Clonal analysis of bone marrow stromal cells in multiple exostotic chondrodysplasia and systemic osteoporosis: features of cell cloning efficiency

Cover Page

Cite item

Full Text

Abstract

We studied the clonal features of bone marrow stromal cells obtained by biopsy of the iliac wing of patients with systemic skeletal diseases: multiple exostotic chondrodysplasia (16 patients) and systemic osteoporosis (24 patients). The proliferative potential of cells was investigated, the main indicator of which is the efficiency of cloning. We analyzed the induction-morphogenetic relationship between the efficiency of cloning and biological inducers contained in the autologous and added suspension of bone marrow cells (the so-called feeder). The rapid growth and proliferation of exostoses in multiple exostotic chondrodysplasia is apparently due to both the increased proliferative activity of the cultured cells themselves, and (especially) the increase in the growth-stimulating effect of the autologous "feeder", which distinguishes fast-growing exostoses from the so-called calm ones, in which the proliferative activity itself cells are increased (but to a lesser extent), and no enhancement of the effect of the autofeed is detected. In systemic osteoporosis, a sharp decrease in the efficiency of cloning of the target cells themselves has been established, which is probably associated with a weakening of their colony-forming properties and / or a decrease in their number in the explanted suspension.

About the authors

E. M. Meerson

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Author for correspondence.
Email: info@eco-vector.com
Russian Federation, Moscow, Russia

B. K. Ilyin

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Email: info@eco-vector.com
Russian Federation, Moscow, Russia

B. H. Burdygin

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Email: info@eco-vector.com
Russian Federation, Moscow, Russia

C. C. Rodionova

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Email: info@eco-vector.com
Russian Federation, Moscow, Russia

L. V. Balberkin

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Email: info@eco-vector.com
Russian Federation, Moscow, Russia

S. I. Mitin

Central Institute of Traumatology and Orthopedics. N.N. Priorova

Email: info@eco-vector.com
Moscow, Russia

References

  1. Лурия Е.А., Оуэн М., Фриденштейн А.Я. и др. //Бюл. экспер. биол.— 1986.— № 4.— С. 481--483.
  2. Меерсон Е.М., Ильина В.К., Барер Ф.С. и др. //Ортопед, травматол.— 1990.— № 9.— С. 43 — 48.
  3. Терехов С.М. Клональный анализ при изучении наследственной
  4. патологии: Автореф. дис. ... канд. мед. наук.— М., 1984.
  5. Фриденштейн А.Я., Лалыкина КС. Индукция костной ткани и остеогенные клетки-предшественники.— М., 1973.
  6. Фриденштейн А.Я., Лурия Е.А. Клеточные основы кроветворного микроокружения.— М., 1980.
  7. Фриденштейн Ф.Я. //Методы клонирования клеток.—Л.,1988.—С. 257 — 265.
  8. Шапошников К).Г., Меерсон Е.М., Гринберг К.II. и др. //Генетические и иммунологические методы исследования больных с заболеваниями опорно-двигательного аппарата. М., 1988.— С. 3 — 10.
  9. Castro-Malaspina II. et al. //Blood.— 1980,—Vol. 56, № 2,— P. 289 — 301.
  10. Cristofalo V.J. //Senescence, Dominant or Recessive in Somatic All Crosses/Eds Nichols, Murphy.— New York; London, 1977.—P. 13 — 21.
  11. Hayflick L. //Handbook of the Biology of Aging./Eds C. Finch, L. Hayflick.—New York, 1977.—P. 159 —179.
  12. Hirota J., Okamura S., Kimura N et al. //Europ. J. Haemal.— 1988.—Vol. 40,—№ 1.—P. 83 — 90.

Copyright (c) 2022 Eco-Vector



This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies