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Schwann cells induce cancer cell dispersion and invasion
Sylvie Deborde, … , Alan Hall, Richard J. Wong
Sylvie Deborde, … , Alan Hall, Richard J. Wong
Published March 21, 2016
Citation Information: J Clin Invest. 2016;126(4):1538-1554. https://doi.org/10.1172/JCI82658.
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Research Article Cell biology Oncology

Schwann cells induce cancer cell dispersion and invasion

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Abstract

Nerves enable cancer progression, as cancers have been shown to extend along nerves through the process of perineural invasion, which carries a poor prognosis. Furthermore, the innervation of some cancers promotes growth and metastases. It remains unclear, however, how nerves mechanistically contribute to cancer progression. Here, we demonstrated that Schwann cells promote cancer invasion through direct cancer cell contact. Histological evaluation of murine and human cancer specimens with perineural invasion uncovered a subpopulation of Schwann cells that associates with cancer cells. Coculture of cancer cells with dorsal root ganglion extracts revealed that Schwann cells direct cancer cells to migrate toward nerves and promote invasion in a contact-dependent manner. Upon contact, Schwann cells induced the formation of cancer cell protrusions in their direction and intercalated between the cancer cells, leading to cancer cell dispersion. The formation of these processes was dependent on Schwann cell expression of neural cell adhesion molecule 1 (NCAM1) and ultimately promoted perineural invasion. Moreover, NCAM1-deficient mice showed decreased neural invasion and less paralysis. Such Schwann cell behavior reflects normal Schwann cell programs that are typically activated in nerve repair but are instead exploited by cancer cells to promote perineural invasion and cancer progression.

Authors

Sylvie Deborde, Tatiana Omelchenko, Anna Lyubchik, Yi Zhou, Shizhi He, William F. McNamara, Natalya Chernichenko, Sei-Young Lee, Fernando Barajas, Chun-Hao Chen, Richard L. Bakst, Efsevia Vakiani, Shuangba He, Alan Hall, Richard J. Wong

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Figure 3

Schwann cells recruit cancer cells to DRG neurites.

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Schwann cells recruit cancer cells to DRG neurites.
(A) Coculture of DRG...
(A) Coculture of DRGs with MiaPaCa-2 F-RFP cells. Images from a time-lapse video showing progression of a cancer cell (marked by an asterisk) toward the center of the DRG (see Supplemental Video 1A). Times are shown as hours and minutes. (B) Cancer cells in contact with DRGs move faster than those not in contact. Quantification of the instantaneous velocity of MiaPaCa-2 cells without (n = 7) and with (n = 5) DRG contact. Data represent mean ± SEM. ****P < 0.0001, Mann Whitney test. (C) Association of Schwann cells with cancer cells on DRGs. Confocal image of a coculture of DRGs and MiaPaCa-2 F-RFP (red) cells immunostained for GFAP (green) and Tuj1 (blue), showing a Schwann cell with protrusions surrounding MiaPaCa-2 cells. The arrow marks a neuron element and the arrowhead marks a Schwann cell. (D and E) Images from time-lapse videos showing dynamic interactions between cancer cells and Schwann cells: (D) a cancer cell (marked by an asterisk) moving along Schwann cells (see Supplemental Video 1B) and (E) a DRG projection bridged (inset 1) or not bridged (inset 2) via Schwann cells to a cancer cell. Time-lapse images corresponding to inset 1 show cancer cell recruitment to the DRG. Time-lapse images corresponding to inset 2 show absence of cancer cell recruitment to the DRG. The arrow shows a protrusion developing from a cancer cell at a contact point with a Schwann cell. Times are shown as hours and minutes (see Supplemental Video 1, C and D). (F) Quantification of directionality of cancer cell movements corresponding to time-lapse videos shown in E after tracking cells over 24 hours, showing unidirectional migration by cancer cells toward their associated Schwann cells (top) (n = 6 cells) and random migration of cancer cells not associated with Schwann cells (bottom) (n = 8 cells). Scale bar: 100 μm.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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