A rapid and ultrasensitive method for measurement of DNA, calcium and protein content, and alkaline phosphatase activity of chondrocyte cultures

Cristina Teixeira, M. Hatori, P. S. Leboy, M. Pacifici, I. M. Shapiro

Research output: Contribution to journalArticle

Abstract

Most investigators are cognizant of the problems inherent in counting cells embedded in a complex and abundant extracellular matrix. To overcome these obstacles, we developed a new method of isolating nucleic acids from chondrocytes which facilitates measurement of cell number by DNA analysis. Chondrocytes were isolated from chick embryo sterna and grown continuously without subculturing for 2-3 weeks in monolayer. The cells were treated with triton X-100 and the nucleic acid content of the extract was determined by measuring DNA fluorescence in the presence of Hoechst dye 33258. To minimize background fluorescence due to the triton, we precipitated the DNA with alcohol and then solubilized the nucleic acids in EDTA. This simple procedure removed the detergent and substantially increased the sensitivity of the method. Thus, we could measure with high precision and high recovery, the DNA content of cultures of 10,000-50,000 cells. In a single well containing 0.5-1.0 million cells, sufficient material remained for subsequent measurements of alkaline phosphatase activity and protein and calcium content. As the mineral present in the triton-treated samples was soluble in EDTA, we experienced no problems in measuring the calcium content of the culture. In addition, as triton X-100 is a nonionic detergent, we were able to measure cell and matrix proteins; moreover, the presence of the triton maintained the catalytic state of alkaline phosphatase. We conclude that this procedure provides a simple and rapid approach to measuring major indicators of chondrocyte maturation and function.

Original languageEnglish (US)
Pages (from-to)252-256
Number of pages5
JournalCalcified Tissue International
Volume56
Issue number3
DOIs
StatePublished - Mar 1995

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Phosphoprotein Phosphatases
Chondrocytes
Alkaline Phosphatase
Calcium
DNA
Nucleic Acids
Octoxynol
Edetic Acid
Detergents
Fluorescence
Bisbenzimidazole
Sternum
Chick Embryo
Extracellular Matrix
Minerals
Proteins
Coloring Agents
Cell Count
Alcohols
Research Personnel

Keywords

  • Alkaline phosphatase
  • Chondrocytes
  • DNA analysis
  • Hoechst dye
  • Mineralization

ASJC Scopus subject areas

  • Endocrinology

Cite this

A rapid and ultrasensitive method for measurement of DNA, calcium and protein content, and alkaline phosphatase activity of chondrocyte cultures. / Teixeira, Cristina; Hatori, M.; Leboy, P. S.; Pacifici, M.; Shapiro, I. M.

In: Calcified Tissue International, Vol. 56, No. 3, 03.1995, p. 252-256.

Research output: Contribution to journalArticle

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AU - Shapiro, I. M.

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