc embryos. At later developmental time points, discrete areas of ACLP expression were detected in the mesenchymal cells in the dermal layer, developing skeletal structures, connective tissue, and in the umbilical ring and vessels. The predominance of ACLP immunoreactivity localized with collagen-rich regions including tendons and basement membranes. Overall, the developmental expression pattern is consistent with a regulatory or structural role in the abdominal wall, vasculature, and dermis.

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Year:  2004        PMID: 15749083     DOI: 10.1016/j.modgep.2004.11.002

Source DB:  PubMed          Journal:  Gene Expr Patterns        ISSN: 1567-133X            Impact factor:   1.224


  14 in total

Review 1.  Discoidin domain receptors: unique receptor tyrosine kinases in collagen-mediated signaling.

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Journal:  J Biol Chem       Date:  2013-01-18       Impact factor: 5.157

2.  Stable methylation at promoters distinguishes epiblast stem cells from embryonic stem cells and the in vivo epiblasts.

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Journal:  Stem Cells Dev       Date:  2014-06-12       Impact factor: 3.272

3.  Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue.

Authors:  Anas M Alazami; Sarah M Al-Qattan; Eissa Faqeih; Amal Alhashem; Muneera Alshammari; Fatema Alzahrani; Mohammed S Al-Dosari; Nisha Patel; Afaf Alsagheir; Bassam Binabbas; Hamad Alzaidan; Abdulmonem Alsiddiky; Nasser Alharbi; Majid Alfadhel; Amal Kentab; Riza M Daza; Martin Kircher; Jay Shendure; Mais Hashem; Saif Alshahrani; Zuhair Rahbeeni; Ola Khalifa; Ranad Shaheen; Fowzan S Alkuraya
Journal:  Hum Genet       Date:  2016-03-29       Impact factor: 4.132

Review 4.  The Ehlers-Danlos syndromes.

Authors:  Fransiska Malfait; Marco Castori; Clair A Francomano; Cecilia Giunta; Tomoki Kosho; Peter H Byers
Journal:  Nat Rev Dis Primers       Date:  2020-07-30       Impact factor: 52.329

5.  Enhancement of pituitary adenoma cell invasion and adhesion is mediated by discoidin domain receptor-1.

Authors:  Daizo Yoshida; Akira Teramoto
Journal:  J Neurooncol       Date:  2006-09-26       Impact factor: 4.130

6.  Aortic carboxypeptidase-like protein is expressed in fibrotic human lung and its absence protects against bleomycin-induced lung fibrosis.

Authors:  Scott L Schissel; Sarah E Dunsmore; Xiaoli Liu; Robert W Shine; Mark A Perrella; Matthew D Layne
Journal:  Am J Pathol       Date:  2009-01-29       Impact factor: 4.307

7.  Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and -independent pathways.

Authors:  Kathleen E Tumelty; Barbara D Smith; Matthew A Nugent; Matthew D Layne
Journal:  J Biol Chem       Date:  2013-12-16       Impact factor: 5.157

8.  Mechanisms of aortic carboxypeptidase-like protein secretion and identification of an intracellularly retained variant associated with Ehlers-Danlos syndrome.

Authors:  Neya Vishwanath; William J Monis; Gwendolyn A Hoffmann; Bhavana Ramachandran; Vincent DiGiacomo; Joyce Y Wong; Michael L Smith; Matthew D Layne
Journal:  J Biol Chem       Date:  2020-06-01       Impact factor: 5.157

9.  Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.

Authors:  Patrick R Blackburn; Zhi Xu; Kathleen E Tumelty; Rose W Zhao; William J Monis; Kimberly G Harris; Jennifer M Gass; Margot A Cousin; Nicole J Boczek; Mario V Mitkov; Mark A Cappel; Clair A Francomano; Joseph E Parisi; Eric W Klee; Eissa Faqeih; Fowzan S Alkuraya; Matthew D Layne; Nazli B McDonnell; Paldeep S Atwal
Journal:  Am J Hum Genet       Date:  2018-03-29       Impact factor: 11.025

10.  FACS-Seq analysis of Pax3-derived cells identifies non-myogenic lineages in the embryonic forelimb.

Authors:  Arun J Singh; Chih-Ning Chang; Hsiao-Yen Ma; Stephen A Ramsey; Theresa M Filtz; Chrissa Kioussi
Journal:  Sci Rep       Date:  2018-05-16       Impact factor: 4.379

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