Abstract
[6‐14C]Arginine ([6‐14C]Arg) was used as an in vivo pulse label to study BALB/c murine LPC‐1 plasmacytoma synthesis and secretion of its tumour‐associated M component (IgG2a, k). With this isotope, an eight‐ to ten‐fold enhancement in the labelling of the γ globulin region and ten‐fold reduction in the albumin labelling were observed. Production and secretion of the M component was detected (within 30 min) after cell transfer. Only mice which received tumour cells showed significant labelling in the γ globulin region 24 hr after isotope injection. The labelling behaviour of the tumour M component correlated with the administered cell dose. The peak heights of radioactivity in the γ region increased with increments in cell number. When the percentage radioactivity diverted into M component was plotted as a function of cell dose, a linear relationship was noted. This study demonstrates the feasibility of using [6‐14C]Arg as a tool to follow the newly synthesized tumour‐associated protein, and provides a means of estimating tumour cell number.
Original language | English (US) |
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Pages (from-to) | 71-80 |
Number of pages | 10 |
Journal | Cell Proliferation |
Volume | 12 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1979 |
Externally published | Yes |
ASJC Scopus subject areas
- Cell Biology