NIME Next Batch PGI Quest in Delhi from 10 August to 20 August
A. Matrix metalloproteinase
B. TIMPs
C. SPARC
D. Mimecan
Not a component of inter photo-receptor matrix?
A. Matrix metalloproteinase
B. TIMPs
C. SPARC
D. Mimecan
Ans. D. (Mimecan)
Explanation
• Mimecanlosteoglycin, isolated from
bone, was originally called osteoinductive factor and later renamed
mimecan/osteoglycin ). It belongs to a family of small leucine-rich
proteoglycans (SLRPs) that are secreted into the extracellular matrix.
•
SLRPs, abundant in the bonematrix, cartilage cells, and connective tissues, are
important for collagen fibrillogenesis, cellular growth, differentiation, and
migration.
•
The physiological functions of mimecan have not yet been fully understood.
•
Initial studies have shown that mimecan can induce ectopic bone formation;
subcutaneous implantation of mimecan plus TGF-13 type 1 or 2 into rats induces
bone formation at the implantation site.
• In
atherosclerotic lesions, mimecan mRNA was down-regulated in the media and
up-regulated in the activated endothelium and thick neointima, whereas the
protein accumulated in the front edge of migrating smooth muscle cells.
• More recently, both pro- and mature mimecan have been shown to regulate type
I collagen fibrillogenesis, and conversion of mimecan from the precursor to
mature form, through cleavage by BMP- 1, potentiates the ability of mimecan to
modulate the formation of collagen fibrils.
•
Osteonectin, also known as SPARC and BM-40, is a 43-kDa Ca2 binding
glycoprotein with complex biological functions.
• Osteonectin/SPARC is believed to regulate cell growth through interactions
with the extracellular matrix. Increased secretion of osteonectirilSPARC is
associated with endothelial cell injury in vitro and the inhibition of cell
spreading on collagen.
• It
can also induce cell rounding in cultured endothelial cells and fibroblasts.
OsteonectinlSPARC will associate directly with platelet-derived growth factor
(PDGF) and modulate its activity.
•
Osteonectin/SPARC is performing an important function in the retina. Before
more specific functions can be explored, some basic properties of the protein
need to be determined, such as its turnover in the macula versus peripheral
retina, possible feedback mechanisms that affect regulation of transcription,
its calcium binding activity, and which retinal cell type(s) may be
synthesizing it.
•
This preferential expression and secretion by the macula is rather unique and
may be of particular interest to macular degenerations.
•
Photoreceptor degeneration is followed by remodeling of both neuronal and glial
cells as well as the vasculature: Genetic evidence for tissue and vessel
remodeling in the retina is based on the overexpression of aquaporin 4, matrix
metalloproteinase 9, tissue inhibitor of metalloproteinase 3, and fibroblast
growth factor-1 (cluster 1).
•
Matrix metalloproteinases and their tissue inhibitors have been shown to be
involved in extracellular matrix remodeling in a variety of brain pathologies
including optic nerve inflammation.