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. 2017 Feb 7;8:28. doi: 10.1186/s13287-017-0479-4

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 8 — Laminin regulates ITGA7 expression in both type I and type II pericytes. a Western blots and quantification of integrin α7 (ITGA7; 120 kDa) expression in wild-type (WT) and laminin γ1^flox/flox:Pdgfrβ-Cre⁺(PKO) type I pericytes in the presence of saline (Sal) or laminin-111 (Ln). Actin was used as a loading control. n = 3. b Western blots and quantification of ITGA7 (120 kDa) expression in WT and PKO type II pericytes in the presence of Sal or Ln. Actin was used as a loading control. n = 3. Data are shown as mean ± SD. **p < 0.01 versus WT + Sal; ^# p < 0.05 versus PKO + Sal