“…The most important mechanisms involved in ICH injury consist of early hematoma growth, which is the accumulation of toxic blood components [4] that causes mechanical destruction or displacement, and peri-hematomal injury resulting mainly from the inflammation around the blood clot, contributing to delayed neuronal death [5,6]. Brain edema formation and BBB (blood-brain barrier) disruption, caused by both hematomal and peri-hematomal injuries, have also been reported to be an important component of brain injury after ICH [7][8][9][10][11][12]. Mesenchymal stem cells generated from murine or human adipose tissues have been well documented [13][14][15][16][17][18][19][20][21][22] and have been named as adipose-derived stem cells [14,15,19,20], adipose-derived adult stem cells [21], adipose derived stromal cells [16], adipose derived mesenchymal stem cells [18], adipose tissuederived stem cells [13], and adipose tissue stromal cells [17].…”