Collagen fibrillogenesis in vitro: interaction of types I and V collagen regulates fibril diameter

Journal of Cell Science - Tập 95 Số 4 - Trang 649-657 - 1990
David E. Birk1, John M. Fitch2, Joanne Babiarz1, Kathleen J. Doane1, Thomas F. Linsenmayer2
1Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey 1 Department of Pathology’ , , Piscataway, new Jersey 08854, USA
2Tufts University Health Sciences Schools, 136 Harrison Avenue 2 Department of Anatomy and Cellular Biology , , Boston, MA 02111, USA

Tóm tắt

ABSTRACT

The small-diameter fibrils of the chick corneal stroma are heterotypic, composed of both collagen types I and V. This tissue has a high concentration of type V collagen relative to other type I-containing tissues with larger-diameter fibrils, suggesting that heterotypic interactions may have a regulatory role in the control of fibril diameter. The interactions of collagen types I and V were studied using an in vitro self-assembly system. Collagens were purified from lathyritic chick embryos in the presence of protease inhibitors. The type V collagen preparations contained higher molecular weight forms of the α1 (V) and α2(V) chains constituting 60-70% of the total. Rotary-shadow electron micrographs showed a persistence of a small, pepsin-sensitive terminal region in an amount consistent with that seen by electrophoresis. In vitro, this purified type V collagen formed thin fibrils with no apparent periodicity, while type I collagen fibrils had a broad distribution of large diameters. However, when type I collagen was mixed with increasing amounts of type V collagen a progressive and significant decrease in both the mean fibril diameter and the variance was observed for D periodic fibrils. The amino-terminal domain of the type V collagen molecule was required for this regulatory effect and in its absence little diameter reducing activity was observed. Electron microscopy using collagen type specific monoclonal antibodies demonstrated that the fibrils formed were heterotypic, containing both collagen types I and V. These data indicate that the interaction of type V with type I collagen is one mechanism modulating fibril diameter and is at least partially responsible for the regulation of collagen fibril formation.

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