Abstract
Paraffin sections of human skeletal tissues were studied in order to identify cells responsible for production of types I, II, and III collagens by in situ hybridization. Northern hybridization and sequence information were used to select restriction fragments of cDNA clones for the corresponding mRNAs to obtain probes with a minimum of cross- hybridization. The specificity of the probes was proven in hybridizations to sections of developing fingers: osteoblasts and chondrocytes, known to produce only one type of fibrillar collagen each (I and II, respectively) were only recognized by the corresponding cDNA probes. Smooth connective tissues exhibited variable hybridization intensities with types I and III collagen cDNA probes. The technique was used to localize the activity of type II collagen production in the different zones of cartilage during the growth of long bones. Visual inspection and grain counting revealed the highest levels of pro alpha 1(II) collagen mRNAs in chondrocytes of the lower proliferative and upper hypertrophic zones of the growth plate cartilage. This finding was confirmed by Northern blotting of RNAs isolated from epiphyseal (resting) cartilage and from growth zone cartilage. Analysis of the osseochondral junction revealed virtually no overlap between hybridization patterns obtained with probes specific for type I and type II collagen mRNAs. Only a fraction of the chondrocytes in the degenerative zone were recognized by the pro alpha 1(II) collagen cDNA probe, and none by the type I collagen cDNA probe. In the mineralizing zone virtually all cells were recognized by the type I collagen cDNA probe, but only very few scattered cells appeared to contain type II collagen mRNA. These data indicate that in situ hybridization is a valuable tool for identification of connective tissue cells which are actively producing different types of collagens at the various stages of development, differentiation, and growth.
Full Text
The Full Text of this article is available as a PDF (3.2 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bernard M. P., Chu M. L., Myers J. C., Ramirez F., Eikenberry E. F., Prockop D. J. Nucleotide sequences of complementary deoxyribonucleic acids for the pro alpha 1 chain of human type I procollagen. Statistical evaluation of structures that are conserved during evolution. Biochemistry. 1983 Oct 25;22(22):5213–5223. doi: 10.1021/bi00291a023. [DOI] [PubMed] [Google Scholar]
- Bernard M. P., Myers J. C., Chu M. L., Ramirez F., Eikenberry E. F., Prockop D. J. Structure of a cDNA for the pro alpha 2 chain of human type I procollagen. Comparison with chick cDNA for pro alpha 2(I) identifies structurally conserved features of the protein and the gene. Biochemistry. 1983 Mar 1;22(5):1139–1145. doi: 10.1021/bi00274a023. [DOI] [PubMed] [Google Scholar]
- Brahic M., Haase A. T. Detection of viral sequences of low reiteration frequency by in situ hybridization. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6125–6129. doi: 10.1073/pnas.75.12.6125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheah K. S. Collagen genes and inherited connective tissue disease. Biochem J. 1985 Jul 15;229(2):287–303. doi: 10.1042/bj2290287. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheah K. S., Stoker N. G., Griffin J. R., Grosveld F. G., Solomon E. Identification and characterization of the human type II collagen gene (COL2A1). Proc Natl Acad Sci U S A. 1985 May;82(9):2555–2559. doi: 10.1073/pnas.82.9.2555. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denhardt D. T. A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun. 1966 Jun 13;23(5):641–646. doi: 10.1016/0006-291x(66)90447-5. [DOI] [PubMed] [Google Scholar]
- Edwards M. K., Wood W. B. Location of specific messenger RNAs in Caenorhabditis elegans by cytological hybridization. Dev Biol. 1983 Jun;97(2):375–390. doi: 10.1016/0012-1606(83)90094-5. [DOI] [PubMed] [Google Scholar]
- Elima K., Mäkelä J. K., Vuorio T., Kauppinen S., Knowles J., Vuorio E. Construction and identification of a cDNA clone for human type II procollagen mRNA. Biochem J. 1985 Jul 1;229(1):183–188. doi: 10.1042/bj2290183. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Focht R. J., Adams S. L. Tissue specificity of type I collagen gene expression is determined at both transcriptional and post-transcriptional levels. Mol Cell Biol. 1984 Sep;4(9):1843–1852. doi: 10.1128/mcb.4.9.1843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gay S., Müller P. K., Lemmen C., Remberger K., Matzen K., Kühn K. Immunohistological study on collagen in cartilage-bone metamorphosis and degenerative osteoarthrosis. Klin Wochenschr. 1976 Oct 15;54(20):969–976. doi: 10.1007/BF01468947. [DOI] [PubMed] [Google Scholar]
