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© The Rockefeller University Press, 0021-9525/2003/11/661 $8.00
The Journal of Cell Biology, Volume 163, Number 3, 661-671

MT1-MMP–dependent, apoptotic remodeling of unmineralized cartilage

Kenn Holmbeck¹, Paolo Bianco², Kali Chrysovergis¹, Susan Yamada¹ and Henning Birkedal-Hansen¹

¹ Matrix Metalloproteinase Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892
² Dipartimento di Medicina Sperimentale e Patologia, Universitá La Sapienza, Parco Scientifico Biomedico San Raffaele, 00161 Rome, Italy

Address correspondence to Henning Birkedal-Hansen, National Institute of Dental and Craniofacial Research, Building 30, Rm. 132, 30 Convent Dr., MSC 4326, National Institutes of Health, Bethesda, MD 20892. Tel.: (301) 496-1483. Fax: (301) 402-1512. email: hbhansen{at}dir.nidcr.nih.gov

Skeletal tissues develop either by intramembranous ossification, where bone is formed within a soft connective tissue, or by endochondral ossification. The latter proceeds via cartilage anlagen, which through hypertrophy, mineralization, and partial resorption ultimately provides scaffolding for bone formation. Here, we describe a novel and essential mechanism governing remodeling of unmineralized cartilage anlagen into membranous bone, as well as tendons and ligaments. Membrane-type 1 matrix metalloproteinase (MT1-MMP)–dependent dissolution of unmineralized cartilages, coupled with apoptosis of nonhypertrophic chondrocytes, mediates remodeling of these cartilages into other tissues. The MT1-MMP deficiency disrupts this process and uncouples apoptotic demise of chondrocytes and cartilage degradation, resulting in the persistence of "ghost" cartilages with adverse effects on skeletal integrity. Some cells entrapped in these ghost cartilages escape apoptosis, maintain DNA synthesis, and assume phenotypes normally found in the tissues replacing unmineralized cartilages. The coordinated apoptosis and matrix metalloproteinase-directed cartilage dissolution is akin to metamorphosis and may thus represent its evolutionary legacy in mammals.

Key Words: cranial vault; Meckel's cartilage; matrix dissolution; chondrocyte apoptosis; metamorphosis; MT1-MMP

Abbreviations used in this paper: MC, Meckel's cartilage; MMP, matrix metalloproteinase; MT1-MMP, membrane-type 1 MMP.

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