Fibrillin-1 in the Vasculature

In Vivo Accumulation of eGFP-Tagged Fibrillin-1 in a Knockin Mouse Model

Noe L. Charbonneau, Elise C. Manalo, Sara F. Tufa, Eric J. Carlson, Valerie M. Carlberg, Douglas R. Keene, Lynn Sakai

Research output: Contribution to journalArticle

Abstract

Immunolocalization studies have shown that fibrillin-1 is distributed ubiquitously in the connective tissue space from early embryonic times through old age. When mutated, the gene for fibrillin-1 (FBN1) causes the Marfan syndrome, a common inherited disorder of connective tissue. The multiple manifestations of the Marfan syndrome reflect the known distribution of fibrillin-1 in cardiovascular, musculoskeletal, ocular, and dermal tissues. In this study, a mouse model of Marfan syndrome in which fibrillin-1 is truncated and tagged with green fluorescence was used to estimate the relative abundance of fibrillin-1 in developing tissues. In embryonic tissues, the aorta was the only tissue in which fibrillin-1 green fluorescence was detectable. Other arteries gained detectable fibrillin-1 green fluorescence just after birth. Fibrillin-1 fluorescence was observed at later postnatal times in the lung, skin, perichondrium, tendon, and ocular tissues, while other tissues remained negative. These results indicated that tissues most affected in the Marfan syndrome are the tissues in which fibrillin-1 is most abundant. Focus was placed on the aorta, since aortic disease is life threatening in the Marfan syndrome and fibrillin-1 green fluorescence was most abundant in this tissue. Fibrillin-1 green fluorescence and immunostaining showed that fibrillin-1 is within aortic medial elastic lamellae. Endothelial-specific compared to smooth muscle-specific fibrillin-1 green fluorescence, together with light microscopic analyses of fragmentation of aortic elastic lamellae, demonstrated that smooth muscle cell mutated fibrillin-1 contributed most to progressive aortic fragmentation. However, these studies also indicated that other cells, possibly endothelial cells, also contribute to this aortic pathology. Anat Rec, 2019.

Original languageEnglish (US)
JournalAnatomical Record
DOIs
StatePublished - Jan 1 2019

Fingerprint

animal models
fluorescence
Fluorescence
Marfan Syndrome
aorta
connective tissues
smooth muscle
eyes
fragmentation
muscle
tissues
Fibrillin-1
tissue
Connective Tissue
Aorta
genetic disorders
tendons
skin (animal)
myocytes
arteries

Keywords

  • aorta
  • blood vessels
  • fibrillin
  • lung
  • Marfan syndrome

ASJC Scopus subject areas

  • Anatomy
  • Biotechnology
  • Histology
  • Ecology, Evolution, Behavior and Systematics

Cite this

Fibrillin-1 in the Vasculature : In Vivo Accumulation of eGFP-Tagged Fibrillin-1 in a Knockin Mouse Model. / Charbonneau, Noe L.; Manalo, Elise C.; Tufa, Sara F.; Carlson, Eric J.; Carlberg, Valerie M.; Keene, Douglas R.; Sakai, Lynn.

In: Anatomical Record, 01.01.2019.

Research output: Contribution to journalArticle

Charbonneau, Noe L. ; Manalo, Elise C. ; Tufa, Sara F. ; Carlson, Eric J. ; Carlberg, Valerie M. ; Keene, Douglas R. ; Sakai, Lynn. / Fibrillin-1 in the Vasculature : In Vivo Accumulation of eGFP-Tagged Fibrillin-1 in a Knockin Mouse Model. In: Anatomical Record. 2019.
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