- Hayashi M., Ninomiya Y., Parsons J., Hayashi K., Olsen B. R., Trelstad R. L. Differential localization of mRNAs of collagen types I and II in chick fibroblasts, chondrocytes, and corneal cells by in situ hybridization using cDNA probes. J Cell Biol. 1986 Jun;102(6):2302–2309. doi: 10.1083/jcb.102.6.2302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kosher R. A., Kulyk W. M., Gay S. W. Collagen gene expression during limb cartilage differentiation. J Cell Biol. 1986 Apr;102(4):1151–1156. doi: 10.1083/jcb.102.4.1151. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kravis D., Upholt W. B. Quantitation of type II procollagen mRNA levels during chick limb cartilage differentiation. Dev Biol. 1985 Mar;108(1):164–172. doi: 10.1016/0012-1606(85)90018-1. [DOI] [PubMed] [Google Scholar]
- Loidl H. R., Brinker J. M., May M., Pihlajaniemi T., Morrow S., Rosenbloom J., Myers J. C. Molecular cloning and carboxyl-propeptide analysis of human type III procollagen. Nucleic Acids Res. 1984 Dec 21;12(24):9383–9394. doi: 10.1093/nar/12.24.9383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKibbin B. The biology of fracture healing in long bones. J Bone Joint Surg Br. 1978 May;60-B(2):150–162. doi: 10.1302/0301-620X.60B2.350882. [DOI] [PubMed] [Google Scholar]
- Moench T. R., Gendelman H. E., Clements J. E., Narayan O., Griffin D. E. Efficiency of in situ hybridization as a function of probe size and fixation technique. J Virol Methods. 1985 Jun;11(2):119–130. doi: 10.1016/0166-0934(85)90035-7. [DOI] [PubMed] [Google Scholar]
- Poole A. R., Pidoux I., Reiner A., Choi H., Rosenberg L. C. Association of an extracellular protein (chondrocalcin) with the calcification of cartilage in endochondral bone formation. J Cell Biol. 1984 Jan;98(1):54–65. doi: 10.1083/jcb.98.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raghow R., Gossage D., Seyer J. M., Kang A. H. Transcriptional regulation of type I collagen genes in cultured fibroblasts by a factor isolated from thioacetamide-induced fibrotic rat liver. J Biol Chem. 1984 Oct 25;259(20):12718–12723. [PubMed] [Google Scholar]
- Reddi A. H. Cell biology and biochemistry of endochondral bone development. Coll Relat Res. 1981 Feb;1(2):209–226. doi: 10.1016/s0174-173x(81)80021-0. [DOI] [PubMed] [Google Scholar]
- Rowe D. W., Moen R. C., Davidson J. M., Byers P. H., Bornstein P., Palmiter R. D. Correlation of procollagen mRNA levels in normal and transformed chick embryo fibroblasts with different rates of procollagen synthesis. Biochemistry. 1978 May 2;17(9):1581–1590. doi: 10.1021/bi00602a001. [DOI] [PubMed] [Google Scholar]
- Schmid T. M., Linsenmayer T. F. Immunohistochemical localization of short chain cartilage collagen (type X) in avian tissues. J Cell Biol. 1985 Feb;100(2):598–605. doi: 10.1083/jcb.100.2.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stanescu V., Stanescu R., Maroteaux P. Pathogenic mechanisms in osteochondrodysplasias. J Bone Joint Surg Am. 1984 Jul;66(6):817–836. doi: 10.2106/00004623-198466060-00002. [DOI] [PubMed] [Google Scholar]
- Stocum D. L., Davis R. M., Leger M., Conrad H. E. Development of the tibiotarsus in the chick embryo: biosynthetic activities of histologically distinct regions. J Embryol Exp Morphol. 1979 Dec;54:155–170. [PubMed] [Google Scholar]
- Stoker N. G., Cheah K. S., Griffin J. R., Pope F. M., Solomon E. A highly polymorphic region 3' to the human type II collagen gene. Nucleic Acids Res. 1985 Jul 11;13(13):4613–4622. doi: 10.1093/nar/13.13.4613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Syrjänen S., Syrjänen K., Mäntyjärvi R., Parkkinen S., Väyrynen M., Saarikoski S., Castren O. Human papillomavirus (HPV) DNA sequences demonstrated by in situ DNA hybridization in serial paraffin-embedded cervical biopsies. Arch Gynecol. 1986;239(1):39–48. doi: 10.1007/BF02134287. [DOI] [PubMed] [Google Scholar]
- Thomas P. S. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201–5205. doi: 10.1073/pnas.77.9.5201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van der Rest M., Rosenberg L. C., Olsen B. R., Poole A. R. Chondrocalcin is identical with the C-propeptide of type II procollagen. Biochem J. 1986 Aug 1;237(3):923–925. doi: 10.1042/bj2370923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vuorio E., Elima K., Pulkkinen J., Viitanen A. M. Identification of messenger RNA for human type II collagen. FEBS Lett. 1984 Sep 3;174(2):238–242. doi: 10.1016/0014-5793(84)81165-5. [DOI] [PubMed] [Google Scholar]
- Vuorio T., Mäkelä J. K., Vuorio E. Activation of type I collagen genes in cultured scleroderma fibroblasts. J Cell Biochem. 1985;28(2):105–113. doi: 10.1002/jcb.240280204. [DOI] [PubMed] [Google Scholar]
- von der Mark K. Immunological studies on collagen type transition in chondrogenesis. Curr Top Dev Biol. 1980;14(Pt 2):199–225. doi: 10.1016/s0070-2153(08)60195-7. [DOI] [PubMed] [Google Scholar]
- von der Mark K., von der Mark H. The role of three genetically distinct collagen types in endochondral ossification and calcification of cartilage. J Bone Joint Surg Br. 1977 Nov;59-B(4):458–464. doi: 10.1302/0301-620X.59B4.72756. [DOI] [PubMed] [Google Scholar]