Abstract 4117: Defective quorum sensing in Ph+ ALL and identification of diffusible factors secreted by cells growing at high cell density

• Published in: Cancer research (Chicago, Ill.) Ill.), 2013-04, Vol.73 (8_Supplement), p.4117-4117
• Main Authors: Patel, Sapan J., Su, Dao, Clarkson, Bayard
• Format: Article
• Language: English
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/1538-7445.AM2013-4117

Quorum sensing (QS) is a generic term describing cell-cell communication and collective decision making by bacteria and social insects to regulate expression of specific genes controlling cell density and other properties in response to changes in nutrient supply or environment. QS also has a role in higher organisms in maintaining homeostasis, regulation of the immune system and behavior of cancer cell populations. CML is a classic example of a tumor which without effective therapy consistently undergoes malignant progression, replacing the chronic phase (CP) cells with undifferentiated blast cells. Like most other types of acute leukemia including Ph+ ALL, the CML blasts proliferate slower than either normal or CP CML stem/progenitor (S/P) cells and individual blasts have greatly reduced proliferative potential and cloning ability suggesting the leukemic blasts achieve dominance by functioning as an aberrant ecosystem subject to different regulatory mechanisms than normal or CP CML S/P cells. To see if QS is involved we selected a p190 bcr-abl driven pre-B cell line (ALL3) derived from the pleural fluid of a patient dying of Ph+ ALL. Unlike other established human or murine Bcr-Abl driven lines, ALL3 cells don't form colonies or grow at low cell densities (LD) but grow progressively faster at increasing densities (HD). The cells are unresponsive to any known cytokines or combinations at any density. ALL3 cells at HD in upper inserts of transwells stimulate growth of LD cells in lower wells and LD ALL3 are also stimulated to grow by diffusible factors in the supernate (SN) of HD cells. Unstimulated LD ALL3 maintain fair viability (Trypan blue exclusion) for several days, and cells are also poised to begin proliferating; almost 98-100% are Ki-67+ and ∼40% incorporate BrdU, but an increasing number undergo apoptosis and only a minority regrow with addition of HD SN. The stimulatory factor(s) fail to stimulate other HD ALL3 cells, suggesting novel sensory circuits are activated upon population depletion or lack of close contact. LD ALL3 cells are also stimulated by SNs of enriched CD34+ cells at HD from normal PB, cord blood or CP CML but not by less enriched MNCs; it is not yet known if these stimulatory effects are due to the same or different factor(s). Our first objective is to identify the stimulatory protein(s) in the secretomes of HD ALL3 and other cells. The HD SN is stable upon storage at 4°C or -80°C with no loss of activity. Using cutoff filters a