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Published on: December 23, 2014
Identification of haemopoietic biglycan in hyperplastic thymus associated with myasthenia gravis
H Tomoyasu1, A Kikuchi, I Kamo
1Toranomon Hospital, Tokyo, Japan.
Insights
Biglycan, a key protein, promotes monocytic cell growth and differentiation. Its presence in hyperplastic thymuses suggests a role in myasthenia gravis pathogenesis.
Area of Science:
- Immunology
- Cell Biology
- Proteoglycan Research
Background:
- Biglycan typically functions in the extracellular matrix and as a factor reservoir.
- Recent findings indicate soluble biglycan stimulates monocytic cell growth and differentiation.
Purpose of the Study:
- To investigate the biological role of biglycan in human myasthenia gravis.
- To determine if biglycan is associated with thymic hyperplasia in myasthenia gravis patients.
Main Methods:
- Immunohistochemistry was used to detect biglycan in surgically removed thymuses.
- Biglycan was purified from hyperplastic thymuses using an immunoaffinity column.
- The effect of purified biglycan on monocytic cell differentiation was assessed using haemopoietic stem cells.
Main Results:
- Biglycan-positive cells were abundant in germinal centers of hyperplastic thymuses but absent in thymomas.
- Purified biglycan from hyperplastic thymuses existed as monomers and oligomers.
- Purified biglycan significantly stimulated monocytic cell growth and differentiation.
Conclusions:
- Specific biglycan-producing cells may be involved in the development and maintenance of thymic hyperplasia in myasthenia gravis.
- Biglycan's role extends beyond extracellular matrix functions, impacting immune cell development.
Abstract:
Generally biglycan, a small proteoglycan, has been thought to play a role as an extracellular matrix and/or a reservoir for other factors, such as TGF-beta and collagens. Recently, we have found that a soluble 100 kDa biglycan, produced from the rat thymic myoid cells and the brain glial cells, predominantly stimulates growth and differentiation of monocytic lineage cells from various lymphatic organs, including microglias. In the present study, we attempted to identify biological significance of the corresponding molecules in human, using five myasthenic thymuses (three with hyperplasia and two with thymoma) that had been surgically removed for therapeutic purpose. With immunohistochemistry, many biglycan positive cells were detected in the germinal center of the three hyperplastic thymuses, but not in the two thymuses associated with lymphocytic thymoma. Biglycan purified from the hyperplastic thymuses by an immunoaffinity column was found as a monomer with apparent molecular size of 95-100 kDa and self associated oligomers of greater than 201 kDa. The purified biglycan markedly stimulated the growth and differentiation of monocytic cells from haemopoietic stem cells of the rat bone marrow. These results suggest that particular cells, which produce haemopoietic biglycan, play significant roles in generation and maintenance of the hyperplastic changes associated with myasthenia gravis.
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